- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07528807
Exercise, Pain Beliefs, and Activity Patterns in Musculoskeletal Pain (EPAP)
Investigation of the Relationship Between Exercise Benefits and Barriers, Pain Beliefs, and Activity Patterns in Individuals Experiencing Musculoskeletal Pain
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
This observational study will include individuals experiencing musculoskeletal pain. Participants will be asked to complete a series of questionnaires assessing pain intensity, exercise benefits and barriers, pain-related beliefs, and activity patterns. The study aims to explore the relationships among these factors to better understand how pain perceptions and perceived barriers affect physical activity.
No interventions, treatments, or medications will be administered as part of this study. All data will be collected confidentially, and participation is voluntary. Participants may withdraw from the study at any time without any consequences. The findings of this research may help inform future strategies to improve exercise adherence and overall quality of life in individuals with musculoskeletal pain.
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Elif Dilara durmaz Istinye University, Turkey
- Phone Number: 0905072367034
- Email: elifdilaradurmaz@gmail.com
Study Locations
-
-
-
Istanbul, Turkey (Türkiye)
- Recruiting
- İstinye University Faculty of Health Sciences, Department of Physiotherapy and Rehabilitation
-
Contact:
- elif dilara durmaz
- Phone Number: +90 5072367034
- Email: elifdilaradurmaz@gmail.com
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
Adults aged 18-65 years Experiencing musculoskeletal pain (must have experienced musculoskeletal pain within the past 6 months) Voluntarily agree to participate and provide signed informed consent Able to read and understand Turkish (to complete questionnaires accurately)
Exclusion Criteria Younger than 18 years or older than 65 years Acute trauma, recent surgery, or infection causing temporary musculoskeletal pain Severe cardiovascular, neurological, or psychiatric disorders unrelated to musculoskeletal pain Pregnant women (due to potential physiological changes affecting musculoskeletal pain) Cognitive or mental impairments preventing accurate completion of study questionnaires
Exclusion Criteria:
-
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Single Cohort
All participants experiencing musculoskeletal pain will complete questionnaires assessing pain intensity, exercise benefits and barriers, pain beliefs, and activity patterns.
No interventions or treatments will be administered.
|
Not applicable - observational study, no interventions administered
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Pain Beliefs (PBQ)
Time Frame: Single assessment at survey completion
|
Participants' perceived benefits of and barriers to exercise will be assessed using the Exercise Benefits/Barriers Scale.
|
Single assessment at survey completion
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Demographic Data
Time Frame: Single assessment at survey completion
|
Age, sex, education level, and occupation will be collected using a demographic questionnaire.
|
Single assessment at survey completion
|
|
Exercise Benefits and Barriers (EBBS)
Time Frame: Single assessment at survey completion
|
Participants' perceived benefits of and barriers to exercise will be assessed using the Exercise Benefits/Barriers Scale.
|
Single assessment at survey completion
|
|
Pain-Related Activity Patterns (POAM-P)
Time Frame: Single assessment at survey completion
|
Participants' activity patterns in relation to pain and pain management strategies will be measured using the Pain-Related Activity Patterns Questionnaire .
|
Single assessment at survey completion
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
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
Additional Relevant MeSH Terms
Other Study ID Numbers
- EPAP 24-314
- No secondary ID (Other Identifier: Istinye University Human Research Ethics Committee)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
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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