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Fascial Manipulation on Scapulohumeral Rhythm and Proprioception in Patients With Rotator Cuff Tendinitis.

NCT07389252 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 32

Last updated 2026-02-05

No results posted yet for this study

Summary

The aim of this randomized controlled trial is to find the effectiveness of Fascial Manipulation on Scapulohumeral Rhythm and Proprioception in Patients with Rotator cuff tendinitis

Conditions

  • Rotator Cuff Tendinitis

Interventions

OTHER

Fascial manipulation technique

In initially step the patient in prone position and therapist approach on the same side of the treatment limb. Use the thumb by applying the pressure on the side of the target muscle. The treatment sequence will begin with thumb gradually involve the finger. A single treatment consists of a series of specific sequences of these moves with frequent pauses 2 to 5 minutes. Treatment session duration 15-30 minutes occur 2 days per week, for 4 weeks. Week 1(Fascial Manipulation on the targeted muscle for 5 minutes) week 2(Fascial Manipulation on the targeted muscle for 10 minutes) week 3(Fascial Manipulation on the targeted muscle for 15 minutes) week 4 (Fascial Manipulation on the targeted muscle for 20 minutes) Conventional PT including 1- hot pack (for 15 minutes)2- Periscapular exercises, a. shoulder shrug exercise (3 sets of 10 reps.) b. prone arm hangs (3 sets of 10 reps) 3- shoulder proprioception exercises a. Ball throws (30 reps) six times

OTHER

Conventional PT

Conventional PT including 1- hot pack (for 15 minutes)2- Periscapular exercises, a. shoulder shrug exercise (3 sets of 10 reps.) b. prone arm hangs (3 sets of 10 reps) 3- shoulder proprioception exercises a. Ball throws (30 reps) six times b. abc's on wall exercise 4- Shoulder stability exercises a. Ts Ys exercise (3 sets) b. side-lying external rotations (3 sets of 10 reps.) Total duration is 3 sessions per week for 4 consecutive weeks.

Sponsors & Collaborators

  • Riphah International University

    lead OTHER

Principal Investigators

  • Ramsha Tariq, MS-OMPT · Riphah International University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
20 Years
Max Age
45 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-08-30
Primary Completion
2025-12-30
Completion
2025-12-30

Countries

  • Pakistan

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07389252 on ClinicalTrials.gov