Ignite Creation Date:
2024-10-26 @ 3:39 PM
Last Modification Date:
2024-10-26 @ 3:39 PM
Study NCT ID:
NCT06584500
Status:
NOT_YET_RECRUITING
Last Update Posted:
None
First Post:
2024-09-02
Brief Title:
Effect of Dry Needling on Gluteus Medius Contraction in Greater Trochanteric Pain Syndrome a Pilot RCT Protocol
Sponsor:
None
Organization:
None
Study Overview
Official Title:
Analysis of the Effect of Dry Needling on the Pelvitrochanteric Musculature on the Potential Contraction of the Gluteus Medius in Patients with Greater Trochanteric Pain Syndrome Protocol for a Randomized Clinical Trial Pilot Study
Status:
NOT_YET_RECRUITING
Status Verified Date:
2024-08
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
No
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief 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
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
Detailed Description:
None
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None