Effects of seven types of exercise in the treatment of rotator cuff-related shoulder pain (RCRSP): a systematic review and Bayesian network meta-analysis.
Wei Zhang, Minghui Du, Liang Xia...
https://pubmed.ncbi.nlm.nih.gov/41276811/Actively Recruiting
Led by Istanbul Nisantasi University · Updated on 2026-07-06
72
Participants Needed
1
Research Sites
52 weeks
Total Duration
Researchers are evaluating whether adding personalized contextual factors to an exercise program can improve pain and function in people with rotator cuff-related shoulder pain, a common condition causing shoulder discomfort and activity limitations. This randomized controlled trial compares two exercise programs to determine if including personalized elements enhances recovery, pain relief, autonomic nervous system regulation, psychological outcomes, exercise adherence, and therapeutic alliance. Participants will be randomly assigned to one of two groups. Both groups receive the same standardized, evidence-based exercise program twice a week for 12 weeks, including a structured home exercise plan. One group experiences a fixed, neutral delivery of the program, while the other group receives added personalized contextual features such as preferred music and lighting, choice between equivalent exercises, motivational feedback, supportive communication, and personalized progress tracking. The intervention period is followed by assessments extending to 12 months. Throughout the study, participants complete questionnaires assessing pain, function, psychological factors, and exercise adherence. Heart rate variability is measured to evaluate autonomic nervous system regulation. Researchers will measure outcomes at multiple time points, including baseline, during treatment, and up to one year after. The trial aims to provide insight into the impact of contextual personalization on exercise therapy outcomes for shoulder pain.
CONDITIONS
Contextually Enhanced Exercise Programs for Rotator Cuff-Related Shoulder Pain
O
Onur Atakan Sekibağ, PhD (c)
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Istanbul Nisantasi University
Lead Sponsor
Istanbul University - Cerrahpasa
Collaborating Sponsor
You may qualify if you...
You will not qualify if you...
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - 12 weeks
Participants attend supervised exercise sessions twice weekly for 12 weeks and follow a structured home exercise program. They receive either a fixed or personalized contextual exercise program.
Twice-weekly supervised sessions
Duration - 12 months
Participants are followed for 12 months after treatment to assess pain, function, psychological factors, and autonomic nervous system regulation.
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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https://pubmed.ncbi.nlm.nih.gov/29357856/Istanbul Nisantasi University
Lead Sponsor
Istanbul University - Cerrahpasa
Collaborating Sponsor