Mulligan and Proprioceptive Neuromuscular Fasciliation Techiniques in Rotator Cuff Pathology
NCT ID: NCT06213584
Last Updated: 2024-01-19
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
60 participants
INTERVENTIONAL
2020-01-05
2022-03-25
Brief Summary
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A total of 60 people were included in the study: 20 participants in the censervative rehabilitation group (Conservative Treatment), 20 participants in the Treatment A (Mulligan Mobilization Application) Group, and 20 participants in the Treatment B (PNF Application) Group. Individuals were treated for 5 days for 4 weeks. Pain before and after treatment with Visual Analog Scale; joint range of motion with goniometer; With proprioception Angle Repetition Test; Scapular dyskinesia with Lateral Scapular Slide Test; quality of life with SF-36; shoulder functionality was assessed with the Western Ontario Rotator Cuff Scale (WORC).
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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mulligan mobilization
Mulligan mobilization techniques
conservative rehabilitation
Hotpack + TENS + streching exercises
mullgan mobilization techniques
Passive mobilization techniques during active movements
pnf
Proprioceptive neuromuscular fasciliation techniques
conservative rehabilitation
Hotpack + TENS + streching exercises
pnf
hold relax active movements
conservative rehabilitation
Conservative rehabilitation
conservative rehabilitation
Hotpack + TENS + streching exercises
Interventions
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conservative rehabilitation
Hotpack + TENS + streching exercises
mullgan mobilization techniques
Passive mobilization techniques during active movements
pnf
hold relax active movements
Eligibility Criteria
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Inclusion Criteria
* diagnosed with rotator cuff syndrome,
* patients who did not have any obstacle to the evaluation parameters
Exclusion Criteria
* presence of scoliosis,
* presence of cardiac pacemaker,
* history of recent myocardial infarction,
* presence of malignancy,
* corticosteroid treatment within the last 3 months
25 Years
75 Years
ALL
Yes
Sponsors
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Istanbul University - Cerrahpasa
OTHER
Responsible Party
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Gamze Aydin
Istanbul Okan University
Principal Investigators
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Gamze AYDIN
Role: PRINCIPAL_INVESTIGATOR
Okan University
Locations
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Istanbul Okan University
Istanbul, , Turkey (Türkiye)
Countries
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Other Identifiers
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IOU
Identifier Type: -
Identifier Source: org_study_id
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