Spiritual Stress Responses
Spiritual Stress Responses
Spiritual Stress Responses
https://doi.org/10.1007/s10943-023-01819-2
ORIGINAL PAPER
Szabolcs Kéri1,2,3
Abstract
Individuals with a Religious or Spiritual Problem (RSP), as defined in the DSM-5,
experience distress associated with faith-related moral dilemmas, existential mean-
ing, and transpersonal attitudes toward other people. It is unclear whether a RSP
reflects a generally heightened stress reactivity or whether the stress response is con-
fined to religious and spiritual contexts. To elucidate this issue, we measured behav-
ioral and physiological responses during social-evaluative stress (public speak-
ing—Trier Social Stress Test) and in religious/spiritual contexts (Bible reading and
listening to sacred music) in 35 individuals with RSP and 35 matched participants.
We found no stress reduction in the religious/spiritual context in RSP, as indicated
by increased heart rate, saliva cortisol, and relatively higher left than right frontal
activity. Religious stimuli evoked physiological stress responses in RSP. Contrary
to the physiological parameters, participants with RSP reported less anxiety in the
religious/spiritual context. Religious individuals with and without RSP showed
similar stress responses during public speaking. Religious individuals without RSP
displayed reduced stress responses in the religious/spiritual context. These results
indicate that specific physiological distress in religious/spiritual contexts should be
considered in the psychological care of RSP.
* Szabolcs Kéri
[email protected]; [email protected]
1
Department of Cognitive Science, Budapest University of Technology and Economics, Egry J.
Str. 1, Budapest 1111, Hungary
2
National Institute of Mental Health, Neurology and Neurosurgery - Nyírő Gyula Hospital,
Budapest, Hungary
3
Faculty of Medicine, Department of Physiology, University of Szeged, Szeged, Hungary
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Introduction
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uncertainty, repetitive thought patterns, and rumination to cope with the stressful
situation effortfully (Düsing et al., 2016; Haehl et al., 2021; Roth & Cohen, 1986).
An essential and unexplored question is how individuals with RSP react in stress-
ful situations. To evaluate the specificity of stress reactivity, we compared two con-
ditions: exposition to challenging everyday situations (public speaking) and partici-
pating in religious/spiritual activities. For example, individuals with RSP may feel
overwhelmed when reading Bible verses relative to people with stable religiosity
who experience calming and supporting Bible reading. On the other hand, individu-
als with RSP may feel the same stress level as religious people without RSP during
mundane situations (e.g., social evaluation in public speaking).
Therefore, the hypotheses of the present study were the following:
Hypothesis 1 Individuals with and without RSP show similar anxiety, heart rate,
cortisol secretion, and lateralized frontal brain activity during the TSST.
Hypothesis 2 Individuals with RSP display increased anxiety, accelerated heart rate,
enhanced cortisol secretion, and higher left frontal activity than control participants
without RSP in a religious context (Bible reading and listening to sacred music).
We enrolled 35 individuals with RSP and 35 matched participants who did not
experience RSP from Hungary’s Roman Catholic, Protestant, and Pentecostal com-
munities. Participants with RSP attended the pastoral psychological care service
at the Nyírő Gyula Hospital (Budapest, Hungary). All of them defined themselves
as highly religious believers. People with RSP sought help because of questioning
their faith following adverse life events. They reported moral dilemmas concerning
work and political commitment, conflicts related to differences in religious views,
and feeling guilty because of prohibited sexual behavior. RSP resulted in existential
anxiety and interpersonal conflicts.
To evaluate possible psychiatric disorders and to define RSP, we used a struc-
tured clinical interview for DSM-5 (Diagnosis and Statistical Manual of Mental
Disorders—5) (First et al., 2016). The cultural impact on clinical presentation is
especially relevant in RSP. Therefore, we administered each participant the DSM-5
Cultural Formulation Interview (CFI) (American Psychiatric Association, 2013).
