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Problem-solving Pain to Enhance Living Well (PROPEL) for Self-Management (PROPEL Trial)
N/A
Waitlist Available
Led By Kyounghae Kim, PhD
Research Sponsored by University of Connecticut
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline, 2, 4, 6, 8, 10 and 12 weeks
Awards & highlights
PROPEL Trial Summary
This study is evaluating whether a self-management program can help individuals with chronic low back pain.
Eligible Conditions
- Chronic Lower Back Pain
- Self-Management
PROPEL Trial Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ baseline, 2, 4, 6, 8, 10 and 12 weeks
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline, 2, 4, 6, 8, 10 and 12 weeks
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Change in physical activity
Secondary outcome measures
Change in gene expression profiles
Change in pain sensitivity
Relationship between pain self-management and pain interferance
+2 morePROPEL Trial Design
1Treatment groups
Experimental Treatment
Group I: PROPELExperimental Treatment1 Intervention
The Problem-solving Pain to Enhance Living Well (PROPEL) intervention entails each participant watching 10 video modules via REDCap. These modules include: (1) pain neurophysiology, (2) catastrophizing, (3) stress reactivity, (4) fear of movement, (5) progressive relaxation, (6) deep breathing, (7) guided imagery, (8) heat, ice and stretching, (9) strategies for physical activity self-activation and (10) problem-solving.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Problem-solving Pain to Enhance Living Well (PROPEL)
2018
N/A
~40
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Who is running the clinical trial?
University of ConnecticutLead Sponsor
183 Previous Clinical Trials
158,133 Total Patients Enrolled
National Institute of Nursing Research (NINR)NIH
580 Previous Clinical Trials
10,376,524 Total Patients Enrolled
Kyounghae Kim, PhDPrincipal InvestigatorUniversity of Connecticut
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