Skip to content

Blood Flow Restriction Therapy and Gua Sha Therapy in Rotator Cuff Tendinopathy Patients

Effects of Blood Flow Restriction Therapy and Gua Sha Therapy in Rotator Cuff Tendinopathy Patients

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07587502
Enrollment
34
Registered
2026-05-14
Start date
2025-08-01
Completion date
2026-04-30
Last updated
2026-05-19

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

Conditions

Rotator Cuff Syndrome, Rotator Cuff Tendinopathy

Keywords

Rotator Cuff Tendinopathy, Blood flow restriction therapy, Gua Sha Scraping, Muscle Hypertrophy

Brief summary

The goal of study is to improve shoulder tendinopathy. By comparing advanced blood flow restriction with traditional Gua sha scraping, it can be identified which therapy is more effective at restoring functional movement and comfort for patients

Detailed description

This six-week study randomly assigned 34 patients with rotator cuff tendinopathy to either a Blood Flow Restriction group or a Gua sha scraping group. Using pain and disability scales, we monitored 17 participants per group to determine which treatment offered better functional recovery

Interventions

OTHERBlood Flow Restriction

17 patients were administered Blood Flow restriction Therapy along with Therapeutic Exercises twice per week for 6 weeks.

OTHERGua Sha Scraping Therapy

17 patients were administered Gua Sha Therapy along with Therapeutic Exercises twice per week for 6 weeks.

Sponsors

Elite College of Management Sciences, Gujranwala, Pakistan
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* patients having age group 18 to 60 years * patients positive for Clinical Tendinopathy * patients having positive painful arc

Exclusion criteria

* patients having any systemic Disorders * patients having fractures and dislocations * Pregnant Females * Large Rotator Cuff Tears

Design outcomes

Primary

MeasureTime frameDescription
Shoulder Pain and Disability Index (SPADI)6 weeksThe Shoulder Pain and Disability Index is a 13-item, patient-reported outcome measure used to evaluate the severity of shoulder pain and the resulting impact on functional activities. Patients rate each item on a scale from 0 to 10, where 0 represents "no pain/no difficulty" and 10 represents "worst pain imaginable/so difficult it requires help
Visual Analogue Scale6 weeksThe Visual Analogue Scale is a single-item measurement instrument used to quantify subjective pain experiences in this study. it consists of a 0-100 mm scale in which 0 means no pain and 100 means worst possible pain.

Countries

Pakistan

Contacts

STUDY_DIRECTORUsman Iqbal Janjua, PhD Rehabilitation Sciences

Elite College of Management Sciences, Gujranwala

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 20, 2026