We did not include individuals with psychiatric disorders in the present study. How-
ever, all participants meet the DSM-5 definition of "Problems related to other psy-
chosocial, personal, and environmental circumstances" (Religious or Spiritual Prob-
lem, [RSP, code: V62.89] (American Psychiatric Association, 2013).
We also assessed general cognitive functioning [Wechsler Adult Intelligence
Scale-IV, WAIS-IV (Wechsler, 2008)], socioeconomic status [Hollingshead Four-
Factor Index of Socioeconomic Status, SES (Hollingshead, 1975)], subjective
depressive experiences [Beck Depression Inventory-II, BDI-II (Beck et al., 1996)],
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and anxiety [Beck Anxiety Inventory, BAI (Beck et al., 1988)] (Perczel-Forintos
et al., 2018; Rózsa et al., 2010).
To delineate the religious behavior of the participants, we administered the
modified Duke University Religiosity Index (DUREL), which assesses organized
religious activity, individual religious activity, and intrinsic religiosity (Koenig &
Büssing, 2010). During the recruitment of individuals with and without RSP, we
systematically screened for potential confounding factors in stress measurements,
including nicotine, caffeine, and alcohol intake, contraception use, body mass
index, chronic diseases (e.g., cardiovascular and metabolic diseases), and working
night shifts (Narvaez Linares et al., 2020). Table 1 depicts the characteristics of the
participants.
Main Assessment
Data are mean (standard deviation) except for gender distribution. The two groups were compared with
two-tailed t-tests
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recovery. During the baseline phase (30 min), we presented the essential informa-
tion and provided sufficient time to acclimatize. Next, at the end of the baseline
phase, we conducted the measurements (t[baseline]): visual analog scale (VAS) for
stress and anxiety, saliva cortisol, heart rate, and EEG. Immediately after this,
volunteers participated in the stress induction phase (20-min), which included the
TSST (simulated job interview and arithmetic calculations). At the end of the
stress induction phase, we repeated the measurements used at the end of the base-
line phase (t[stress]). Finally, we administered a recovery phase (40 min) when par-
ticipants relaxed and silently read verses from the Bible and listened to relaxing
religious piano music. Again, all measurements were repeated at the end of the
recovery phase ( t[recovery]).
Replication
We asked the participants to visit the laboratory approximately two weeks after
the main assessment. In this case, we performed the baseline and the recovery
phase of the original assessment (religious context) without social-evaluative
stress. The main question of the replication experiment was whether the religious
context (Bible reading and religious music) alone could elicit a stress response in
RSP. Thirty-one individuals with RSP and 32 matched participants without RSP
were willing to complete the replication phase from the original sample included
in the main assessment.
We used a public-speaking procedure based on the TSST, which has been shown
to evoke social-evaluative stress with increased cortisol secretion and EEG signa-
tures (Dickerson & Kemeny, 2004; Düsing et al., 2016). We considered the newest
available protocol for TSST, including a standardized background questionnaire for
confounding variables and physiological recordings (Narvaez Linares et al., 2020).
Participants were informed that the test measures their public speaking and cog-
nitive abilities in front of an expert committee. They performed a simulated job
interview and then arithmetic calculations (subtracting 13 from a random num-
ber > 4800) during the procedure. In the original version, volunteers spoke in front
of an audience, but in our study, participants performed in front of a video camera
(Düsing et al., 2016). The public-speaking phase was followed by a recovery period
(40-min), during which participants listened to the Hillsong worship piano (Mus-
selman, 2019) and silently read calming verses from the Bible (Zondervan, 2019).
The subjective experience of stress and anxiety was measured using a VAS (visual
analog scale comprising a horizontal line between 0 and 10 points on the computer
screen; 0—no stress and anxiety, 10—the highest stress level and anxiety). We
administered the VAS before the stress induction phase ( t[baseline]), immediately after
the stress induction phase ( t[stress]), and at the end of the recovery period (t[recovery]).
