- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06079463
The Effect of Progressive Relaxation Exercise on Anxiety and Quality of Life of Diabetic Patients
Determining the Effect of Progressive Relaxation Exercise on Anxiety and Quality of Life in Diabetes Patients
Purpose of the study: The study aimed to direct the anxiety and quality of life of progressive movement exercise in diabetic patients.
Type of research: A randomized controlled pre-test-post-test study was planned with the aim of directing progressive movement exercise on anxiety and quality of life in diabetics.
research questions Q1: Does progressive movement exercise have an effect on diabetic anxiety and quality of life? Population of the Research and Sample Selection: The home of the research will be the diabetes windows to the internal service on data collection. G-power 3.1 analysis program environment to calculate large sample size. Sampling of the research; With 0.61% effect sizes, 0.05% error level, 95% confidence interval and 80% power to show the universe, 52 people took part in the experimental motivations (phased training exercises group) and 52 people took part in the control slots, for a total of 104 people. Sample selection criteria patients are randomized using the Random Integer Generator method from the Numbers subheading on the Random.org website. In randomization, aspects will be collected representatively of 1 experimental group and 2 control groups.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Gazi Baran CAMCİ
- Phone Number: 5059779139
- Email: baran.cmmci@outlook.com
Study Contact Backup
- Name: Esin Kavuran
- Phone Number: 5374302319
Study Locations
-
-
-
Erzurum, Turkey, 25030
- Recruiting
- Atatürk Üniversitesi
-
Contact:
- Esin Kavuran, Phd
- Phone Number: 5374302319
- Email: esinkavuran@hotmail.com
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Diabetic patients who will be treated in the Internal Medicine Service who want to participate in the study voluntarily.
- Patients over the age of 18
Exclusion Criteria:
- Patients who do not want to participate in the study.
- Patients who are unable to perform the progressive relaxation exercise (amputation, etc.).
- Pregnant or breastfeeding patients
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Diabetic patients undergoing progressive relaxation exercise
After the purpose of the study was explained and their verbal and written consents were obtained, a questionnaire including the Beck Anxiety Scale, which includes the socio-demographic characteristics, and the World Health Organization Quality of Life Scale, were applied to the patients in the experimental and control groups.
will participate in the research, will be asked, and will be filled in face to face by the responsible researcher.
After the progressive relaxation exercise training is given to the experimental group patients, the voice recording containing the commands for the application of the progressive relaxation exercise will be sent to the phone of the patient and/or their relatives.
Patients in the experimental group spent an average of 25-30 minutes each day for four weeks.
Ongoing exercises will be conducted and followed up.
At the end of the fourth week, "Beck Anxiety Scale and World Health Organization Quality of Life Scale" will be applied.
|
Step 1: Take a comfortable position (sitting or lying down) and wear comfortable, non-tightening clothes. Step 2: Try to relax with eyes closed, without focusing on thoughts, by focusing on your own body muscles. Step 3: Right and left, respectively, hands, arms (triceps muscle), chest, abdomen, hips, legs (thigh muscles), feet and toes, neck, shoulder (scapula muscles) and muscle groups on the face (around the eyes, chin) and eyebrow muscles) by concentrating on contracting and relaxing these muscles. Step 4: Focusing on the muscle groups of the whole body, contracting and relaxing. Step 5: Opening the eyes slowly, trying to feel the feeling of comfort in the body (Turkish Psychologists Association Progressive Relaxation Exercises). |
|
No Intervention: Diabetic patients not applied progressive relaxation exercise
After explaining the purpose of the study and obtaining their verbal and written consents, a questionnaire form including the Beck Anxiety Scale and the World Health Organization Quality of Life Scale, in which the socio-demographic characteristics of the experimental and control group patients who will participate in the research, are asked, will be filled in face to face by the principal researcher.Then, a voice recording containing the commands for the application of the progressive relaxation exercise will be sent to the phone of the volunteer patients in this group and/or their relatives, and they will be informed about how to apply it.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Beck Anxiety Scale
Time Frame: 4 weeks
|
Progressive relaxation exercise was applied to the patients for 4 weeks.
After the application, anxiety scores were determined with the Back Anxiety Scale and the results were recorded.
|
4 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
World Health Organization Quality of Life Scale
Time Frame: 4 weeks
|
Progressive relaxation exercise was applied to the patients for 4 weeks.
After the application, quality of life scores were determined with the World Health Organization Quality of Life Scale and the results were recorded.
|
4 weeks
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- KahramanmarasIstiklalU
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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