cognitive performance, fatigue, emotional and
TRANSCRIPT
Cognitive performance, fatigue, emotional and physiological strains in
simulated long-duration flight missions
Eduardo Rosa1,, Eugene Lyskov
2, Mikael Grönkvist
5, Roger Kölegård
5, Nicklas Dahlström
4, 1
Igor Knez1, Robert Ljung
3, Johan Willander
1 2
1 Department of Psychology, University of Gävle, Gävle, Sweden 3
2 Centre for Musculoskeletal Research, Department of Occupational Health Sciences and 4
Psychology, University of Gävle, Sweden 5
3 Department of Environmental Psychology, University of Gävle, Gävle, Sweden 6
4 Lund University School of Aviation, Lund University, Lund, Sweden 7
5 Division of Environmental Physiology, Swedish Aerospace Physiology Center, KTH Royal Institute 8
of Technology, Stockholm, Sweden 9
10
* Correspondence: 11
Corresponding Author 12
Eduardo Rosa 13
Keywords: fatigue, heart rate variability, cognitive performance, emotions, long-duration 15
military missions 16
Abstract 17
Pilots in long-duration flight missions in single-seat aircrafts may be affected by fatigue. This study 18
determined associations between cognitive performance, emotions and physiological activation and 19
deactivation – measured by heart rate variability – in a simulated 11-hours flight mission in the 39 20
Gripen aircraft. Eleven participants volunteered for the study. Perceived fatigue was measured by the 21
Samn-Perelli Fatigue Index (SPFI). Cognitive performance and objective fatigue were measured by 22
non-executive and executive tasks. Emotions were assessed by the Circumplex Affect Space 23
instrument. Heart rate variability (HRV) was considered in relation to the cognitive battery test in 24
four time points – Hours 3, 5, 7, 9 – and their associations with emotional ratings. Results indicated 25
decrease in performance in the non-executive task after approximately seven hours. This result was 26
correlated with self-reported measures of fatigue. Heart rate variability, assessed by indices of 27
parasympathetic modulation – RMSSD, pNN50 and mean RR Interval – remained unchanged for 28
both non-executive and executive tasks over time. There were associations between increased 29
boredom as well as passiveness and decrease in stimulation as well as activeness, and increased 30
HRV. This suggests that a low self-regulatory effort for maintaining performance in these tasks in 31
these environmental conditions was required. Combined results indicate that pilots may be able to 32
adapt to environmental demands and fatigue in long-duration missions providing that low self-33
regulatory effort is prevalent. 34
35
Fatigue in long-duration flight missions
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This is a provisional file, not the final typeset article
1 Introduction 36
Military pilots operating in single-seat multirole fighter aircrafts are exposed to a demanding 37
cognitive work environment, implying intense physical and psychological stress and fatigue (Driskell 38
and Salas, 1991). In such environments, vigilance decrements, complacency and loss of situation 39
awareness have long been identified as issues related to the increasing levels of complexity in 40
automation and other human-machine system errors (Parasuraman et al. 1993; Endsley and Kiris, 41
1995; Parasuraman and Riley 1997). The continuous increasing complexity of information 42
processing coupled with the changing operational characteristics of missions are factors that might 43
affect the performance of fighter pilots. One particular change in operational characteristics of multi-44
role fighter aircrafts relates to the duration of flight missions. Flight durations can now be prolonged 45
due to modern fighter aircrafts’ engineering features and purposes of employment, e.g., air policing 46
operations aided by air-refuelling or missions comprising multiple stops can now last more than 6 47
hours (personal communication, June 2018). Hence, the importance in assessing fighter pilots’ 48
cognitive performance, emotional strains and physiological variations in present long-duration 49
missions is paramount. Addressing pilots’ process capacity within these environmental 50
characteristics can support the design of missions with extended flight time, where fatigue may act as 51
a contributing factor to overall pilot performance. 52
The main purpose of this study is to investigate the effects of long-duration missions on cognitive 53
performance, fatigue, emotional and physiological strains. We examined mental fatigue influence on 54
cardiovascular (CV) responses throughout four time points during the 12 hours experimental session. 55
We have analysed heart-rate variability (HRV) in relation to cognitive task performance measures, 56
self-reported measures of fatigue and CV associations with emotional states. 57
In the military aviation context, fatigue-related errors during daytime operations may induce 58
performance degradation when pilots are exposed to extended periods of flight duty (Neville et al., 59
1994). Recently, Rosa et al. (2020) suggested that performance degradation in single-seat aircrafts 60
may occur in tasks targeting arousal and sustained attention after approximately seven hours into the 61
mission. Corresponding self-reported measures of fatigue with performance in response times were 62
also observed. Another possible indication of performance measurement relates to emotional ratings. 63
Rosa et al., (under review) have suggested that positive emotional ratings decrease and negative 64
emotional ratings increase also after about seven hours in long-duration missions. 65
The complex interplay between cognitive, emotion and also physiological regulation of goal-directed 66
behaviour is supported by a joint cortico-subcortical neural circuit (Grol & Raedt, 2020). These 67
processes are related to each other for adaptability to changing environmental demands, and there is 68
an overlap of the central autonomic network and neural circuits that support cognitive and emotion 69
regulation processes (Thayer, Hansen, Saus-Rose, & Johnsen, 2009; Thayer & Lane, 2000). The 70
balance between the excitatory sympathetic and inhibitory parasympathetic activity subsystems of the 71
autonomous nervous system (ANS) often interact in an opposing fashion, yielding varying degrees of 72
physiological arousal (Grol & Raedt, 2020). During physical and psychological stress, activity of the 73