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EEG Measurements
We recorded resting-state EEG at three time points ( t[baseline], t[stress], t[recovery]). Each
measurement included eight 1-min resting periods (four occasions with eyes open
and four with eyes closed, counterbalanced across subjects). EEG was recorded and
processed with a NEUVO—CURRY 8X-system with a 256-channel Quik-Cap Neo
Net (high-density EEG cap, Ag/AgCl electrodes, four bipolar leads for vertical and
horizontal electrooculogram, extended international 10–20 system) (Compumedics,
NeuroScan). The electrode impedances were checked (< 5 kΩ, homologous bilat-
eral leads: < 1 kΩ). The sampling rate was 500 Hz. For data processing, we used
the EEGLAB interactive MATLAB toolbox (Schwartz Center for Computational
Neuroscience, University of California). Following built-in automatic and manual
artifact reduction, the 1-min epochs were segmented in 2-s periods with 75% overlap
between epochs (epoch amplitudes < ± 75 μV) and were low-pass filtered at 30 Hz
(Düsing et al., 2016). We used Fourier transformation to generate the spectral power
(μV2) (resolution of 0.488 Hz) in the alpha band (8–13 Hz). Every 1 min EEG reg-
istration included at least 20 2-s epochs, and power density was averaged using all
epochs. We used logarithmic transformation (ln) for averaged power density values.
We calculated the frontal asymmetry index for the 1-min epochs by subtracting the
logarithmically transformed alpha frequency of left electrode sites from homologous
right leads (e.g., F4-F3, F8-F7). Higher alpha-asymmetry scores indicate relatively
more robust left-sided frontal activation (Duan et al., 2019; Düsing et al., 2016).
Heart rate was measured with Frontier X chest-work heart monitor (Fourth Fron-
tier), which records a high-quality, continuous electrocardiogram (ECG) validated
against a GE Holter Monitor. We registered heart rates at three time points (t[baseline],
t[stress], t[recovery]). All data were processed offline. Two measurements were con-
ducted at each time point, and the average was analyzed.
Saliva samples were also collected from each participant at the same three time
points (t[baseline], t[stress], t[recovery]). We used SalivaBio Passive Drool Method for
saliva sample collection and stored the samples at − 10 °C. Free salivary corti-
sol concentrations were measured by using Salimetrics immunoassays (assay range:
0.012–3.00 µg/dL; sensitivity: < 0.007 µg/dL) (Szőllősi, Pajkossy, Demeter, Kéri, &
Racsmány, 2018). We analyzed two samples at each time point with excellent con-
sistency (< 2% differences between the two samples). The average of the two sam-
ples was used for data analysis.
Data Analysis
We used STATISTICA 13.5 (Tibco) for data analysis. Before considering para-
metric tests, all data were checked for normal distribution (Kolmogorov–Smirnov
test) and homogeneity of variance (Levene’s test). Repeated-measures analyses of
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Results
Anxiety‑VAS
Main Assessment
The ANOVA performed on the anxiety-VAS scores yielded significant main effects
of group (RSP vs. non-RSP) (F(1,68) = 8.71, p < 0.01, ƞ2 = 0.11) and test phase
(t[baseline], t[stress], and t[recovery]) (F(2,136) = 95.22, p < 0.001; ƞ2 = 0.25). The two-way
interaction between the group and test phase was not significant (p = 0.50). However,
Tukey’s HSD tests indicated no significant differences between individuals with and
without RSP at t[baseline], t[stress], and t[recovery]) (ps > 0.2). Both groups scored higher
in the stress phase than in the baseline phase ( t[stress] > t[baseline]), and the anxiety-VAS
scores declined in the recovery phase (t[recovery] < t[stress]) (ps < 0.05) (Fig. 1A).
Replication
There were significant main effects of group (F(1,61) = 6.30, p < 0.05, ƞ2 = 0.09)
(RSP vs. non-RSP) and test phase (baseline, religious context) (F(1,61) = 17.16,
p < 0.001; ƞ2 = 0.22). The two-way interaction between the group and test phase
was not significant (p = 0.80). Tukey’s HSD tests revealed no significant differences
between RSP and non-RSP participants. In both groups, we observed a reduction of
anxiety-VAS scores during the religious context phase (ps < 0.05) (Fig. 2A).
EEG Measures
Main Assessment
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Fig. 1 Behavioral and physiological measures in individuals with Religious or Spiritual Problem (RSP)
and matched religious individuals without RSP (non-RSP). The stress phase included a public speech
(social-evaluative stress). During the recovery phase, participants read calming Bible verses and listened
to sacred music. Data are mean, and error bars indicate 95% confidence intervals. * p < .001, RSP vs.
non-RSP, Tukey’s HSD tests
Fig. 2 Behavioral and physiological measures from the replication assessment in individuals with Reli-
gious or Spiritual Problem (RSP) and matched religious individuals without RSP (non-RSP). The reli-
gious context included reading calming Bible verses and listening to sacred music. Data are mean, and
error bars indicate 95% confidence intervals. *p < .001, RSP vs. non-RSP, Tukey’s HSD tests
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(F(2,136) = 8.24, p < 0.001, ƞ2 = 0.11). The two-way interaction was also signifi-
cant (F(2,136) = 23.91, p < 0.001, ƞ2 = 0.26). There were no significant differences
between the RSP and non-RSP groups in the baseline and stress phases (t[baseline]
and t[stress], ps > 0.05). However, individuals with RSP displayed significantly
higher frontal asymmetry in the recovery phase relative to the non-RSP participants
(t[recovery], p < 0.001). It is noteworthy that in the RSP group, the frontal asymme-
try values significantly increased in the recovery phase relative to the stress phase
(t[recovery] > t[stress]; p < 0.001). In the non-RSP group, we found the opposite effect:
the frontal asymmetry index was lower in the recovery phase than in the stress phase
(t[recovery] < t[stress], p < 0.05) (Fig. 1B).
Replication
We again found significant main effects of group (F(1,61) = 26.15, p < 0.001,
ƞ2 = 0.30) and test phase (baseline vs. religious context) (F(1,61) = 10.10, p < 0.001,
ƞ2 = 0.14). The two-way interaction was also significant (F(1,61) = 29.83, p < 0.001,
ƞ2 = 0.33). At baseline, there were no significant differences between RSP and non-
RSP participants (p = 0.9), but in the religious context, individuals with RSP display
markedly higher frontal asymmetry index (p < 0.001) (Fig. 2B).
Main Assessment
The ANOVA investigating heart rate indicated significant main effects of group
(F(1,68) = 14.12, p < 0.001, ƞ2 = 0.17) and test phase (F(2,136) = 45.21, p < 0.001,
ƞ2 = 0.40). The two-way interaction was significant (F(2,136) = 20.78, p < 0.001,
ƞ2 = 0.23). We found no significant differences between the RSP and non-RSP
groups in the baseline and stress phases (t[baseline] and t[stress], ps > 0.05). However,
individuals with RSP displayed significantly higher heart rate in the recovery phase
relative to the non-RSP participants (t[recovery], p < 0.001). In the RSP group, heart
rate did not change in the recovery phase compared to the stress phase (t[stress] =
t[recovery], p > 0.5). In the non-RSP group, heart rate returned to the baseline level in
the recovery phase (t[recovery] = t[baseline] < t[stress,], p < 0.001) (Fig. 1C).
