NCT06213584

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).

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
60

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Jan 2020

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 5, 2020

Completed
1.2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 5, 2021

Completed
1.1 years until next milestone

Study Completion

Last participant's last visit for all outcomes

March 25, 2022

Completed
1.8 years until next milestone

First Submitted

Initial submission to the registry

January 10, 2024

Completed
9 days until next milestone

First Posted

Study publicly available on registry

January 19, 2024

Completed
Last Updated

January 19, 2024

Status Verified

January 1, 2024

Enrollment Period

1.2 years

First QC Date

January 10, 2024

Last Update Submit

January 10, 2024

Conditions

Rotator Cuff Injuries

Keywords

rotator cuff injuriesmulligan mobilizationproprioceptive neuromuscular fascilitationpainfunctionalityquality of life

Outcome Measures

Primary Outcomes (6)

  • goniometer

    shoulder range of motion

    12 months

  • visual analog scale

    shoulder pain intensity

    12 months

  • angle repetition test

    proprioception

    12 months

  • lateral scapular glide test

    presence of scapular dyskinesia

    12 months

  • Western Ontario Rotator Cuff Index

    functionality

    12 months

  • SF-36

    quality of life

    12 months

Study Arms (3)

mulligan mobilization

EXPERIMENTAL

Mulligan mobilization techniques

Other: conservative rehabilitationOther: mullgan mobilization techniques

pnf

EXPERIMENTAL

Proprioceptive neuromuscular fasciliation techniques

Other: conservative rehabilitationOther: pnf

conservative rehabilitation

EXPERIMENTAL

Conservative rehabilitation

Other: conservative rehabilitation

Interventions

conservative rehabilitationOTHER

Hotpack + TENS + streching exercises

conservative rehabilitationmulligan mobilizationpnf
mullgan mobilization techniquesOTHER

Passive mobilization techniques during active movements

mulligan mobilization
pnfOTHER

hold relax active movements

pnf

Eligibility Criteria

Age25 Years - 75 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

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

You may not qualify if:

  • 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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Istanbul Okan University

Istanbul, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Rotator Cuff InjuriesPain

Condition Hierarchy (Ancestors)

RuptureWounds and InjuriesShoulder InjuriesTendon InjuriesNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Officials

  • Gamze AYDIN

    Okan University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Istanbul Okan University

Study Record Dates

First Submitted

January 10, 2024

First Posted

January 19, 2024

Study Start

January 5, 2020

Primary Completion

March 5, 2021

Study Completion

March 25, 2022

Last Updated

January 19, 2024

Record last verified: 2024-01

Data Sharing

IPD Sharing
Will not share

Locations

TU(1)