Tendinitis Clinical Trials

Find Tendinitis Clinical Trials Near You

The Effect of an Exercise Program Based on Attentional Focus Shifting on Clinical Outcomes in Rotator Cuff Related Shoulder Pain

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The aim of this clinical trial is to investigate the effects of an attention shift-based rehabilitation program on clinical outcomes in individuals with rotator cuff-related shoulder pain (RCRSP). The study will evaluate the effects of an attention shift approach, in which motor tasks targeting regions outside the shoulder are performed concurrently with standard shoulder exercises, on pain, functional status, and pain catastrophizing. These results will be compared with those of a standard shoulder rehabilitation program. The main questions this study aims to answer are: Is there a difference in pain levels between individuals with RCRSP who participate in an attention shift-based rehabilitation program and those who participate in a standard exercise program? Is there a difference between these two rehabilitation approaches in terms of shoulder function and pain catastrophizing? Participants will: Be randomly assigned to either an attention shift-based rehabilitation group or a standard shoulder rehabilitation group Participate in supervised exercise sessions twice per week for 6 weeks Attend sessions lasting approximately 60-75 minutes Undergo clinical assessments at baseline and at week 6

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 65
Healthy Volunteers: f
View:

• Having symptoms persisting for at least 3 months

• Experiencing pain intensity of at least 3 on the Numeric Pain Rating Scale (NPRS) during activity

• Presence of a painful arc during shoulder flexion or abduction

• Positive Neer test or Hawkins-Kennedy test

• Pain provoked by resisted external rotation/abduction of the humerus, or a positive Jobe (Empty Can) test

• Having a clinical diagnosis of subacromial pain syndrome, rotator cuff tendinopathy, subacromial bursitis, or symptomatic partial/full-thickness rotator cuff tear

• Being able to understand and complete questionnaires in Turkish

Locations
Other Locations
Turkey
Istanbul University-Cerrahpasa
RECRUITING
Istanbul
Contact Information
Primary
Rezzan Atay, Bachelor's degree
rezzan.atay@ogr.iuc.edu.tr
90+ 505 485 75 49
Time Frame
Start Date: 2026-05-15
Estimated Completion Date: 2027-06-15
Participants
Target number of participants: 46
Treatments
Experimental: Attention Shift-Based Rehabilitation Group
Participants in this group will receive a supervised shoulder rehabilitation program combined with motor tasks targeting regions outside the shoulder. These additional tasks are designed to shift attention away from the painful shoulder region. Exercises will be performed twice per week for 6 weeks, with each session lasting approximately 60-75 minutes. All participants will also receive standardized patient education.
Active_comparator: Standard Exercise Group
Participants in this group will receive a standardized shoulder rehabilitation program consisting of conventional therapeutic exercises. No attention-shifting or additional motor tasks will be included. The program will be administered twice per week for 6 weeks, with each session lasting approximately 60-75 minutes. All participants will also receive standardized patient education.
Related Therapeutic Areas
Sponsors
Leads: Istanbul University

This content was sourced from clinicaltrials.gov

Similar Clinical Trials