The ANOVA performed on saliva cortisol indicated significant main effects of
group (F(1,68) = 12.23, p < 0.001, ƞ2 = 0.15), test phase (F(2,136) = 6.98, p < 0.01,
ƞ2 = 0.09), and an interaction between group and test phase (F(2,136) = 9.32,
p < 0.001, ƞ2 = 0.12). Similar to the heart rate, individuals with and without RSP
differed only in the recovery phase when RSP individuals showed elevated saliva
cortisol levels (p < 0.001). Significant decreases in saliva cortisol levels were only
seen in participants without RSP ( t[recovery] < t[stress], p < 0.05). In the RSP group, we
observed paradoxically higher saliva cortisol concentrations in the recovery phase
compared to the stress phase (t[recovery] > t[stress], p < 0.05) (Fig. 1D).
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Replication
In the case of heart rate, there was a significant main effect of group (RSP vs. non-
RSP) (F(1,61) = 38.50, p < 0.001, ƞ2 = 0.39), and a significant interaction between
group and task phase (baseline vs. religious context) (F(1,62) = 28.95, p < 0.001,
ƞ2 = 0.32). At baseline, we measured similar heart rate in RSP and non-RSP partici-
pants (p = 0.90). In the religious context, individuals with RSP displayed increased
heart rate. In contrast, participants without RSP showed decreased heart rate
(ps < 0.05) (Fig. 2C).
In the case of saliva cortisol, we found significant main effects of group (RSP
vs. non-RSP) (F(1,61) = 9.29, p < 0.01, ƞ2 = 0.13), task phase (baseline vs. religious
context) (F(1,61) = 5.45, p < 0.05, ƞ2 = 0.08), and a two-way interaction between
them (F(1,61) = 32.94, p < 0.001, ƞ2 = 0.35). The post hoc tests indicated that
individuals with RSP showed increased cortisol secretion in the religious context
(p < 0.001). In contrast, non-RSP participants did not display a similar change in
cortisol secretion (p = 0.08, a tendency of decreased cortisol secretion in the reli-
gious context) (Fig. 2D).
Discussion
The core finding of the present study was that individuals with RSP exhibited
increased stress responses only in a religious context relative to matched religious
people without RSP. We also found that during social-evaluative stress, the RSP and
non-RSP groups showed similar responses on subjective anxiety ratings, physiologi-
cal measures (cardiovascular activity and cortisol secretion), and lateralized frontal
EEG activity. Moreover, when the social-evaluative stress situation was followed by
a recovery phase in a religious context (Bible reading and sacred music), only peo-
ple without RSP displayed alleviated stress responses. It is essential to underline that
the results were replicated when the task was solely Bible reading and listening to
sacred music without preceding social-evaluative stress, confirming that religious
materials alone can be stressful at the physiological level in people with RSP.
The results from the present study are in accordance with the findings of Stauner
et al. (2016). In this study, the authors identified a general factor in addition to the
five components of religious/spiritual struggle (divine, demonic, interpersonal,
moral, and doubt-related). The general factor showed a definitive correlation with
religiousness but did not alter the correlation of the five factors with neuroticism,
depression, anxiety, and stress (Stauner et al., 2016). The findings of Stauner et al.
(2016) confirmed that religious/spiritual struggle is a psychological construct differ-
ent from religiosity and stress.
Multiple factors contribute to the emergence of religious/spiritual struggle,
including the negative appraisal of stressful situations, negative affectivity, and inse-
cure and ambivalent attachment to God (Ano & Pargament, 2013). When adverse
life events are appraised as a sacred loss, individuals experience intrusive thoughts,
depression, and pronounced posttraumatic growth (appreciation of life, deepened
relationships with others, spiritual change, new possibilities, and empowerment)
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Limitations
There are several limitations to consider during the interpretation of our results.
First, as mentioned above, religious coping strategies were not assessed. Second,
the sample was confined to a relatively small number of help-seeking individuals.
