Ignite Creation Date:
2024-07-17 @ 10:55 AM
Last Modification Date:
2024-10-26 @ 3:34 PM
Study NCT ID:
NCT06492642
Status:
RECRUITING
Last Update Posted:
2024-07-09
First Post:
2024-06-21
Brief Title:
Research Study on Patient Education for People With Chronic Low Back Pain
Sponsor:
University of Pittsburgh
Organization:
University of Pittsburgh
Study Overview
Official Title:
Pilot Study of Personalized Patient Education for Chronic Low Back Pain
Status:
RECRUITING
Status Verified Date:
2024-09
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:
The goal of this pilot single-arm study is to examine the potential of personalized patient education materials to improve self-efficacy and perceived functional disability in patients with chronic low back pain The main questions it aims to answer are
1 What is the feasibility of delivering a personalized patient education program for individuals with chronic low back pain
2 What is the impact of personalized patient education materials on disease-specific self-efficacy and patient-reported function in a small sample of individuals with chronic low back pain
Participants will be asked to
access and complete online baseline questionnaires
access and follow online patient materials on chronic low back pain on days 5 8 11 14 and 17
access and complete online follow-up responses to baseline questionnaires and a post-study survey
1 What is the feasibility of delivering a personalized patient education program for individuals with chronic low back pain
2 What is the impact of personalized patient education materials on disease-specific self-efficacy and patient-reported function in a small sample of individuals with chronic low back pain
Participants will be asked to
access and complete online baseline questionnaires
access and follow online patient materials on chronic low back pain on days 5 8 11 14 and 17
access and complete online follow-up responses to baseline questionnaires and a post-study survey
Detailed Description:
This is a pilot single-arm study to examine the potential of personalized patient education materials to improve self-efficacy and perceived functional disability for patients with chronic low back pain cLBP
The investigators aim to recruit 30 individuals with cLBP The investigators will aim to recruit 15 individuals from areas with an Area Deprivation Index ADI of at least 6 and 15 from areas with an ADI of 5 or lower
Participants will complete a 3-week educational intervention aimed at improving self-efficacy in managing chronic LBP Educational materials will be personalized for each participant depending upon things like baseline knowledge of cLBP smoking status exercise status beliefs about safe movement with cLBP preference for various health care interventions and nature of work sedentary vs labor-oriented job
Educational materials will be provided electronically using Qualtrics
Participants will complete outcome measures at baseline and follow-up as described elsewhere in this study record
The investigators aim to recruit 30 individuals with cLBP The investigators will aim to recruit 15 individuals from areas with an Area Deprivation Index ADI of at least 6 and 15 from areas with an ADI of 5 or lower
Participants will complete a 3-week educational intervention aimed at improving self-efficacy in managing chronic LBP Educational materials will be personalized for each participant depending upon things like baseline knowledge of cLBP smoking status exercise status beliefs about safe movement with cLBP preference for various health care interventions and nature of work sedentary vs labor-oriented job
Educational materials will be provided electronically using Qualtrics
Participants will complete outcome measures at baseline and follow-up as described elsewhere in this study record
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