SNS prevails, generating physiological arousal that will help us to adapt to the challenge up front. 74
Conversely, during conditions in which safety and stability is prevalent, the PNS is dominant, 75
maintaining a lower degree of physiological arousal (Appelhans & Luecken, 2006). Parasympathetic 76
inputs to the heart affect heart rate, such as more parasympathetic input reflects in more pronounced 77
acceleration and deceleration and more variable intervals between heart beats, that is, higher HRV 78
(Segerstrom & Nes, 2007). In this sense, an optimal HRV level is usually associated with self-79
Fatigue in long-duration flight missions
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regulatory capacity, and adaptability or resilience according to changing environmental demands 80
(Beauchaine, 2001; Berntson et al., 2008; Shaffer, & Ginsberg, 2017). 81
HRV addresses neurocardiac function and variations reflect heart-brain interactions and dynamic – 82
usually non-linear – ANS processes (Shaffer, & Ginsberg, 2017). HRV differences throughout time 83
reflect regulation of interdependent regulatory systems – autonomic balance, blood pressure, gas 84
exchange, gut, heart and vascular tone – in assisting in the adaptation during environmental and 85
psychological challenging conditions (Shaffer, & Ginsberg, 2017). The variability of non-linear 86
systems is one of the mechanisms of physiological adaptation that help us to cope with uncertain and 87
changing environments (Beckers et al., 2006). 88
HRV has been used to investigate fatigue influence on mental effort and associated cardiovascular 89
responses in challenging circumstances (Wright, & Stewart, 2012). Mental effort may be divided into 90
‘task effort’ and ‘state effort’ (Mulder, 1986). Task effort relates the properties of the task itself (task 91
difficulty and associated amount of controlled processing required). State effort relates to the amount 92
of effort required to protect task performance from negative influences of fatigue, environmental 93
pressures, etc. 94
As per the principle of HRV levels associations with adaptability, HRV may indicate self-regulatory 95
efforts in overcoming fatigue, particularly when an individual is under stressful tasks that involve 96
high level of mental load (Gonzalez et al., 2017), either by increases in task effort or by increases in 97
state effort. The principal premise is that fatigue may increase, decrease or have no effect on effort 98
and cardiovascular responses, and this depends on the difficulty of the impending challenge (LaGory 99
et al., 2011) 100
Hence, from the cognitive perspective, when the individual believes that success in achieving tasks’ 101
goals is possible, he or she will exert compensatory (self-regulatory) efforts to overcome fatigue 102
effects, experiencing increased arousal. On the other hand, when the individual does not believe that 103
success in achieving tasks’ goals is possible, people will suppress efforts to overcome fatigue effect, 104
experiencing minimal CV arousal. Lastly, when the individual beliefs on the impossibility in 105
achieving tasks’ goals is reinforced by fatigue, he or she will employ low effort, also displaying 106
minimal CV arousal (LaGory et al., 2011). This is an interesting mechanism as it forms the basis for 107
the variety in CV response patterns in relation to fatigue in different environments. 108
Certain studies on fatigue indicate that HRV is positively associated with mental fatigue state, i.e., 109
HRV increases as mental fatigue state increases, depending on the type of tasks (Ahsberg et al., 110
2000; Zhang & Yu, 2010; Huang et al., 2018). Also, HRV appears to index self-regulatory effort 111
when individuals are fatigued, showing that a parasympathetically mediated system is associated 112
with self-regulation (Segerstrom & Nes, 2007). This means that HRV is elevated during high self-113
regulatory effort compared with low self-regulatory effort. Another study pointed that HRV was 114
significantly increased due to time-on-task (Fairclough & Houston, 2004), whereas a more recent 115
finding indicated that HRV negatively associated with mental fatigue, i.e., decrease in 116
parasympathetic activity (RMSSD and pNN50), due to time-on-task effects (Melo et al., 2017). Tran 117
et al. (2009), however, observed that parasympathetic modulation such as RMSSD and pNN50 118
remained stable as participants experienced fatigue in a simulated driving task addressing 119
alertness/arousal, suggesting that fatigue may be associated with increased in sympathetic arousal. 120
Other studies pointed that CV responses in fatigued individuals can vary greatly according to 121
individual characteristics and environmental conditions (LaGory et al., 2011; Nolte et al., 2008). 122
Fatigue in long-duration flight missions
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Previous studies have also indicated changes in HRV during emotion regulation processes. Emotion 123
regulation is an attempt to change the present moment emotional experiences, behavioural 124
expressions and physiological responses (Gross, 1998). Thus, emotions experienced when humans 125
interact with their environment are associated with varying degrees of physiological arousal 126
(Levenson, 2003). As mentioned, HRV is usually associated with self-regulatory capacity and 127
depends on the environmental conditions. In this sense, emotion regulation depends on the 128
individual’s ability to continuously adjust physiological arousal (Gross, 1998) in accordance with 129
situational demands. HRV is, then, a measure of the interplay between sympathetic and 130
parasympathetic activity, providing information about the capacity for regulated emotional responses 131
(Grol & Raedt, 2020). 132
In general, there is a lack of consensus in the literature regarding HRV results concerning fatigue, 133
cognitive task performance and emotions. It seems that type of tasks (non-executive and executive 134
tasks), time-on-task, individual experiences and environmental circumstances play a role in HRV 135
results, with varying conclusions regarding the role of sympathetic and parasympathetic activity 136
related to mental fatigue and emotions. 137
Hence, the understanding of activation of ANS in long-duration flight missions – and its association 138
with cognitive performance and emotional experiences – may contribute to an integral assessment of 139