To improve statistical power and to perform correlational and mediation analyses
among behavioral parameters, physiological measures, and brain activity, we need
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larger representative samples in which scales for religious coping and struggle are
administered. Third, we need long-term data on the mental and physical health of
the participants, which warrants future studies to focus on the direct relationship
between RSP, physiological changes, health status, and well-being. Fourth, to avoid
type 2 errors, we strictly reduced the variables according to the main hypotheses.
For example, only heart rate indexed cardiovascular reactivity, and we did not meas-
ure pro-inflammatory cytokines during the stress response.
Conclusions
Funding Open access funding provided by Budapest University of Technology and Economics. The
authors have not disclosed any funding.
Declarations
Conflict of interest The author declares no commercial or financial conflict of interest.
Informed Consent All participants gave written informed consent and were informed that they could with-
draw from the study at any time.
Ethical Approval The study was carried out following the Declaration of Helsinki and respective ethical
standards at the National Institute of Mental Health, Neurology and Neurosurgery—Nyírő Gyula Hospital,
Budapest, Hungary. The National Medical Research Council approved the study.
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License,
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you give appropriate credit to the original author(s) and the source, provide a link to the Creative Com-
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directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licen
ses/by/4.0/.
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References
Ai, A. L., Pargament, K. I., Appel, H. B., & Kronfol, Z. (2010b). Depression following open-heart sur-
gery: A path model involving interleukin-6, spiritual struggle, and hope under preoperative distress.
Journal of Clinical Psychology, 66(10), 1057–1075. https://doi.org/10.1002/jclp.20716
Ai, A. L., Pargament, K., Kronfol, Z., Tice, T. N., & Appel, H. (2010a). Pathways to postoperative hostil-
ity in cardiac patients: Mediation of coping, spiritual struggle and interleukin-6. Journal of Health
Psychology, 15(2), 186–195. https://doi.org/10.1177/1359105309345556
Allen, J. J., & Cohen, M. X. (2010). Deconstructing the “resting” state: Exploring the temporal dynamics
of frontal alpha asymmetry as an endophenotype for depression. Frontiers in Human Neuroscience,
4, 232. https://doi.org/10.3389/fnhum.2010.00232
American Psychiatric Association. (2013). Diagnostic and Statistical Manual of Mental Disorders (DSM-
5). American Psychiatric Press.
American Psychiatric Association. (2022). Diagnostic and statistical manual of mental disorders. Ameri-
can Psychiatric Press.
Ano, G. G., & Pargament, K. I. (2013). Predictors of spiritual struggles: An exploratory study. Mental
Health, Religion & Culture, 16, 419–434. https://doi.org/10.1080/13674676.2012.680434
Ano, G. G., & Vasconcelles, E. B. (2005). Religious coping and psychological adjustment to stress: A
meta-analysis. Journal of Clinical Psychology, 61(4), 461–480. https://doi.org/10.1002/jclp.20049
Bali, A., & Jaggi, A. S. (2015). Clinical experimental stress studies: Methods and assessment. Reviews in
the Neurosciences, 26(5), 555–579. https://doi.org/10.1515/revneuro-2015-0004
Beck, A. T., Epstein, N., Brown, G., & Steer, R. A. (1988). An inventory for measuring clinical anxiety:
Psychometric properties. Journal of Consultant and Clinical Psychology, 56(6), 893–897.
Beck, A. T., Steer, R. A., Ball, R., & Ranieri, W. (1996). Comparison of beck depression inventories - IA
and -II in psychiatric outpatients. Journal of Personality Assessment, 67(3), 588–597. https://doi.
