Ignite Creation Date:
2024-05-06 @ 1:03 PM
Last Modification Date:
2024-10-26 @ 1:08 PM
Study NCT ID:
NCT03925077
Status:
RECRUITING
Last Update Posted:
2023-08-29
First Post:
2019-03-27
Brief Title:
Spinal Cord Injury Program in Exercise
Sponsor:
University of Alabama at Birmingham
Organization:
University of Alabama at Birmingham
Study Overview
Official Title:
RERC on Technologies to Promote Exercise and Health Among People With Disabilities A Scale Up Study Evaluating a Movement-to-Music Teleexercise Platform for Reaching a National Cohort of People With Spinal Cord Injury
Status:
RECRUITING
Status Verified Date:
2024-08
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:
SCIPE
Brief Summary:
The purpose of this study is to examine two 8-week remotely delivered exercise interventions Movement-to-Music M2M and Standard Exercise Training SET with 327 adults with spinal cord injury Enrolled participants will be randomized into one of three groups a M2M b SET and c attention control AC
Detailed Description:
The purpose of the Spinal Cord Injury Program in Exercise SCIPE study is to examine two 8-week remotely delivered exercise interventions Movement-to-Music M2M and Standard Exercise Training SET with 327 adults with SCI The primary aim is to examine change in physical activity level after the 8-week M2M and SET interventions We hypothesize that participants in M2M and SET will have significant increase in physical activity compared to an Attention Control AC group after the 8-week intervention The secondary aim is to examine effects of the M2M and SET interventions on health and quality of life outcomes We hypothesize that participants in M2M and SET will have significant increases in sleep quality and quality of life and decreases in pain and fatigue compared to AC after the 8-week intervention Exercise enjoyment in M2M and SET participants will also be explored The tertiary aim is to evaluate the demographic age race sex clinical level of injury type of injury and psychosocial social support outcome expectations self-efficacy self-regulation variables of two participant groups 1 compliant participants who completed 50 of the intervention and 2 noncompliant participants who completed post-testing but 50 of the intervention or who did not complete post-testing
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