the psychology of pilots’ performance in such complex environment. 140
Regarding cognitive performance, considering that our experiment design did not involve time-on-141
task but challenging environmental conditions (physical limitations, discomfort and performance of 142
cognitive battery test in different points in time), we expected that participants would become 143
fatigued while trying to sustain cognitive performance (increase in self-regulatory effort), reflecting 144
an increase in HRV over time. Hence, the predictions of increase in HRV over time refers to the 145
assumption that participants would view success when performing the tasks as possible, exerting self-146
regulatory efforts to overcome fatigue effects. 147
Regarding emotions, we assumed that participants’ HRV would be associated with emotional ratings, 148
reflecting the attempt to self-regulate emotions according to environmental pressure. 149
Exact predictions regarding CV measures were problematic to estipulate, given the difficulty in 150
stipulating how fatigued participants would be and how much effort they would be willing to employ 151
when performing the tasks. In spite of this limitation, we formulated the following hypotheses: 152
H1. Effort-related CV responses would reflect fatigue development, implying that higher HRV is 153
positively correlated with fatigue (increased parasympathetic activity), in both non-executive and 154
executive components of task performance. 155
H2. Effort-related CV responses is associated with emotional states, such that higher HRV is 156
negatively correlated with positive emotions, and positively correlated with negative emotions. 157
2 Methods 158
This study is part of a larger research project. The methods section in this study is in accordance with 159
at least one previous publication (Rosa et al., 2020) within the project concerning the effects of long-160
duration flight missions. This study complies with the Declaration of Helsinki and was approved by 161
the Medical Research Ethics Review Board, in Stockholm (approval no:2018/806-3). 162
Fatigue in long-duration flight missions
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2.1 Participants 163
Participants comprised of twelve healthy individuals, and consisted of 10 men and 2 women. Mean 164
(SD) age, height and body mass were 28.2 (± 6.0) years, 179 (± 6.8) cm, 79.5 (± 16.9) kg, 165
respectively. Informed consent was obtained prior to participation. Participants could stop the 166
experiment at any time if they wished to do so. 167
2.2 Study Design 168
Experiments were conducted at the Flight Physiological Centre in Linköping, Sweden. A high-169
fidelity Dynamic Flight Simulator – DFS (Wyle Laboratories Inc., El Segundo, CA) was used. It 170
comprises of a 9.1m radius centrifuge equipped with a 39Gripen flight simulator mimicking the 171
aircraft controls and models. The hardware comprises of, e.g., a Martin-Baker seat (Martin Baker 172
Aircraft Co. Ltd., Middlesex, UK), stick and throttle (Page Aerospace Ltd., Middlesex, UK), and G-173
valve/breathing regulator (PSU BRAG valve, Honeywell Aerospace, Yeovil, UK). The total duration 174
of the experiment was 12 consecutive hours – calculated from the first cognitive test battery until the 175
last cognitive task battery. Both these tests occurred in a computer outside the DFS. The total mission 176
time was, then, 11 hours, considered by the time participants were strapped inside the DFS. 177
Participants wore a full-coverage anti-G suit, helmet with a mask covering the mouth and nose 178
(116H; Saab Ltd.), life jacket fitted with a chest bladder for assisted positive pressure breathing and 179
gloves (for details see Eiken et al., 2007) throughout the total duration of the experiment. Participants 180
were strapped with a 6-point seat belt while in the DFS. Participants could urinate by using an in-181
flight aircrew urine bladder relief system (AMXDmax®, Omni Measurement Systems, Inc, Milton, 182
USA) (Figure 1). Food was limited to three energy bars, three protein bars. Water was limited to 183
1.5L for the duration of the experiment. Intake were ad libitum. Front- and back-facing cameras were 184
used to monitor participants actions. 185
186
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187
Figure 1. The gondola depicting a participant strapped in the 39Gripen seat simulator. Mask and 188
helmet were used uninterruptedly for 11 consecutive hours. Cognitive tests were presented on the 189
center screen head-down display. Emotional rating scale and self-reported measure scale of fatigue 190
was affixed in the upper right corner from the central display (not visible). 191
192
A within-subjects, repeated measures design was used. Dependent variables were cognitive test 193
performance, self-reported measures of fatigue and heart rate variability. Independent measure was 194
physiological load (fatigue development) up to the 12th hour of the experiment. Level of significance 195
was p < .05 for statistical differences for all analyses. Bonferroni multiple-comparison correction was 196
used as post-hoc analysis. 197
198
2.3 Measures 199
2.3.1 Fatigue 200
Self-reported data were collected by the 7-point Samn-Perelli Fatigue Index (Samn & Perelli, 1982). 201
2.3.2 Cognitive tasks 202
Five cognitive tasks were part of the cognitive test battery. These tasks are representative of pilots’ 203
cognitive processes in the flight operational environment. 204
Psychomotor Vigilance Task (PVT). This task is a response time (RT) task to stimuli presented at 205
random intervals. It addresses changes in arousal and sustained attention deterioration associated 206
Fatigue in long-duration flight missions
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with fatigue-related variations and time on task (Dinges & Powell, 1985). A blank screen is initially 207
presented, followed by fixation cross (200ms) in the center of the screen. Next, the fixation cross 208
disappears. Then, at random intervals, a red circle appears in the center of the screen. Participants’ 209
task was to respond to the appearance of the red circle as fast as possible by pressing the space bar on 210
a keyboard. Inter-stimulus interval varied between 2 to 12s. Response latency was recorded. The 211
duration of the task was set for 5 minutes. 212
Visual Search Task. This task assesses targeting saliency and contextual cueing (see Treisman, 213
