Is Gender a Factor in Patients With Subacromial Shoulder Pain?
Patients With Subacromial Shoulder Pain and Gender
1 other identifier
observational
65
1 country
1
Brief Summary
This study aimed to investigate the effects of gender on pain, functionality, range of motion, disability level and position sense parameters in patients with subacromial shoulder pain.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started Oct 2024
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
October 25, 2024
CompletedFirst Submitted
Initial submission to the registry
December 30, 2024
CompletedFirst Posted
Study publicly available on registry
January 6, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 22, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
September 17, 2026
April 20, 2026
April 1, 2026
1.8 years
December 30, 2024
April 17, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Visual Analog Scale
20 weeks
Secondary Outcomes (3)
Quick DASH
20 weeks
SPADI
20 weeks
The laser-pointer assisted angle reproduction test
20 weeks
Study Arms (1)
Study Group
Eligibility Criteria
The study will be conducted with patients who apply to Kırşehir Ahi Evran University Physical Therapy and Rehabilitation Center with complaints of shoulder pain and who meet the inclusion criteria.
You may qualify if:
- Being between the ages of 18-65
- Being diagnosed with unilateral subacromial impingement syndrome
- Not having received steroid injections or physical therapy for shoulder problems in the last 6 months
- Having painful shoulder pain for the last 3 months
- Being willing to participate in the study
You may not qualify if:
- Having a rheumatic, neurological, cardiovascular, psychiatric or systemic disorder
- Having a surgical operation on the shoulder, cervical and thoracic region
- Having a neurological deficit, fracture or history of fracture in the upper extremity
- Having cervical radiculopathy
- Having communication problems
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Kirsehir Ahi Evran University
Kırşehir, Merkez, 40100, Turkey (Türkiye)
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Lecturer Dr.
Study Record Dates
First Submitted
December 30, 2024
First Posted
January 6, 2025
Study Start
October 25, 2024
Primary Completion (Estimated)
August 22, 2026
Study Completion (Estimated)
September 17, 2026
Last Updated
April 20, 2026
Record last verified: 2026-04
Data Sharing
- IPD Sharing
- Will not share