The effect of mulligan mobilization technique application in addition to conventional physiotherapy on pain and joint range of motion in people with neck pain.
Ozge Ozlu, Mustafa Sahin
https://pubmed.ncbi.nlm.nih.gov/38876630/Actively Recruiting
Led by Kirsehir Ahi Evran Universitesi · Updated on 2026-06-08
75
Participants Needed
1
Research Sites
N/A
Total Duration
Rotator cuff lesions are a common cause of shoulder pain and reduced function, especially in middle-aged and older adults. This trial investigates the effects of Mobilization with Movement MWM, a manual therapy technique, on pain, function, and shoulder joint position sense in people with rotator cuff lesions. Researchers aim to find out if MWM offers benefits beyond conventional physiotherapy or task-oriented virtual reality training for improving shoulder health and proprioception. Participants with rotator cuff lesions will be randomly assigned to one of three groups the MWM group receiving manual therapy combined with active, pain-free shoulder movements the conventional physiotherapy group receiving standard exercises and physical therapy without MWM techniques or the control group engaging in task-oriented training through virtual reality exercises simulating daily activities. Treatments will be delivered by trained physiotherapists following standardized protocols over an 8-week intervention period. Participants will be evaluated before and after the intervention using the Quick Disabilities of the Arm, Shoulder and Hand QuickDASH questionnaire to assess functional disability, pain intensity scales, and a shoulder joint position sense test involving active repositioning with a laser pointer. The study will also monitor changes in proprioceptive accuracy and shoulder function to determine MWMs role in conservative rehabilitation. All procedures are conducted under ethical standards with informed consent, and the trial concludes with assessments after the 8-week program.
CONDITIONS
Effect of Mobilization With Movement in Patients With Rotator Cuff Lesions
Ö
Ömer Faruk Özçelep, PhD
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Kirsehir Ahi Evran Universitesi
Lead Sponsor
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Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 8 weeks
Participants receive one of three interventions: Mobilization with Movement manual therapy, conventional physiotherapy, or task-oriented virtual reality training aimed at improving shoulder function and reducing pain.
Multiple therapy sessions per week during the 8-week intervention period
Duration - Immediately after the 8-week intervention period
Participants undergo assessments to evaluate pain, functional status, and shoulder proprioception after completing the intervention.
1 visit (in-person) for post-intervention assessment
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
3
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Ozge Ozlu, Mustafa Sahin
https://pubmed.ncbi.nlm.nih.gov/38876630/Kirsehir Ahi Evran Universitesi
Lead Sponsor