Ignite Creation Date:
2024-10-26 @ 3:37 PM
Last Modification Date:
2024-10-26 @ 3:37 PM
Study NCT ID:
NCT06540911
Status:
NOT_YET_RECRUITING
Last Update Posted:
None
First Post:
2024-07-19
Brief Title:
Personalized Physical Back Training Program to Improve Physical Functioning in People With Non-specific Low Back Pain A Feasibility Study
Sponsor:
None
Organization:
None
Study Overview
Official Title:
Personalized Physical Back Training Program to Improve Physical Functioning in People With Non-specific Low Back Pain A Feasibility 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:
LIFDI
Brief Summary:
The aim of our clinical trial 2024-01285 is to determine how an individualized physical back training program affects physical functioning and back pain The results will help identify the most effective treatments for low back pain This feasibility study 2024-01284 aims to conduct a test run of the clinical trial The main questions are
Do all procedures run smoothly
Does the back training program improve physical functioning
Does the back training program reduce back pain
Participants will
Follow a back training program for 4 weeks
Attend group exercise sessions 30 minutes per week
Perform exercises at home 3x10 minutes per week
Fill out a daily questionnaire on pain and exercise adherence
Do all procedures run smoothly
Does the back training program improve physical functioning
Does the back training program reduce back pain
Participants will
Follow a back training program for 4 weeks
Attend group exercise sessions 30 minutes per week
Perform exercises at home 3x10 minutes per week
Fill out a daily questionnaire on pain and exercise adherence
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