org/10.1207/s15327752jpa6703_13
Carter, W. R., Johnson, M. C., & Borkovec, T. D. (1986). Worry: an electrocortical analysis. Advances
in Behaviour Research and Therapy, 8(4), 193–204. https://doi.org/10.1016/0146-6402(86)90004-4
Cheng, C., & Ying, W. (2023). A meta-analytic review of the associations between dimensions of reli-
gious coping and psychological symptoms during the first wave of the COVID-19 pandemic. Fron-
tiers in Psychiatry, 14, 1097598. https://doi.org/10.3389/fpsyt.2023.1097598
Coan, J. A., & Allen, J. J. (2004). Frontal EEG asymmetry as a moderator and mediator of emotion. Bio-
logical Psychology, 67(1–2), 7–49. https://doi.org/10.1016/j.biopsycho.2004.03.002
Davidson, R. J. (2004). What does the prefrontal cortex “do” in affect: Perspectives on frontal EEG asym-
metry research. Biological Psychology, 67(1–2), 219–233. https://doi.org/10.1016/j.biopsycho.2004.
03.008
Dickerson, S. S., & Kemeny, M. E. (2004). Acute stressors and cortisol responses: A theoretical integra-
tion and synthesis of laboratory research. Psychological Bulletin, 130(3), 355–391. https://doi.org/
10.1037/0033-2909.130.3.355
Duan, H., Fang, H., Zhang, Y., Shi, X., & Zhang, L. (2019). Associations between cortisol awakening
response and resting electroencephalograph asymmetry. PeerJ, 7, e7059. https://doi.org/10.7717/
peerj.7059
Düsing, R., Tops, M., Radtke, E. L., Kuhl, J., & Quirin, M. (2016). Relative frontal brain asymmetry and
cortisol release after social stress: The role of action orientation. Biological Psychology, 115, 86–93.
https://doi.org/10.1016/j.biopsycho.2016.01.012
Engels, A. S., Heller, W., Mohanty, A., Herrington, J. D., Banich, M. T., Webb, A. G., & Miller, G. A.
(2007). Specificity of regional brain activity in anxiety types during emotion processing. Psycho-
physiology, 44(3), 352–363. https://doi.org/10.1111/j.1469-8986.2007.00518.x
Exline, J. J., Pargament, K. I., Grubbs, J. B., & Yali, A. M. (2014). The Religious and Spiritual Strug-
gles Scale: Development and initial validation. Psychology of Religion and Spirituality, 6, 208–222.
https://doi.org/10.1037/a0036465
Exline, J. J., & Rose, E. (2005). Religious and spiritual struggles. In R. F. Paloutzian & C. L. Park (Eds.),
Handbook of the Psychology of Religion and Spirituality (pp. 315–330). Guilford.
First, M. B., Williams, J. B. W., Karg, R. S., & Spitzer, R. L. (2016). Structured Clinical Interview for
DSM-5 Disorders—Clinician Version (SCID-5-CV). American Psychiatric Association Publishing.
Greenfield, E. A., & Marks, N. F. (2007). Religious social identity as an explanatory factor for asso-
ciations between more frequent formal religious participation and psychological well-being.
13
Journal of Religion and Health
13
Journal of Religion and Health
Perczel-Forintos, D., Ajtay, G., Barna, C., Kiss, Z., & Komlósi, S. (2018). Kérdőívek, becslőskálás a
klinikai pszichológiában. Medicina.
Pitchford, B., & Arnell, K. M. (2019). Self-control and its influence on global/local processing: An inves-
tigation of the role of frontal alpha asymmetry and dispositional approach tendencies. Attention,
Perception, & Psychophysics, 81(1), 173–187. https://doi.org/10.3758/s13414-018-1610-z
Pomerleau, J. M., Pargament, K. I., Krause, N., Ironson, G., & Hill, P. (2020). Religious and spiritual
struggles as a mediator of the link between stressful life events and psychological adjustment in
a nationwide sample. Psychology of Religion and Spirituality, 12(4), 451–459. https://doi.org/10.
1037/rel0000268
Prusak, J. (2016). Differential diagnosis of Religious or Spiritual Problem possibilities and limitations
implied by the V-code 6289 in DSM-5. Psychiatria Polska, 50(1), 175–186.