1985; Eckstein, 2011; Emrich et al., 2009). A dispersed matrix of a set of letters (‘U’, ‘D’, ‘G’, ‘C’, 214
‘Q’ – distractors) and one of the letters (‘X’ or ‘O’ – target) is initially presented (randomly 10, 30 or 215
50 programmed screen load weight). Participants’ task was to quickly identify one of the two 216
randomly presented targets (‘X’ or ‘O’, between trials) among the distractors. Reaction time and 217
accuracy were recorded. The task comprised 36 trials and lasted approximately 3.5 minutes. 218
Match-to-sample Task. This task assesses pattern recognition and short-term memory (Lieberman et 219
al., 2002; Shurtleff et al., 1994). A 6 x 6 matrix of red and yellow checkerboard pattern appears on 220
the screen for 1000ms. It then disappears for 3500ms. Then, two matrices appear simultaneously next 221
to each other; the original and a second (similar) matrix. Participants’ task was to select the matrix 222
that matched the original sample. Response latency and accuracy of target detection were recorded. 223
The task comprised 30 trials and lasted approximately 3 minutes. 224
N-back Task. This task assesses working memory (Kane et al., 2007). Participants’ task was to 225
acknowledge whether the stimulus (a number) in the sequence matched the one that appeared n 226
(number of) items before. We used only numbers as a stimulus as this involves the communication 227
characteristics of flight environment. Three blocks were performed for each session, varying in 228
memory load; 1-back, 2-back and 3-back (number of items), in this order. Each stimulus (number) 229
appeared for 500ms. The inter-stimulus interval was 2000ms. Accuracy for each task was recorded. 230
The task contained 50 trials per block, which was equivalent to approximately 1.5min per n-back task 231
(all three tasks lasted, then, 5min30s). 232
Mental Rotation Task. This task assesses internal representation of an object in space as it involves 233
imagining analogue space representations (Shepard & Metzler, 1971; for a review, see Zacks, 2008). 234
First, two equal figures appeared on the screen at the same time. Participants’ task was to identify 235
whether the images were rotated or whether they were mirrored in relation to each other. Response 236
was done by pressing the left shift button to identify ‘rotated’, and right shift button to identify 237
‘mirrored’. Decision time was set to a maximum of 5s. Response latency and accuracy for choice 238
were recorded. The duration of the task was 3 minutes. 239
240
2.3.3 Emotions 241
Emotional experience was acquired and assessed by the Circumplex Affect Space (CAS) instrument 242
(Knez & Hygge, 2001; Larsen & Diener, 1992). Eight affect states are represented in a circle 243
comprised of eight octants (Figure 2). The horizontal axis depicts Pleasant (P) and Unpleasant (UP) 244
valences. The vertical axis depicts High Activation (HA) and Low Activation levels (LA). 245
The diagonal axes define another four valences, in which pleasant valences are on the right – 246
Activated Pleasant (AP), Pleasant (P) and Unactivated Pleasant (UAP), and unpleasant valences are 247
placed on the left – Unactivated Unpleasant (UAUP), Unactivated Pleasant (UP) and Activated 248
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Unpleasant (AUP). HA and LA levels have no valence; they vary in magnitude only. Note that affect 249
octants that oppose each other (180°) have an antagonist association. This defines the circumplex 250
structure of space. 251
252
253
Figure 2. The circumplex affect space depicting the two-dimensional structure of pleasure-254
displeasure (horizontal axis) and high-low levels of perceived activity (vertical axis). It has eight 255
affective states with two adjectives each. Plus and minus signs indicate positive or negative affect, 256
respectively. Adapted from Knez (2014) 257
258
Two adjectives were chosen to represent each of the eight valences. This is a short version of this 259
instrument (see Knez, 2014). Participants rated their emotional experiences using a 1-5 scale (from 260
‘little to not at all’ to ‘very much’) when answering the question ‘How do you feel right now?’. 261
262
2.3.4 Heart rate variability 263
Electrocardiogram measurements were recorded with ECG-monitor/cardiometer (Gould 6600 264
ECG/Biotech module, Valley View, OH, USA). Ag/AgCl Electrodes were attached in a precordial 5-265
lead arrangement (two electrodes placed under the left and right collarbones and three electrodes 266
placed in line on the left lower rib cage). Recordings were acquired every 0.005s (sample rate: 267
200Hz). HRV variables were extracted from the original ECG data – measured continuously – for 268
analysis. For the PVT task, the initial and last 120s were considered. For the Visual Search, Match-269
to-Sample and Rotation tasks, the last 120 seconds in each task were considered. For the N-back 270
tasks (1, 2, and 3-back), the whole 90s of the duration of each task was considered plus 15s before 271
the first (1-back) task, the overlapping 15s between 1-back and 2-back and between the 2-back and 3-272
back, and the 15s after the 3-back task (totalling 120s for each N-back task). 273
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The time-domain HRV indicators considered were root mean square of successive differences 274
(RMSSD), percentage of adjacent intervals that differ from each other by more than 50ms (pNN50), 275
and mean Inter-Beat-Intervals (RR intervals). Inter-beat intervals (IBIs) from ECG data were plotted 276
versus time for visual inspection and for editing, by means of linear interpolation, of abnormal and 277
ectopic beats. 278
Repeated measures analysis of variance (ANOVA) was performed on all dependent measures for the 279
for each cognitive test battery and for self-reported measures of fatigue, with test session as the 280
within-subject factor. Heart rate variability data were quantified as RMSSD, pNN50 and mean RR 281
Intervals. Then, HRV data was analysed via repeated measures ANOVA (cognitive task condition x 282
time of performance – Hour 3, 5, ,7, 9 only, when participants were inside the gondola). 283
Post hoc differences were established using Bonferroni multiple-comparison correction. The level of 284
significance was set at p < .05 for all analyses. A Pearson correlation (r) was performed to measure 285
the strength and direction of association between HRV variables and emotions. 286
