- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05344131
Investigation of the Effectiveness of a Biopsychosocial-Based Exercise Model in Rheumatic Diseases: A Mixed Methods Research With Patients' Perspectives
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Ankara, Turkey
- Hacettepe University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- patients diagnosed rheumatic diseases
- 18 years and over
Exclusion Criteria:
- presence of infection and fever, deformity that does not allow exercise, cardiopulmonary disorders, uncontrolled endocrine system diseases, and severe psychiatric illnesses.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: The quantitative part of the study (BETY exercise group)
intervention group Bilişsel Egzersiz Terapi Yaklaşımı (BETY, Cognitive Exercise Therapy Approach) is a group exercise method that conforms to the biopsychosocial model. Exercise dosage is 60 minute three days a week. |
Biopsychosocial approach
|
|
No Intervention: The quantitative part of the study (Control group)
Control group No intervention
|
|
|
Experimental: The qualitative part of the study
Regularly participated in the BETY program for at least one year Bilişsel Egzersiz Terapi Yaklaşımı (BETY, Cognitive Exercise Therapy Approach) is a group exercise method that conforms to the biopsychosocial model. Exercise dosage is 60 minute three days a week. |
Biopsychosocial approach
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Qualitative methods
Time Frame: after minimum one year participated BETY group
|
We aimed to complete qualitative semi-structured interviews to investigate biopsychosocial perspectives of patients with rheumatic diseases in each arm of the study.
Two pre-prepared interview topic guides were developed collaboratively by the research team with the project steering group which included lay members.
|
after minimum one year participated BETY group
|
|
Quantitative methods - Assessment of biopsychosocial status Bilişsel Egzersiz Terapi Yaklaşımı-Biopsychosocial Questionnaire (BETY-BQ)
Time Frame: before -12 weeks after.
|
The scale consists of 30 items.
The scoring of the scale was made using a 5-point Likert system.
Each question is scored as "No never: 0 Yes rarely: 1 Yes sometimes: 2 Yes often: 3 Yes always: 4" and gives a total score over 30 items.
A high score means that the biopsychosocial situation is 'bad'.
|
before -12 weeks after.
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Quantitative methods - Assessment of functionality Health Assessment Questionnaire (HAQ)
Time Frame: before -12 weeks after.
|
The functional status of the patients was determined by the Health Assessment Questionnaire.
The 20-question scale has 8 subtitles that include dressing, sitting, eating, walking, hygiene, reaching out, grasping, and daily life activities.
Each answer is scored between 0 and 3 points.
It means "0 = Without difficulty, 1 = A little difficult, 2 = Very difficult and 3 = I can never do it".
The total score is the average score derived from 8 points for each category.High score indicates low functional status.
|
before -12 weeks after.
|
|
Quantitative methods - Assessment of emotional status Hospital Anxiety and Depression Scale (HADS)
Time Frame: before -12 weeks after.
|
The anxiety and depression of the patients was determined by Hospital Anxiety and Depression Scale (HADS).
This questionnaire is consisting of 14 questions with 4 options.
The higher the score, the higher the anxiety and depression levels.
|
before -12 weeks after.
|
|
Quantitative methods - Assessment of quality of life Short Form 36 Health Survey Questionnaire (SF-36)
Time Frame: before -12 weeks after.
|
The quality of life of the patients was evaluated with the SF-36 scale.
Separate scores are obtained for each sub-parameter and scores range from 0-100. 100 points indicate good health, 0 points indicate poor health
|
before -12 weeks after.
|
Collaborators and Investigators
Collaborators
Investigators
- Study Director: EDİBE Unal, Hacettepe University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
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
Additional Relevant MeSH Terms
Other Study ID Numbers
- Kahramanmaras SIU
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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