Ramirez, S. P., Macêdo, D. S., Sales, P. M., Figueiredo, S. M., Daher, E. F., Araújo, S. M., Pargament,
K. I., Hyphantis, T. N., & Carvalho, A. F. (2012). The relationship between religious coping, psy-
chological distress and quality of life in hemodialysis patients. Journal of Psychosomatic Research,
72(2), 129–135. https://doi.org/10.1016/j.jpsychores.2011.11.012
Reznik, S. J., & Allen, J. J. B. (2018). Frontal asymmetry as a mediator and moderator of emotion: an
updated review. Psychophysiology. https://doi.org/10.1111/psyp.12965
Roth, S., & Cohen, L. J. (1986). Approach, avoidance, and coping with stress. American Psychologist,
41(7), 813–819. https://doi.org/10.1037//0003-066x.41.7.813
Rózsa, S., Kő, N., Mészáros, A., Kuncz, E., & Mlinkó, R. (2010). Wechsler Felnőtt Intelligenciateszt -
negyedik kiadás. OS Hungary.
Sapolsky, R. M. (2021). Glucocorticoids, the evolution of the stress-response, and the primate predica-
ment. Neurobiology of Stress, 14, 100320. https://doi.org/10.1016/j.ynstr.2021.100320
Schnell, T., Fuchs, D., & Hefti, R. (2020). Worldview under stress: Preliminary findings on cardiovascular
and cortisol stress responses predicted by secularity, religiosity, spirituality, and existential search.
Journal of Religion and Health, 59(6), 2969–2989. https://doi.org/10.1007/s10943-020-01008-5
Schwalm, F. D., Zandavalli, R. B., de Castro Filho, E. D., & Lucchetti, G. (2022). Is there a relation-
ship between spirituality/religiosity and resilience? A systematic review and meta-analysis of obser-
vational studies. Journal of Health Psychology, 27(5), 1218–1232. https://doi.org/10.1177/13591
05320984537
Sephton, S. E., Koopman, C., Schaal, M., Thoresen, C., & Spiegel, D. (2001). Spiritual expression and
immune status in women with metastatic breast cancer: An exploratory study. Breast Journal, 7(5),
345–353. https://doi.org/10.1046/j.1524-4741.2001.20014.x
Stauner, N., Exline, J. J., Grubbs, J. B., Pargament, K. I., Bradley, D. F., & Uzdavines, A. (2016). Bifactor
models of religious and spiritual struggles: distinct from religiousness and distress. Religions, 7(6),
68.
Tobin, E. T., & Slatcher, R. B. (2016). Religious participation predicts diurnal cortisol profiles 10 years
later via lower levels of religious struggle. Health Psychology, 35(12), 1356–1363. https://doi.org/
10.1037/hea0000372
Tops, M., Quirin, M., Boksem, M. A. S., & Koole, S. L. (2017). Large-scale neural networks and the
lateralization of motivation and emotion. International Journal of Psychophysiology, 119, 41–49.
https://doi.org/10.1016/j.ijpsycho.2017.02.004
Urry, H. L., Nitschke, J. B., Dolski, I., Jackson, D. C., Dalton, K. M., Mueller, C. J., Rosenkranz, M. A.,
Ryff, C. D., Singer, B. H., & Davidson, R. J. (2004). Making a life worth living: Neural correlates
of well-being. Psychological Science, 15(6), 367–372. https://doi.org/10.1111/j.0956-7976.2004.
00686.x
Wechsler, D. (2008). Wechsler adult intelligence scale (4th ed.). Pearson.
Zhang, X., Bachmann, P., Schilling, T. M., Naumann, E., Schachinger, H., & Larra, M. F. (2018). Emo-
tional stress regulation: The role of relative frontal alpha asymmetry in shaping the stress response.
Biological Psychology, 138, 231–239. https://doi.org/10.1016/j.biopsycho.2018.08.007
Zondervan. (2019). The God of comfort: 100 Bible verses to soothe our spirit. Zondervan
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