Results of self-reported measures of fatigue and cognitive performance are similarly reported 287
elsewhere (Rosa et al., 2020). Similarly, results on emotions over time are reported elsewhere 288
(manuscript under review). These three results are summarized in the Results section. 289
290
2.4 Procedure 291
The experiment was performed during daytime for 12 consecutive hours. Of those 12 hours, the 292
experiment part that was conducted inside the DFS lasted 11 hours. 293
Participants arrived at 7:00am at the Flight Physiological Centre. The electrocardiograph electrodes 294
were fitted and electrocardiogram monitor was started. 295
The cognitive task battery and fatigue ratings were administered in six points in time; before entering 296
the DFS (hour 0), while inside the DFS (hour 3, hour 5, hour 7 and hour 9 – centrifuge stationary), 297
and after leaving the DFS (hour 12). Randomization between tasks was not programmed as to obtain 298
the same cognitive load for each task in each point in time and for every participant. 299
Ratings of self-perception of fatigue and emotional ratings were obtained after each cognitive test 300
battery. Ratings were obtained by reading the SPFI scale and the CAS – attached inside the DFS 301
gondola – and verbally stating the chosen index through the inter-communication system. 302
ECG data was recorded throughout the 11 hours while participants were inside the gondola. HRV 303
variables were considered in relation to the beginning and end of cognitive tasks, i.e., obtained HRV 304
results were synced with cognitive tasks’ timings for assessment of cognitive performance over time. 305
The four measurement points were Hours 3, 5, 7 and 9. Averaged HRV data was considered for 306
correlations with emotional ratings. 307
Participants could engage in ‘free flying’ in the simulator between the cognitive test batteries. 308
309
310
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Table I. The experimental protocol 311 312
Time Procedure Time Procedure
0700 Arrive 1440 Air refueling task
0715 Start/Briefing 1450 Free flying
0730 Undress 1500 Cognitive tests
0735 Height/Weight 1530 Self-reported measures
0740 Urine sampling 1530 Free flying
0750 Blood sampling 1540 Air refueling task
0800 Instrumentation (ECG) 1550 Free flying
0810 Dressing 1700 Cognitive tests
0830 Cognitive tests 1730 Self-reported measures
0845 Self-reported measures 1730 Free flying
0850 Sits in the DFS 1740 Air refueling task
0900 Flight simulation phase starts 1750 Free flying
0915 G-tolerance test without anti-G suit (spinning
centrifuge)
1800 Spatial Disorientation task
(spinning centrifuge)
0945 G-tolerance test with anti-G suit
(spinning centrifuge)
1900 G-tolerance test without anti-G suit
(spinning centrifuge)
1025 Spatial Disorientation task
(spinning centrifuge)
1930 G-tolerance test with anti-G suit
(spinning centrifuge)
1100 Cognitive tests
(start stationary centrifuge time)
2000 Flight simulation phase ends
1130 Self-reported measures 2000 Moving out from the DFS
1135 Free flying 2005 Undress
1240 Air refueling task 2010 Urine sampling
1250 Free flying 2020 Blood sampling
1300 Cognitive tests 2030 Cognitive tests
1330 Self-reported measures 2055 Self-reported measures/Debrief
1335 Free flying 2100 Weight/Release
313
3 Results 314
3.1 Fatigue 315
Self-reported fatigue increased over time, F(5, 50) = 11.66, p < .001, p2 = .53. Bonferroni post hoc 316
tests revealed a difference between Hour 0 and Hour 7 (p = .04, Mean difference 95% CI [-3.2, -317
.59]), between Hour 0 and Hour 9 (p = .02, Mean difference 95% CI [-3.78, -.21]) and between Hour 318
0 and Hour 12 (p = .002, Mean difference 95% CI [-3.74, -.80]). 319
320
3.2 Cognitive performance 321
Significant results on differences in accuracy or reaction time were not observed for high-order 322
cognitive tasks throughout the 12 hours period. 323
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PVT task results revealed increase response time over time, F(5, 50) = 7.87, p = .001, p2 = .44. 324
Bonferroni post hoc tests revealed that a difference occurred between Hour 0 and Hour 7 (p = .02, 325
Mean difference 95% CI [-75.6, -5.3]), between Hour 0 and Hour 9 (p = .01, Mean difference 95% 326
CI [-76.9, -7.8]) and between Hour 0 and Hour 12 (p = .01, Mean difference 95% CI [-38.04, -3.4]). 327
3.3 Emotions 328
Regarding positive valences, participants reported being significantly less peppy/enthusiastic and less 329
glad/cheerful over time, (F(5, 50) = 14.1, p < .001, p2 = .58; F(5, 50) = 8.4, p < .001, p
2 = .45, 330
respectively). Bonferroni post hoc tests for peppy/enthusiastic revealed a significant difference 331
between Hour 0 and Hour 7, Hour 0 and Hour 9 and Hour 0 and Hour 12, (p = .009, Mean difference 332
95% CI [0.35, 2.74]; p = .002, Mean difference 95% CI [0.57, 2.70]; p = .00, Mean difference 95% 333
CI [0.56, 2.89], respectively). Bonferroni post hoc tests for glad/cheerful revealed a difference 334
between Hour 0 and Hour 7 and between Hour 0 and Hour 9 (p = .02, Mean difference 95% CI [0.10, 335
2.43]); p = .05, Mean difference 95% CI 0.002, 2.18], respectively). 336
Regarding negative valences, participants reported being significantly more drowsy/bored over time 337
(F(5, 50) = 8.5, p < .001, p2 = .46). Bonferroni post hoc tests revealed a significant difference 338
between Hour 0 and Hour 7, Hour 0 and Hour 9 and Hour 0 and Hour 12, p = .001, Mean difference 339
95% CI [-2.77, -0.68]; p = .006, Mean difference 95% CI [-2.53, -0.37]; p = .003, Mean difference 340
95% CI [-2.31, -0.04], respectively). 341
High activation level results indicated that participants were significantly less active/stimulated over 342
time, F(5, 50) = 11.7, p < .001, p2 = .54. Significant differences disclosed by Bonferroni post hoc 343
tests were observed between Hour 0 and Hour 7, Hour 0 and Hour 9 and Hour 0 and Hour 12, p = 344
.005, Mean difference 95% CI [0.45, 2.82]), p = .001, Mean difference 95% CI [0.24, 2.84]); p = 345
.002, Mean difference 95% CI [0.57, 2.70], respectively). 346
Low activation levels results showed that participants were overall significantly more 347
passive/inactive over time, F(5, 50) = 4.17, p < .05 , p2 = .29. However, Bonferroni post hoc tests 348
did not show significant differences. 349
3.4 Heart rate variability and fatigue 350
A Pearson’s correlation analysis showed no significant associations between RMSSD, pNN50 and 351
