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Stress Reduction Program for Iraqi Medical Students

Effects of Stress Reduction Intervention on Psychological, Cardiovascular, and Neuroendocrine Outcomes in Iraqi Medical Students During Examinations

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07451145
Acronym
SRIMS
Enrollment
135
Registered
2026-03-05
Start date
2024-10-01
Completion date
2025-01-01
Last updated
2026-03-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Psychological Stress, Academic Stress

Keywords

ACTH, Cortisol, DHEA, HPA axis, Stress reduction, Stress management, Mindfulness, Medical students, Academic stress, Psychological stress, Neuroendocrine, Iraq, Examination stress, Behavioral intervention, Stress hormones

Brief summary

A 4-week stress reduction program for medical students during exams, measuring effects on stress, heart rate, blood pressure, and stress hormones (ACTH, cortisol, DHEA).

Detailed description

This single-group pre-post intervention study evaluates the effects of a culturally adapted 4-week stress-reduction program on psychological well-being, cardiovascular function, and hypothalamic-pituitary-adrenal (HPA) axis hormones in Iraqi medical students during examinations. A total of 135 medical students participated in an 8-session mindfulness-based stress management program. Primary outcomes included perceived stress (0-10 visual analog scale), heart rate, blood pressure, and serum levels of ACTH, cortisol, and DHEA, measured before and after the intervention.

Interventions

Culturally adapted 4-week stress reduction program including: * 8 group sessions (2 per week, 90 minutes each) * Mindfulness meditation techniques * Progressive muscle relaxation * Breathing exercises * Psychoeducation about stress * Daily home practice (15-20 minutes) * Led by trained facilitators

Sponsors

University of Thi-Qar
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

Single-group pre-post intervention study. All 135 participants received an identical 8-session mindfulness-based stress reduction program delivered over 4 weeks. Outcome measures (stress, ACTH, cortisol, DHEA, heart rate, blood pressure) were assessed at baseline before the intervention and again at 4 weeks after program completion.

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* \- Medical students at University of Thi-Qar College of Medicine * Currently enrolled and preparing for examinations * Age 18 years or older * Willing to participate in 8 intervention sessions * Able to provide informed consent

Exclusion criteria

* Current use of medications affecting HPA axis or cardiovascular function * Diagnosed chronic medical or psychiatric conditions * Pregnancy or lactation * Previous participation in formal mindfulness or stress management training

Design outcomes

Primary

MeasureTime frameDescription
Perceived Stress ScoreBaseline and 4 weeksPerceived Stress Score (0-10 visual analog scale)
ACTH LevelsBaseline and 4 weeksMeasure: Levels (pg/mL)
Cortisol LevelsBaseline and 4 weeksMeasure: Cortisol Levels (µg/dL)
DHEA LevelsBaseline and 4 weeksMeasure: DHEA Levels (ng/mL)

Secondary

MeasureTime frameDescription
Heart RateBaseline and 4 weeksMeasure: Heart Rate (bpm)
Blood PressureBaseline and 4 weeksMeasure: Blood Pressure (mmHg) - Systolic and Diastolic

Countries

Iraq

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 6, 2026