Effects of Progressive Relaxation Exercises

NCT ID: NCT06867575

Last Updated: 2025-08-29

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

80 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-01-25

Study Completion Date

2025-04-30

Brief Summary

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When the literature is examined, it is observed that the effects of progressive relaxation exercises on pain, anxiety and sleep quality have been frequently investigated in different populations. Studies conducted with nursing students focus on dysmonorrhea and clinical anxiety and stress . A limited number of studies have focused on the quality of life of students . There is no study examining the effects of progressive relaxation exercises on sleep quality, psychological endurance and quality of life together. Therefore, the aim of our study is to examine the effects of progressive relaxation exercises applied to nursing students on sleep quality, psychological endurance and quality of life. It is thought that our study results will contribute to the literature in terms of their originality.

Detailed Description

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This research is a randomized controlled trial planned to examine the effects of progressive relaxation exercises on sleep quality, psychological resilience and quality of life in nursing students.

Conditions

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Nursing Caries Progression Sleep

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

This research is a randomized controlled trial planned to examine the effects of progressive relaxation exercises on sleep quality, psychological resilience and quality of life in nursing students.
Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

TRIPLE

Participants Investigators Outcome Assessors
Students will be randomly assigned (using online randomization software) to experimental and control groups. Students will know that they are participating in the study and the interventions that will be applied to them, but they will be blinded by not knowing which group they are in. The study data will be collected by a second researcher who is blinded to the groups. In the statistical analysis of the data, the groups will be labeled as group 1 and group 2, and the third researcher will be blinded when evaluating the results. Thus, the third researcher will be blinded to the study groups. In order to avoid bias in the evaluation of the results, the first researcher, who is not blinded, will not participate in any stage of the evaluation process.

Study Groups

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Progressive relaxation group

Progressive Relaxation Exercises

Group Type EXPERIMENTAL

Progressive Relaxation Exercise

Intervention Type OTHER

Progressive Relaxation Exercise Steps

Control group

The students who formed the control group and accepted to participate in the study will be asked to fill out the "Descriptive Characteristics Form", "Pittsburgh Sleep Quality Index (PSQI)", "Adult Resilience Scale", and "SF-36 Quality of Life Scale" in the first meeting. After filling out the data collection tools in the first meeting in the classroom, no intervention will be made. At the end of the 4th week follow-up period, separate data collection forms and post-test results will be obtained. The control group will be given a progressive relaxation exercise audio recording and booklets with written instructions stated in the audio recording.

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Progressive Relaxation Exercise

Progressive Relaxation Exercise Steps

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Being a student in the Department of Nursing

* Being willing to participate in the study
* Not having a chronic disease that may prevent exercise (COPD, heart failure, etc.)
* Not having a hearing problem
* Not having a psychiatric diagnosis (major depression, anxiety disorders, etc.) and not using medication for anxiety or depression
* Having a computer and technological devices at home
* Being able to use a mobile phone (IOS-Android)
* Having internet access
* Being able to speak Turkish
* Not having used techniques such as meditation, hypnosis, yoga for the last 6 months before the study
* Not having a neurological, systemic, or psychiatric disease.

Exclusion Criteria

* • Nursing students who do not volunteer to participate in the study,

* Those who have any health problems during the application process,
* Those who cannot continue the study for any reason,
* Those who want to withdraw from the study with their own consent
Minimum Eligible Age

18 Years

Maximum Eligible Age

30 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Kutahya Health Sciences University

OTHER

Sponsor Role lead

Responsible Party

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Necibe Dağcan

Assistant Professor of Nursing

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Necibe DAĞCAN ŞAHİN, PhD

Role: PRINCIPAL_INVESTIGATOR

Kütahya Health Sciences University, Faculty of Health Sciences

Burcu NAL, PhD

Role: STUDY_DIRECTOR

Kütahya Health Sciences University, Faculty of Health Sciences

Sema ÜSTÜNDAĞ, PhD (c)

Role: STUDY_DIRECTOR

Kütahya Health Sciences University, Faculty of Health Sciences

Locations

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Necibe

Kütahya, , Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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KutahyaHSU-NECİBE-DAĞCAN-0004

Identifier Type: -

Identifier Source: org_study_id

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