Skip to main content
Clinical Trials/NCT06213584
NCT06213584
Completed
Not Applicable

The Effectiveness of Mulligan and Proprioceptive Neuromuscular Fasciliation Techiniques in Rotator Cuff Pathology: A Randomized Controlled Double-blind Study.

Istanbul University - Cerrahpasa (IUC)1 site in 1 country60 target enrollmentJanuary 5, 2020

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Rotator Cuff Injuries
Sponsor
Istanbul University - Cerrahpasa (IUC)
Enrollment
60
Locations
1
Primary Endpoint
angle repetition test
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

The aim of this study is to investigate the effects of Mulligan Mobilization techniques, Mobilization with Movement (MWMs) and Proprioceptive Neuromuscular Facilitation (PNF) techniques, Hold-Relax Active Movement Technique, on pain, normal joint range of motion, proprioception, scapular dyskinesia and functional status in individuals with rotator cuff syndrome.

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).

Registry
clinicaltrials.gov
Start Date
January 5, 2020
End Date
March 25, 2022
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Istanbul University - Cerrahpasa (IUC)
Responsible Party
Principal Investigator
Principal Investigator

Gamze Aydin

Istanbul Okan University

Istanbul University - Cerrahpasa (IUC)

Eligibility Criteria

Inclusion Criteria

  • between the ages of 25-75,
  • diagnosed with rotator cuff syndrome,
  • patients who did not have any obstacle to the evaluation parameters

Exclusion Criteria

  • having had shoulder surgery,
  • presence of scoliosis,
  • presence of cardiac pacemaker,
  • history of recent myocardial infarction,
  • presence of malignancy,
  • corticosteroid treatment within the last 3 months

Outcomes

Primary Outcomes

angle repetition test

Time Frame: 12 months

proprioception

lateral scapular glide test

Time Frame: 12 months

presence of scapular dyskinesia

goniometer

Time Frame: 12 months

shoulder range of motion

visual analog scale

Time Frame: 12 months

shoulder pain intensity

Western Ontario Rotator Cuff Index

Time Frame: 12 months

functionality

SF-36

Time Frame: 12 months

quality of life

Study Sites (1)

Loading locations...

Similar Trials