Study Results
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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COMPLETED
NA
80 participants
INTERVENTIONAL
2025-01-25
2025-04-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
SUPPORTIVE_CARE
TRIPLE
Study Groups
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Progressive relaxation group
Progressive Relaxation Exercises
Progressive Relaxation Exercise
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.
No interventions assigned to this group
Interventions
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Progressive Relaxation Exercise
Progressive Relaxation Exercise Steps
Eligibility Criteria
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Inclusion Criteria
* 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
* 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
18 Years
30 Years
ALL
Yes
Sponsors
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Kutahya Health Sciences University
OTHER
Responsible Party
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Necibe Dağcan
Assistant Professor of Nursing
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)
Countries
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Other Identifiers
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KutahyaHSU-NECİBE-DAĞCAN-0004
Identifier Type: -
Identifier Source: org_study_id
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