Clinical Trial

Effect of Dry Needling on Gluteus Medius Contraction in Greater Trochanteric Pain Syndrome: a Pilot RCT Protocol

Not Yet Recruiting
View on ClinicalTrials.gov →
Record status
This record was last updated September 4, 2024 (before its estimated September 8, 2025 completion). Its status may not reflect the trial's current state.
Summary
Grater trochanteric pain syndrome is a hip related pathology that causes lateral hip pain and lack of strength in abductor muscles such as the gluteus medius, which hinders functional activities and daily life, such as standing, walking, sleeping on the affected side... Lack of strength and eccentric control of the gluteus medius may be related to the apparition of myofascial trigger points that are susceptible to treatment with dry needling. In this study, two groups of patients with greater trochanteric pain syndrome will be treated with dry needling, some of them with real dry needling, and others with sham dry needling. Ultrasound will be used to assess whether real dry needling in the pelvitrochanteric musculature improves the potential contraction of the gluteus medius, in relation to a baseline measurement and to sham dry needling. This study is a randomised clinical trial protocol, pilot study, so there will be no previous references for the sample of both study groups. 3 dry needling interventions will be performed in 3 consecutive weeks, leaving 1 week between each intervention. Data will be collected for the variables to be investigated (potential contraction, pain, function, strength…) before the first intervention, after each intervention, 1 month after the last intervention and at 3 months.
Trial Details
NCT Number NCT06584500
Lead Sponsor University of Alcala
Conditions Greater Trocantheric Pain Syndrome
Enrollment 40 participants
Start Date 2024-10-15
Primary Completion 2025-09-08 (estimated)
Study Completion 2025-11-08 (estimated)
Updated on ClinicalTrials.gov 2024-09-04