Ignite Creation Date:
2024-05-19 @ 5:34 PM
Last Modification Date:
2024-10-26 @ 3:29 PM
Study NCT ID:
NCT06418217
Status:
RECRUITING
Last Update Posted:
2024-05-23
First Post:
2024-05-13
Brief Title:
Exercise and Patient Education for Patients With Lateral Hip Pain
Sponsor:
Jeppe Lange
Organization:
Horsens Hospital
Study Overview
Official Title:
3 Months Semi-supervised Exercise Intervention for Patients With Hip Abductor Tendon Pathology HATP A Prospective Clinical Cohort Study
Status:
RECRUITING
Status Verified Date:
2024-05
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
This prospective cohort trial will investigate a progressive exercise protocol and patient education for patients with hip abductor tendon pathology The primary outcome is patient reported pain measured by the revised Copenhagen Hip And Groin Outcome Score HAGOS that will be conducted at baseline and at a 12 week follow-up
Detailed Description:
This study protocol describes an interventional pragmatic prospective single-group cohort study where the primary endpoint is change in hip pain measured with the revised HAGOS pain subscale following a 12 week intervention Throughout the 12 weeks eight physiotherapist-led exercise sessions will take place at Horsens Regional Hospital HRH Further at the sessions at HRH patient education will be performed by the supervising physiotherapist The first supervised sessions will be performed in continuation of the baseline assessment The patients will be instructed to do the exercises daily at home in the time period between the physiotherapist-led sessions
The primary aim is to investigate changes in patient-reported hip pain based on the subscale pain from the revised Copenhagen Hip And Groin Outcome Score HAGOS from baseline to 12 week follow-up
It is hypothesized that the revised HAGOS pain score will improve from baseline to 12 week follow-up
Secondarily explorative subgroup analyses regarding whether patients with different MRI findings pain profiles age sex and body mass index BMI respond differently to the intervention will be performed
All outcomes conducted will be published That is patient-reported outcomes muscle strength functional capacity and adherence to the exercise protocol
A full study protocol will be published and made available
The primary aim is to investigate changes in patient-reported hip pain based on the subscale pain from the revised Copenhagen Hip And Groin Outcome Score HAGOS from baseline to 12 week follow-up
It is hypothesized that the revised HAGOS pain score will improve from baseline to 12 week follow-up
Secondarily explorative subgroup analyses regarding whether patients with different MRI findings pain profiles age sex and body mass index BMI respond differently to the intervention will be performed
All outcomes conducted will be published That is patient-reported outcomes muscle strength functional capacity and adherence to the exercise protocol
A full study protocol will be published and made available
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None