mean RR Interval and self-reported fatigue, r’ = 0.34, n = 10, p > .05; r’ = 0.29, n = 10, p > .05; r’ = 352
0.20, n = 10, p > .05, respectively. 353
3.5 Heart rate variability and cognitive performance 354
RMSSD results for all tasks were not significant as a function of time, p > .05. pNN50 results were 355
non-significant for all tasks as a function of time, p > .05, except for the 2-back task, F(3, 27) = 3.25, 356
p = .03, p2 = .26. Mean RR Intervals were not significant for all tasks as a function of time, p > .05. 357
Multiple comparisons with Bonferroni adjustments revealed non-significant differences in RMSSD, 358
pNN50 and mean RR Intervals over time for all tasks (Table 2). 359
360
361
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362
Table 2. Descriptive values (Mean (SD)) for HRV measures for the cognitive tasks in Hour 3, 5, 7 and 9 while 363 participants were inside the gondola in the DFS. 364
365 DFS phase
Hour 3 Hour 5 Hour 7 Hour 9
Mean (SD) Mean (SD) Mean (SD) Mean (SD) p
PVT (first 120s)
RMSSD 48.5 (25.7) 52.0 (22.0) 50.0 (29.5) 52.2 (30.1) 0.92
pNN50 13.2 (11.2) 11.0 (7.9) 11.8 (10.2) 12.5 (9.5) 0.48
RR Interval 0.84 (.13) .81 (.12) .83 (.17) .84 (.14) 0.64
PVT (last 120s)
RMSSD 46.1 (24.1) 50.5 (23.5) 48.2 (27.5) 47.2 (28.0) 0.65
pNN50 11.3 (9.9) 10.2 (9.0) 12.4 (11.2) 10.2 (9.8) 0.42
RR Interval .85 (.13 .83 (.14) .83 (.17) .84 (.17) 0.66
Visual Search
RMSSD 44.6 (24.4) 48.4 (26.3) 44.5 (25.2) 47.3 29.5) 0.63
pNN50 10.2 (10.5) 10.6 (10.0) 9.9 (9.4) 11.0 (10.4) 0.58
RR Interval .83 (.13) .81 (.13) .82 (.16) .83 (.15) 0.62
Match-to-Sample
RMSSD 44.7 (24.2) 48.8 (27.4) 51.9 (29.9) 46.6 (26.1) 0.32
pNN50 10.1 (9.2) 10.8 (9.7) 11.1 (9.5) 10.7 (9.4) 0.92
RR Interval .82 (.12) .81 (.14) .81 (.16) .81 (.13) 0.96
1-back
RMSSD 54.1 (34.6) 45.7 (21.7) 44.6 (23.7) 45.9 26.6) 0.49
pNN50 9.5 (7.8) 8.6 (7.1) 10.4 (9.1) 10.0 (9.0) 0.43
RR Interval .80 (.10) .79 (.12) .80 (.17) .80 (.15) 0.94
2-back
RMSSD 40.5 (27.1) 46.3 (26.4) 47.3 25.9) 46.2 (28.8) 0.20
pNN50 7.8 (8.4) 10.8 (9.5) 9.5 (8.7) 10.6 (10.2) 0.03*
RR Interval .80 (.13) .80 (.12) .80 (.16) .82 (.15) 0.80
3-back
RMSSD 39.7 (22.2) 41.3 (18.7) 44.3 (25.0) 43.4 (31.1) 0.73
pNN50 8.4 (9.1) 7.8 (6.4) 10.0 (9.2) 9.9 (10.2) 0.34
RR Interval .81 (.14) .79 (.12) .80 (.16) .83 (.18) 0.51
Mental rotation
RMSSD 47 (28.7) 39.7 (19.7) 42 (26.2) 45.5 (31.9) 0.21
pNN50 9.7 (9.9) 9.1 (8.6) 9.0 (8.9) 10.6 (10.6) 0.59
RR Interval .83 (.14) .80 (.15) .81 (.19) .82 (.17) 0.37
Note: ª N=10 due to data loss
* Bonferroni post hoc test revealed NS results
366
3.6 Heart rate variability and emotions 367
Overall results of the Pearson correlation are depicted in Table 3. HRV variables significantly 368
correlated with each other; RMSSD significantly correlated with pNN50, r’ = 0.98, n = 10, p < .01; 369
Fatigue in long-duration flight missions
13
RMSSD significantly correlated with mean RR Interval, r’ = 0.90, n = 10, p < .01; and pNN50 370
significantly correlated with mean RR Interval, r’ = 0.88, n = 10, p < .01). 371
3.6.1 RMSSD 372
Results of the Pearson correlation indicated that there was a significant positive association between 373
the negative valence drowsy/bored, as well as the LA level passive/inactive and RMSSD (r’ = 0.69, n 374
= 10, p < .05; r’ = 0.79, n = 10, p < .01, respectively). There was a significant negative association 375
between the positive valence glad/cheerful as well as the HA level active/stimulated and RMSSD (r’ 376
= -0.64, n = 10, p < .05; r’ = 0.78, n = 10, p < .01, respectively). 377
This indicates that as participants become more drowsy/bored, passive/inactive and less 378
active/stimulated, cheerful, RMSSD increases. 379
3.6.2 pNN50 380
Correspondingly to RMSSD results, there was a significant positive association between the LA level 381
passive/inactive and pNN50 (r’ = 0.76, n = 10, p < .01). The LA level passive/inactive revealed a 382
near significant association with pNN50 (r’ = 0.61, n = 10, p = .059). There was a significant 383
negative association between HA level active/stimulated and pNN50 (r’ = -0.74, n = 10, p < .05). 384
Similarly, we observed a near significant negative association between the positive valence 385
glad/cheerful and pNN50 (r’ = -0.61, n = 10, p = .057). 386
Interestedly, there was a negative association between the negative valence sad/gloomy and pNN50 387
(r’ = -0.65, n = 10, p < .05). 388
These results indicate that as participants became more passive/inactive, less active/stimulated, but 389
also less sad/gloomy, pNN50 increases. 390
3.6.3 RR Interval 391
Results considering the mean RR Interval revealed a significant positive association between the 392
negative valence drowsy/bored (r’ = 0.64, n = 10, p < .05). There was a significant negative 393
association between the positive valence calm/serene, the HA level active/stimulated and mean RR 394
Interval (r’ = -0.66, n = 10, p < .05; r’ = -0.71, n = 10, p < .05, respectively). 395
These results suggest that as participants became more drowsy/bored, less calm/serene and less 396
active/stimulated, mean RR interval increases, indicating increase in HRV. 397
Combined results of HRV measures and positive/negative valences of emotions suggest that there is 398
a correlation of being more drowsy/bored, and increased heart rate variability. Considering high/low 399
activation levels, results exhibited a correlation of being more passive/inactive, as well as less 400
active/stimulated and increased heart rate variability. 401
402
Table 3. Correlations between HRV variables considered (RMSSD, pNN50 and mean RR Interval) and the eight 403 emotional states. 404
405
Fatigue in long-duration flight missions
14
This is a provisional file, not the final typeset article
Table 3. Correlations between HRV variables considered (RMSSD, pNN50 and mean RR Interval) and the eight 406 emotional states. 407 408
Measures 1 2 3 4 5 6 7 8 9 10 11
1. RMSSD ⎻
2. pNN50 .987** ⎻
3. RR Interval .909** .889** ⎻
4. Peppy/enthusiastic -0.567 -0.469 -0.534 ⎻
5. Glad/cheerful -.648* -0.618 -0.52 .749* ⎻
6. Calm/serene -0.574 -0.528 -.667* 0.436 0.625 ⎻
7. Nervous/anxious -0.286 -0.393 -0.262 -0.576 -0.201 0 ⎻
8. Sad/gloomy -0.57 -.659* -0.546 0.004 0.289 0.329 0.56 ⎻
9. Drowsy/bored .694* 0.613 .643* -.867** -.696* -0.44 0.367 -0.207 ⎻
10.Active/stimulated -.782** -.745* -.712* .771** .811** 0.549 -0.21 0.329 -.774** ⎻
11. Passive/inactive .799** .765** 0.613 -.742* -.833** -0.412 0.045 -0.463 .832** -.784** ⎻
Note: N = 10 due to HRV data acquisition loss.
