Status:
RECRUITING
Strength Training and Proprioceptive Stimulation on Pain, Function, Quality of Life, Sleep Quality, and Psychosocial Factors in Older Adults With Shoulder Pain
Lead Sponsor:
University of Jaén
Conditions:
Shoulder Pain
Eligibility:
All Genders
60+ years
Phase:
NA
Brief Summary
A single-blind randomized clinical trial with a pretest posttest design is proposed in adults over 60 years of age with chronic shoulder pain due to rotator cuff involvement. Participants will be divi...
Eligibility Criteria
Inclusion
- People over 60 years of age.
- Be able to understand the instructions and answer the questionnaires designed for this study, as well as participate in the established physical tests.
- People with rotator cuff-related shoulder pain (RCSRP) of at least 3 months' duration.
- Sign informed consent to participate in the study.
- Possible medical diagnoses to categorize you as RCSRP:
- Subacromial syndrome or subacromial pain syndrome.
- Subacromial impingement.
- Rotator cuff tendinopathy/tendinitis/tendinosis.
- Subdeltoid/subacromial bursitis.
- Non-traumatic partial tears of a rotator cuff tendon affecting less than 50% of the tendon thickness.
- Mild/moderate intrasubstance rotator cuff tears.
Exclusion
- Complete/massive rotator cuff tears.
- Corticosteroid injections within the last 6 weeks.
- Recent surgery on that shoulder or planned surgery within the next 3 months.
- Bilateral shoulder pain.
- Presence of glenohumeral fractures or osteoarthritis confirmed by radiographic examination.
- Psychiatric illnesses or central or peripheral neurological disorders that make it difficult to grasp, cooperate, or follow instructions during the procedure.
- Individuals with an absolute contraindication to moderate-to-high-intensity physical exercise based on prior medical testing.
- Presence of severe difficulties with gait, balance, or functional activity, or hearing or vestibular disorders that prevent the performance of the prescribed exercises.
- Visual disturbances that cannot be corrected with glasses, contact lenses, or surgery.
- Being enrolled in another physical exercise or treatment program during the study.
Key Trial Info
Start Date :
September 18 2025
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
December 19 2025
Estimated Enrollment :
80 Patients enrolled
Trial Details
Trial ID
NCT07184242
Start Date
September 18 2025
End Date
December 19 2025
Last Update
November 26 2025
Active Locations (1)
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1
ICOT rehabilitation centers
Las Palmas de Gran Canaria, Spain