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NCT06031857 Clinical Trial

Comparison of Kinesio Tape and Dry Needling for the Management of Rotator Cuff Tendinopathy: A Randomized Control Trial

Rotator Cuff Tendinopathy Clinical Trial

Official title:
Comparison of Kinesio Tape and Dry Needling for the Management of Rotator Cuff Tendinopathy: A Randomized Control Trial

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT06031857
Other study ID # 343
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 10, 2023
Est. completion date August 9, 2023

Study information
Verified date September 2023
Source Neuro Counsel Hospital, Pakistan
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Its a single blind RCT

Description:

Kinesio tape and dry needling were compared for the management of rotator cuff tendinopathy

Recruitment information / eligibility
Status Completed
Enrollment 40
Est. completion date August 9, 2023
Est. primary completion date August 9, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 25 Years to 50 Years
Eligibility Inclusion Criteria: - age between 25-50 years old - Both genders - Not any comorbidity Exclusion Criteria: - Parkinson disease - DM - HTN

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• kinesio tape
kinesio tape was applied over the specific muscle of rotator cuff
• Dry needling
dry needling was applied over the affected muscles

Locations
Country Name City State
Pakistan The Neurocouncil Clinic Islamabad Federal

Sponsors (2)
Lead Sponsor Collaborator
Neuro Counsel Hospital, Pakistan Rawal General and Dental hospital, Islamabad

Country where clinical trial is conducted

Pakistan, 

Outcome
Type Measure Description Time frame Safety issue
Primary PNS Pain numeric Scale consists of 10 scores. 0 means no pain and 10 means worst pain ever will be used to assess at baseline after 3 weeks
Primary SF-36 short form 36 is used to measure the quality of life. lower scores means lower quality of life and ligher score means better quality of life will be used to assess at baseline after 3 weeks
See also
  Status Clinical Trial Phase
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Not yet recruiting NCT05969652 - Comparison of the Effectiveness Heavy Slow Resistance and Eccentric Training in Rotator Cuff Tendinopathy N/A
Completed NCT05320419 - The Effect of Amniotic Membrane Injection as An Addition to Physical Therapy in Patients With Rotator Cuff Tear N/A
Completed NCT03454321 - IS'ECHO : Impact of Bursitis on the Efficacy of Subacromial Steroid Injection in Rotator Cuff Tendinopathy
Withdrawn NCT03032432 - A Dynamic Elastic Garment (DEG) in Patients With Rotator Cuff Tendinopathy Phase 4
Completed NCT05207384 - Comparison of Subacromial Ozone (O2-O3) and Corticosteroid Injections in the Treatment of Rotator Cuff Tendinopathy N/A
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Active, not recruiting NCT05124769 - PAin During Shoulder Exercise N/A
Completed NCT03104218 - Transcranial Direct Current Stimulation to Enhance Rehabilitation in Individuals With Rotator Cuff Tendinopathy N/A
Completed NCT01915979 - Effect of Plasma Rich in Growth Factors in Rotator Cuff Tendinopathy Phase 3
Not yet recruiting NCT02982460 - Effects of Isoinertial Training on Rotator Cuff Tendinopathy N/A
Recruiting NCT05758415 - Study of Efficacy and Safety of Secukinumab in Participants With Moderate-severe Rotator Cuff Tendinopathy Phase 3
Recruiting NCT05722522 - Study of Efficacy and Safety of Secukinumab in Participants With Moderate-severe Rotator Cuff Tendinopathy Phase 3
Completed NCT01423682 - The Influence of Eccentric Training on the Volume and Vascularisation of the Rotator Cuff in Patients With Rotator Cuff Tendinopathy and Healthy Subjects N/A