* Correlation is significant at the 0.05 level.
** Correlation is significant at the 0.01 level.
409 Table 3. Continued 410 411
Variables 1 2 3 4 5 6 7 8 9 10 11
M 46.461 10.325 0.8205 3.025 3.275 3.575 1.25 1.225 2.275 2.7 2.125
SD 24.30 8.97 0.14 0.58 0.65 0.87 0.37 0.30 0.66 0.62 0.83
412
4 Discussion 413
The purpose of this study was to examine physiological response to cognitive and emotional loads in 414
simulated long-duration flight missions. Hypothesis 1, stating that participants would exhibit increase 415
in variability while trying to sustain task performance as they become fatigued, was not confirmed. 416
Results from participants’ absolute RMSSD, pNN50 and mean RR Intervals referring to increase in 417
parasympathetic indices were shown to be stable while performing both non-executive and executive 418
tasks over time. Hypothesis 2, regarding emotions – stating that higher HRV is negatively correlated 419
with positive emotions, and positively correlated with negative emotions – was partially confirmed. 420
Considering the positive valences, i.e., peppy/enthusiastic, glad/cheerful and calm/serene, 421
glad/cheerful negatively correlated with RMSSD (near significance was observed with pNN50) and 422
calm/serene negatively associated with mean RR Interval. Concerning the negative valences, i.e., 423
nervous/anxiousness, sad/gloomy, drowsy/bored, drowsy/bored positively correlated with RMSSD 424
and mean RR Interval (near significance was observed for pNN50). Interestedly, in an opposing 425
direction, sad/gloomy was negatively associated with pNN50. As for high/low activation levels, i.e., 426
active/stimulated, passive/inactive, for which there was no hypothesis, active/stimulated negatively 427
correlated with RMSSD, pNN50 and mean RR Interval, whereas passive/inactive was positively 428
associated with RMSSD and pNN50. 429
Fatigue in long-duration flight missions
15
Additionally, participants reported significantly increased levels of fatigue after approximately seven 430
hours into the mission. This was shown by results from the self-reported measures of fatigue and the 431
significant performance decrease in sustained attention – as shown by decrease in performance by the 432
non-executive PVT task – around Hour 7. There was no support for the effect of fatigue on executive 433
tasks targeting saliency and contextual cueing, short-term memory, pattern recognition, working 434
memory and analog spatial representations. Participants were significantly less peppy/enthusiastic, 435
less glad/cheerful, less active/stimulated and more drowsy/bored and more passive/inactive also after 436
approximately 7 hours into the mission. 437
Regarding cognitive performance, previous associations between HRV and mental effort generally 438
revealed increased in CV arousal as mental effort increases. Self-regulatory effort may covary with 439
HRV, such that higher HRV may reflect greater self-regulatory effort (Segerstrom & Nes, 2007). In 440
this sense, it is expected higher HRV during high self-regulatory effort compared with low self-441
regulatory effort. Self-regulatory tasks are associated with activation of prefrontal cortex (PFC), and 442
self-regulatory fatigue affects cognitive task performance that are frontal or executive (Schmeichel et 443
al., 2003; Small et al., 2001). The central autonomic network (CAN) is in part responsible for 444
parasympathetic input to the heart (Ahern et al., 2001). Since the CAN and structures that are central 445
for self-regulation colocalize in the brain, cortical activities that follows self-regulation may also play 446
a role in increased vagal input to the heart. 447
Mulder (1986) divided mental effort in ‘task effort’ and ‘state effort’. In the present study, it might be 448
the case that task effort was low. The associated amount of controlled processing for performing the 449
executive tasks in our experiment might not have been demanding; tasks were not particularly hard to 450
perform. It might also be the case that ‘state effort’ was low. Similarly, the amount of effort required 451
to protect task performance from detrimental effects of fatigue or environmental pressures over time 452
also might have been low. This reasoning finds support in the observed non-significant performance 453
differences in accuracy and response times for the executive tasks over time. Also, no penalty was 454
implied if not performing well, which might have been a reason for a possible lower effort in 455
performing the tasks. 456
Considering this, it is possible to argue that individuals believed that success in achieving tasks’ 457
goals was possible, implying that recruitment of self-regulatory strength over time to maintain 458
performance was not required. This follows the arguments proposed by LaGory et al. (2011), in 459
which CV responses depends on the difficulty of the impeding challenge; stable indices of HRV and 460
observed sustained accuracy in performance suggest that mental effort, i.e., ‘task effort’ and ‘state 461
effort’, was low, indicating that participants were not vulnerable to the negative consequences of self-462
regulatory fatigue. As self-regulatory efforts are presumably associated with prefrontal cortex 463
activities, as well as influences of the CAN in controlling vagal inputs to the heart when self-464
regulation is present, as mentioned, unchanging HRV responses corroborates to the assumption that 465
maintaining performance as fatigue developed in these executive tasks did not infer self-regulation. 466
As per the non-executive task, i.e., PVT task, addressing sustained attention, our results are in line 467
with results from Tran et al. (2009). Parasympathetic modulation shown by RMSSD, pNN50 and 468
mean RR Interval indices remained stable from pre- to post task as individuals performed a similar 469
attention task. In the present experimental conditions, this occurred even after degradation of 470
performance in this task after approximately seven hours. The processing of the PVT task – a low-471
order processing task sensible to fatigue effects – is considered to occur in brain regions responsible 472
for attention and motor function, involving the frontoparietal sustained-attention network 473
(Drummond et al., 2005) – therefore different from executive tasks processed in the PFC. The 474
Fatigue in long-duration flight missions
16
This is a provisional file, not the final typeset article
recruitment of a different information processing network as compared to executive tasks indicates 475
that performance in the PVT task is not dependent on effort, hence the lack of observation in 476
differences in parasympathetic activity. This offers another description for the stable indices of 477
parasympathetic activity relative to this task. 478
Regarding emotions, nevertheless, these results are in line with previous findings over time in these 479
environmental conditions (manuscript under review), where emotionality ratings addressing 480
glad/cheerful significantly decreased after approximately 7 hours into the mission. Similarly, 481
