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DepressionPRMNURSENCT07038109

Progressive Muscle Relaxation in Nursing Students: Effects on Psychological and Biopsychosocial Outcomes

A study testing Progressive relaxation exercise in people with Depression and Anxiety, run by Ondokuz Mayıs University at 1 site in Turkey (Türkiye).

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record

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Trial summary

This randomised controlled trial aims to investigate the effects of progressive muscle relaxation exercises (PMRE) on depression, anxiety, stress, future-oriented attitudes, and biopsychosocial responses in nursing students. Read more about this study

Who is it for?
Any ageHealthy volunteers can take part
Conditions the study is for
Depression, Anxiety, Stress, Psychological
What is being tested?
Progressive relaxation exercise
Could I receive a placebo?
No, everyone receives an active treatment
How many people
104 participants
Where
1 siteTurkey (Türkiye)
Study dates
1 Jan 2025to 1 Mar 2025
Phase
Interventional

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages Any age
  • All sexes
  • Healthy volunteers accepted
  • Child, Adult, Older adult

Who may be able to join

  • Being registered in the Department of Nursing
  • Voluntary consent to participate in the study

Who cannot join

  • Having joint or muscle pain, or any condition that may interfere with performing relaxation exercises
  • Having a diagnosis of cancer or any chronic disease
  • Having a psychiatric disorder that may interfere with obtaining valid results from the study (e.g., major depressive disorder, severe anxiety disorders, serious psychiatric conditions)
  • Currently receiving antidepressant, anxiolytic, or similar psychiatric treatment
  • Regular use of non-pharmacological methods such as yoga, psychotherapy, or similar practices

Trial locations and contacts

1 site in 1 country.

Turkey (Türkiye)1 site
  • Ondokuz Mayıs University

    Samsun

Other trials in Turkey (Türkiye)

About this study

Official title: Effects of Progressive Muscle Relaxation on Depression, Anxiety, Stress, Future Attitudes, and Biopsychosocial Responses in Nursing Students: A Randomized Controlled Trial

This randomised controlled trial aims to investigate the effects of progressive muscle relaxation exercises (PMRE) on depression, anxiety, stress, future-oriented attitudes, and biopsychosocial responses in nursing students. The study was conducted between June 2024 and June 2025 with students enrolled in the Nursing Department. Data collection took place between January and March 2025. When selecting participants, a list of participants meeting the inclusion criteria was created using snowball sampling. A total of 104 students were randomly divided into experimental and control groups of 52 students each. Data were collected using the DASS-21, Future Orientation Scale, and Biopsychosocial Response Scale for Nursing Students.

Read the detailed description

Nursing students often face academic stress, emotional demands and clinical responsibilities, which can lead to psychological problems such as depression, anxiety, stress and concerns about their future. These issues can affect both their well-being and professional competence. Progressive muscle relaxation exercises (PMRE) are recognised as a useful method for reducing muscle tension, managing stress, and improving emotional regulation.

This randomised controlled trial was conducted between June 2024 and June 2025 with students studying Nursing. The data collection phase was carried out between January and March 2025. Participants meeting the inclusion criteria were identified using snowball sampling, and a list was created. A total of 104 nursing students on this list were randomly assigned to either an experimental group (receiving PMRE) or a control group, with 52 participants in each group. A pre-test-post-test design was used. Measurement tools included the Depression, Anxiety and Stress Scale (DASS-21), the Future Orientation Scale, and the Biopsychosocial Response Scale for Nursing Students.

This study was supported by the Turkish Scientific and Technological Research Council (TÜBİTAK) under the 2209-A University Student Research Projects Support Programme.

Being tested
Progressive relaxation exercise
Keywords
Progressive Muscle Relaxation, Psychological Intervention, Nursing Students, Mental Health Promotion, Stress Management, Depression, Anxiety, Psychological Stress, Biopsychosocial Response, Future Orientation, University Students, Randomized Controlled Trial, Relaxation Techniques, progressive relaxation exercise
Medical subject headings
Depression, Anxiety Disorders, Stress, Psychological, Psychological Well-Being, Psychophysiologic Disorders

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Progressive relaxation exerciseOther

    Also called progressive muscle relaxation, progressive muscle relaxation exercises, Progressive Relaxation Technique, Jacobson's Progressive Muscle Relaxation

    The intervention was based on Jacobson's Progressive Muscle Relaxation (PMR) technique. Participants in the experimental group practiced PMR three times per week for four weeks. Each session lasted approximately 45 minutes and was conducted in a quiet environment. In the first session, the researcher provided face-to-face instruction. Subsequent sessions were guided by standardized audio recordings, and the participants were followed through scheduled online video calls. The intervention aimed to reduce depression, anxiety, and stress symptoms and to promote biopsychosocial well-being in nursing students.

Study groups in NCT07038109
Study groupRoleWhat they receive
Participants in this group received progressive relaxation exercises (PRE)ExperimentalA structured progressive muscle relaxation program based on Jacobson's technique was implemented. The intervention lasted four weeks, with participants practicing three times per week in 45-minute sessions. The exercises were initially demonstrated in person by the researcher to ensure correct technique. Subsequently, participants followed pre-recorded audio instructions during each session to maintain consistency. The intervention aimed to reduce psychological symptoms and support biopsychosocial well-being in nursing students.
Receives: Other: Progressive relaxation exercise
Control groupNo interventionParticipants in this group did not receive any behavioral or psychological intervention during the study period. They continued their normal academic activities without any additional support or guidance. No relaxation techniques or recordings were provided to this group. Data were collected at the same time points as the experimental group to ensure consistency in measurement.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Change in depression, anxiety, and stress levels measured by DASS-21

    The Depression Anxiety Stress Scale - 21 (DASS-21) will be used to assess changes in psychological symptoms. It consists of three subscales measuring depression, anxiety, and stress. The scale will be administered at baseline (pre-test) and after the 4-week intervention (post-test).

    Measured: Baseline and Week 4

Secondary outcomes (2)
  1. Change in future orientation levels measured by the Future Orientation Scale

    The Future Orientation Scale will be used to evaluate students' attitudes toward the future, including goal-setting, planning, and optimism. The scale will be administered before and after the intervention to detect changes.

    Measured: Baseline and Week 4

  2. Change in biopsychosocial response levels measured by the Biopsychosocial Response Scale for Nursing Students

    This scale measures students' emotional, physical, and social stress-related symptoms. It will be administered at baseline and after the intervention to assess changes in biopsychosocial well-being.

    Measured: Baseline and Week 4

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted26 Jun 2025
  2. Study start1 Jan 2025
  3. Primary completion1 Mar 2025
  4. Study completion1 Mar 2025

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Supportive care
Allocation
Randomised
Intervention model
Parallel groups
Model description
This study used a two-arm, parallel assignment design. Participants were randomly assigned to either the experimental group, which received progressive muscle relaxation exercises, or the control group, which received no intervention. A pretest-posttest design was used to assess outcomes.
Masking
Double blind
Who is masked
Participant, Outcomes assessor
Enrolment
104 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07038109
Sponsor's protocol ID
HEM-PGE-RCT-2024-TUBITAK2209-A
Other IDs
1919B012327345
Acronym
PRMNURSE
Status last verified
Mar 2026
First submitted
18 Jun 2025
Last updated
12 Mar 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: Individual participant data (IPD) will not be shared due to ethical restrictions and the scope of the study. The research was conducted as part of a TÜBİTAK 2209-A student project and approved only for academic use. No explicit consent or ethical approval was obtained for external data sharing.

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