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Mulligan and Proprioceptive Neuromuscular Fasciliation Techiniques in Rotator Cuff Pathology

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06213584
Enrollment
60
Registered
2024-01-19
Start date
2020-01-05
Completion date
2022-03-25
Last updated
2024-01-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Rotator Cuff Injuries

Keywords

rotator cuff injuries, mulligan mobilization, proprioceptive neuromuscular fascilitation, pain, functionality, quality of life

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).

Interventions

Hotpack + TENS + streching exercises

OTHERmullgan mobilization techniques

Passive mobilization techniques during active movements

OTHERpnf

hold relax active movements

Sponsors

Istanbul University - Cerrahpasa
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
25 Years to 75 Years
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frameDescription
goniometer12 monthsshoulder range of motion
visual analog scale12 monthsshoulder pain intensity
angle repetition test12 monthsproprioception
lateral scapular glide test12 monthspresence of scapular dyskinesia
Western Ontario Rotator Cuff Index12 monthsfunctionality
SF-3612 monthsquality of life

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026