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Not Yet RecruitingNCT06823206

Effects of Movement Representation Techniques with Sensorimotor Training for Rotator Cuff Related Shoulder Pain

Effects of Movement Representation Techniques with Sensorimotor Training for Rotator Cuff Related Shoulder Pain: a Randomised Controlled Trial

Status
Not Yet Recruiting
Phase
N/A
Study type
Interventional
Enrollment
122 (estimated)
Sponsor
The Hong Kong Polytechnic University · Academic / Other
Sex
All
Age
50 Years
Healthy volunteers
Not accepted

Summary

The aim of this study is to evaluate the efficacy of 12 weeks of sensorimotor training with movement representation techniques for reducing pain intensity in people with rotator cuff related shoulder pain, relative to standard care. Besides, the secondary aim of this study is to explore the mechanisms underlying the effects of central mechanism treatment in people with rotator cuff related shoulder pain. A total of 122 older adults aged 50 or above with the presence of shoulder pain for more than three months will be recruited and randomized into 12-weeks of movement representation techniques with sensorimotor training vs. standard care. Shoulder pain and disability Index (SPADI), changes in primary motor cortex (M1) using brain MRI, changes in subacromial space using ultrasound imaging, Widespread Pain Index (WPI), Pain Catastrophising Scale (PCS), and Fear-avoidance Beliefs questionnaires (FABQ) will be assessed at baseline and 12-week post intervention.

Conditions

Interventions

TypeNameDescription
OTHERSensorimotor training with movement representation techniquesSensorimotor training will be implemented with movement representation techniques using a standardized retraining sequence of a shoulder control exercise during arm elevation with 3 phases: Phase 1: Action Observation Training; Phase 2: Mirror therapy; and Phase 3: Sensorimotor training of the involved arm. Each session will last 60 minutes, with one supervised intervention session over the 12 weeks.

Timeline

Start date
2025-03-01
Primary completion
2027-12-01
Completion
2027-12-01
First posted
2025-02-12
Last updated
2025-02-12

Source: ClinicalTrials.gov record NCT06823206. Inclusion in this directory is not an endorsement.