emotions addressing drowsy/bored significantly increased after 7 hours and, following the same 482
trend, participants reported being less active/stimulated and more passive/inactive, also after around 483
hour 7. Here we find associations concerning these variables and increase in HRV. Increases in HRV 484
usually reflect self-regulatory capacity when individuals are fatigued, implying that a 485
parasympathetically mediated system is associated with self-regulation (Segerstrom & Nes, 2007). In 486
this study, emotional variables associated with increase in HRV were related to increased levels of 487
boredom and passiveness, and decreased levels of cheerfulness and stimulation. 488
A possible interpretation relates to a reduction of available energy resources after approximately 7 489
hours, reflected by a decrease of PVT task performance (decreased arousal). Prior consumption of 490
cognitive resources impaired emotion regulation. Grillon et al. (2015) suggested that depletion of 491
cognitive resources – or the extent to which resources is drained and recover over time – can impair 492
emotion regulation. Still, described associations between emotional ratings and increase in 493
parasympathetic activity when individuals were fatigued may be related to the environmental 494
conditions in the simulated mission, as the situation was safe and stable. This is in line with the 495
established consensus indicating that PNS is dominant when the individual is not subjected to high 496
levels of psychological stress (Appelhans & Luecken, 2006). Conversely, SNS exhibits long-term 497
dominance over the PNS when individuals are vulnerable to high stress levels, having detrimental 498
effects at psychological and physical dimensions (Pinna & Edwards, 2020). 499
In summary, effort-related CV responses were stable irrespective of fatigue development in executive 500
and non-executive tasks in simulated long-duration missions. The lack of significant differences in 501
HRV over time may be due to insufficient task demand to induce performance decrease in executive 502
tasks due to fatigue. This may also have occurred due to the repetitive nature of the battery test, 503
facilitating a practice effect. We find support for these assumptions since performance decrements in 504
these tasks over time were not observed. This is a limitation in this study. 505
These results demand careful interpretation as the three HRV variables significantly correlated with 506
each other. The premise that there might be low statistical power cannot be discarded, as the sample 507
size in this study is small and some results yielded moderate effect sizes concerning correlations of 508
emotional valences. Correlations concerning emotions varying in magnitude, i.e., the high/low 509
activation levels, on the other hand, yielded high correlation coefficients, and significant results were 510
observed between both ratings and all three HRV variables considered, except for passive/inactive 511
and mean RR Interval. 512
Considering this, it is important to notice that the results of executive tasks and emotional ratings 513
should not be taken detached from the present conditions, i.e., the simulated environment. It is 514
problematic to generalize that executive tasks are not affected by fatigue in other circumstances. 515
Rather, differences in performance in these tasks are not easy to detect, and depend on type of tasks, 516
environmental conditions and individual characteristics. Regarding the latter, another limitation in 517
this study relates to the observation of individuals who have a strong need to achieve versus 518
Fatigue in long-duration flight missions
17
individuals who do not. Probably, the first will have high levels of success importance in challenging 519
conditions. As such, they should be more likely to display CV responses differences in response to 520
fatigue compared to individuals who do not have a strong need to achieve. Since our sample 521
comprised of pilots and nonpilots – and pilots supposably would have higher will to perform in these 522
conditions compared to nonpilots – this difference may also have played a role in the non-significant 523
amplification of CV responses (and our sample was too small for a between-group comparisons). 524
Fatigue effects on HRV responses have been broadly different, with some studies reporting positive 525
effects, others reporting negative effects and others reporting null effects, as cited. Associations 526
between HRV and fatigue need careful consideration of type of tasks and environmental conditions. 527
Nevertheless, HR/HRV may be an instrument for assessing pilot’s performance in more realistic and 528
complex flight missions (Mansikka et al., 2016). 529
530
5 Conclusions 531
In this simulated long-duration mission environment, we did not observe differences in HRV in non-532
executive and executive task performance over time. This denotes that a low self-regulatory effort 533
was required for maintaining performance in executive tasks in these environmental conditions. 534
Relatedly, the non-executive task – being not dependent on effort – did not show associations with 535
increased HRV. 536
We observed associations between increased boredom as well as passiveness and decrease in 537
stimulation as well as activeness, and increased HRV. These results indicate a prevalence of 538
parasympathetic activity, reflecting a low degree of physiological arousal. Associations with these 539
emotional variables may relate to the fairly safe and stable conditions in this simulation. 540
Future research in this context might consider the investigation of CV responses during the 541
performance of simulated flight tasks. A collective investigation comprising HRV, cognitive 542
performance and emotions may enhance the understanding of the psychology of pilots in similar 543
conditions. Combined results indicate that pilots may be able to adapt to environmental demands and 544
fatigue in long-duration missions providing that low self-regulatory effort is prevalent. 545
546
6 Funding 547
The study was supported by the Swedish Armed Forces grant no 922:0918. 548
7 Conflicts of interest 549
The authors declare that the research was conducted in the absence of any commercial or financial 550
relationships that could be construed as a potential conflict of interest. 551
8 Ethics Approval 552
The Ethics Application was reviewed by the Medical Research Ethics Review Board – n° 2018/806–553
31, named “Fysiologiska och kognitiva effekter av långvariga flygpass i JAS39Gripen”. 554
Fatigue in long-duration flight missions
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This is a provisional file, not the final typeset article
9 Consent to participate 555
Informed consent was obtained from all individual participants included in the study. 556
10 Acknowledgements 557
We are grateful to the staff and engineers of the Dynamic Flight Simulator at the Flight Physiological 558
Center for their kind assistance in the study. 559
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