Ignite Creation Date:
2024-05-06 @ 8:26 PM
Last Modification Date:
2024-10-26 @ 3:28 PM
Study NCT ID:
NCT06387563
Status:
RECRUITING
Last Update Posted:
2024-04-29
First Post:
2024-04-23
Brief Title:
Effects of Abdominal Muscle Activation Training Using Pressure Biofeedback in Comparison With Surface Electromyography
Sponsor:
Foundation University Islamabad
Organization:
Foundation University Islamabad
Study Overview
Official Title:
Effects of Abdominal Muscle Activation Training Using Pressure Biofeedback in Comparison With Surface Electromyography
Status:
RECRUITING
Status Verified Date:
2024-04
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 study is a randomized control trial and the purpose of this study to determine the effects of abdominal muscle activation training on non-specific low back pain using pressure biofeedback in comparison with surface electromyography biofeedback a randomized control trial
Detailed Description:
The purpose of this study is to determine the effects of abdominal muscle activation training using pressure biofeedback in comparison with surface electromyography biofeedback in management of non-specific low back pain a randomized control trial
Pain and disability are the primary outcomes which will be determined using
1 Numeric pain rating scale NPRS
2 Oswestry disability index ODI Data will be taken before and after the intervention protocol for each participant
Data collection procedure Participants of interest would be approached and explained about the research Informed written consent will be taken Pre and post intervention scores will be recorded
Pain and disability are the primary outcomes which will be determined using
1 Numeric pain rating scale NPRS
2 Oswestry disability index ODI Data will be taken before and after the intervention protocol for each participant
Data collection procedure Participants of interest would be approached and explained about the research Informed written consent will be taken Pre and post intervention scores will be recorded
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