Clinical Trial

Real Dry Needling and Placebo Dry Needling Applied With and Without Ultrasound Guidance on the Infraspinatus Muscle

Study acronym: DN-INFR-RCT
Not Yet Recruiting
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Record status
This record was last updated September 4, 2024 (before its estimated February 2025 completion). Its status may not reflect the trial's current state.
Summary
The infraspinatus muscle is one of the four muscles that form the rotator cuff. The dry needling technique involves inserting a sterile needle to stimulate a myofascial trigger point with the aim of reducing pain and increasing range of motion and quality of life. This technique can be performed using ultrasound guidance, which allows us to visualize the needle at all times, but it can also be done using anatomical landmarks. This study includes a self-directed exercise plan for rotator cuff tendinopathy. Variables such as strength, shoulder functionality level, grip strength, and active range of motion will be measured. As part of the intervention, two dry needling sessions will be performed, 14 days apart, along with two different exercise programs. Three measurements will be taken, and the intervention will last for 6 weeks. The sample will be divided into four equal groups: Group 1: ultrasound-guided real dry needling; Group 2: ultrasound-guided placebo dry needling; Group 3: non-ultrasound-guided real dry needling; and Group 4: non-ultrasound-guided placebo dry needling
Trial Details
NCT Number NCT06583707
Lead Sponsor University of Alcala
Conditions Tendinopathy, Rotator Cuff
Enrollment 76 participants
Start Date 2024-09-23
Primary Completion 2025-02 (estimated)
Study Completion 2025-03 (estimated)
Updated on ClinicalTrials.gov 2024-09-04