CClinicalTrials.gg
CompletedNCT07528807EPAPUpdated Oct 1, 2026

Exercise, Pain Beliefs, and Activity Patterns in Musculoskeletal Pain

An observational study in Musculoskeletal Pain - Acute and Subacute Conditions, Exercise (EX) and Beliefs, sponsored by Istinye University. Completed at 1 site in Turkey (Türkiye). Open to participants aged 18 Years to 65 Years. Per ClinicalTrials.gov, last updated 2026-10-01.

Sponsored by Istinye University · Observational

Updated Oct 1, 2026Now CompletedStudy completion moved+1 moreGo to Updates ↓
Study type
Observational
Model
Other
Time perspective
Prospective
Enrollment
60
Ages
18 Years to 65 Years
Sex
All
01

Study summary

This observational study aims to investigate the relationship between exercise benefits and barriers, pain beliefs, and activity patterns in individuals experiencing musculoskeletal pain. Participants will complete questionnaires about their pain, exercise habits, and daily activity patterns. The study does not involve any interventions or treatments. The purpose is to better understand how beliefs and perceived barriers influence physical activity in people with musculoskeletal pain, which may help inform future strategies to improve exercise participation and overall well-being.

Read the 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.

02

Conditions studied

  • Musculoskeletal Pain - Acute and Subacute Conditions
  • Exercise (EX)
  • Beliefs
  • Activity Level

Keywords

  • Musculoskeletal Pain
  • Barriers to Physical Activity
  • Pain Beliefs
  • Activity Patterns
03

In context

Motor Activity

2,426 studies on the registry are indexed under Motor Activity; 1,161 are open to participants now.

This study's enrollment of 60 is below the median of 100 across 292 observational studies indexed under Motor Activity.

Browse Motor Activity studies →

Lead sponsor

Istinye University is the lead sponsor of 207 studies on the registry; 88 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

The study will include adults aged 18-65 years who have experienced musculoskeletal pain within the past 6 months. Participants must be able to read and understand Turkish and provide informed consent. Individuals with acute trauma, recent surgery, severe cardiovascular, neurological, or psychiatric conditions, cognitive impairments, or who are pregnant will be excluded.

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

Exclusion Criteria:

-

05

Study design

Observational model
Other
Time perspective
Prospective
Enrollment
60 participants (actual)
Patient registry
No

Groups and cohorts

  • 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.

    Other: This is an observational study. No interventions or treatments are administered.

Interventions

  • OtherThis is an observational study. No interventions or treatments are administered.

    Not applicable - observational study, no interventions administered

06

What researchers measure

Primary outcomes

  1. Pain Beliefs (PBQ)

    Participants' perceived benefits of and barriers to exercise will be assessed using the Exercise Benefits/Barriers Scale.

    Time frame: Single assessment at survey completion

Secondary outcomes

  1. Exercise Benefits and Barriers (EBBS)

    Participants' perceived benefits of and barriers to exercise will be assessed using the Exercise Benefits/Barriers Scale.

    Time frame: Single assessment at survey completion

  2. Pain-Related Activity Patterns (POAM-P)

    Participants' activity patterns in relation to pain and pain management strategies will be measured using the Pain-Related Activity Patterns Questionnaire .

    Time frame: Single assessment at survey completion

  3. Demographic Data

    Age, sex, education level, and occupation will be collected using a demographic questionnaire.

    Time frame: Single assessment at survey completion

07

Study locations

1 site
  • İstinye University Faculty of Health Sciences, Department of Physiotherapy and Rehabilitation
    Istanbul, Turkey (Türkiye)
08

References and documents

Individual participant data

Plan to share: No — The study will not share individual participant data to protect participants' privacy and confidentiality. Data include sensitive health information, and sharing it could risk identification of participants.

No publications or documents are linked to this record.

09

Updates

1 registry update since Sep 25, 2026
Status
Recruiting→Completed
changed Oct 1, 2026
Study completion
Dec 1, 2026→Sep 1, 2026 (actual)
Oct 1, 2026
Enrollment
55 (estimated)→60 (actual)
Oct 1, 2026
Show all 1 update
  1. Oct 1, 2026
    Recruiting→Completed
    Study completion Dec 1, 2026→Sep 1, 2026 (now actual)
    Enrollment 55 (estimated)→60 (actual)
    + 3 other changes: verification date, contact details and site details

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07528807
Lead sponsor
Istinye University
Responsible party
Elif Dilara Durmaz (Doctoral Researcher, Principal Investigator, Istinye University) — Principal investigator
First posted
Apr 14, 2026
Start date
Apr 26, 2026
Primary completion
Apr 27, 2026
Completion
Sep 1, 2026
Last update
Oct 1, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Sep 2026. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion