Ignite Creation Date:
2024-10-26 @ 3:39 PM
Last Modification Date:
2024-10-26 @ 3:39 PM
Study NCT ID:
NCT06587399
Status:
NOT_YET_RECRUITING
Last Update Posted:
None
First Post:
2024-09-04
Brief Title:
Comparison of Manual Therapy Versus Radial Shock Waves in the Shoulder Pain Treatment
Sponsor:
None
Organization:
None
Study Overview
Official Title:
Comparison of Manual Therapy Versus Low-medium Energy Radial Shock Waves in the Treatment of Subacromial Syndrome in a Randomized Clinical Trial
Status:
NOT_YET_RECRUITING
Status Verified Date:
2024-09
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:
Subacromial syndrome represents the third leading cause of pain in the general population There is no clear pathophysiological explanation nor a specific treatment Manual therapy stands out as one of the reference treatments for this disease however it is complex to develop a specific protocol On the other hand shock waves have still not received adequate attention in the treatment of this pathology The aim of this study will focus on using manual treatment using ischemic pressure joint mobilizations and myofascial techniques in comparison to shock wave therapy to determine which is more effective
This study will be a randomized single-blind clinical trial with third-party evaluation In it 88 subjects suffering from subacromial syndrome will participate 44 patients will receive treatment through manual therapy over 6 weeks and other 44 patients through low-med energy radial shock waves for 6 weeks
All subjects will complete their treatment with a 12-week home-based therapeutic exercise program
The main endpoint of the study will be pain measured using the visual analogue scale VAS in motion Pain will also be assessed using the VAS scale at rest and overnight The Spadi Spanish version questionnaire will be used shoulder strength will be measured using a handheld dynamometer and the ranges of motion will be measured
Data will be measured before and one year after treatment
This study will be a randomized single-blind clinical trial with third-party evaluation In it 88 subjects suffering from subacromial syndrome will participate 44 patients will receive treatment through manual therapy over 6 weeks and other 44 patients through low-med energy radial shock waves for 6 weeks
All subjects will complete their treatment with a 12-week home-based therapeutic exercise program
The main endpoint of the study will be pain measured using the visual analogue scale VAS in motion Pain will also be assessed using the VAS scale at rest and overnight The Spadi Spanish version questionnaire will be used shoulder strength will be measured using a handheld dynamometer and the ranges of motion will be measured
Data will be measured before and one year after treatment
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