COMmunity of Practice And Safety Support for Navigating Pain (COMPASS-NP)
COMPASS-NP
Translating an Intervention to Address Chronic Pain Among Home Care Workers
1 other identifier
interventional
140
1 country
1
Brief Summary
Home care workers (HCWs) are at-risk for chronic pain and associated problems, including emotional distress, opioid use and misuse, and work-related disability. To address these issues, the proposed study will adapt an established peer-led and supportive group program to address the needs of HCWs with chronic pain. The new program, named COMPASS for Navigating Pain (COMPASS-NP), will integrate work-based injury protections with pain education and cognitive-behavioral therapy strategies for pain self-management in order to reduce pain interference with HCWs' work and life, and advance their safety, health, and well-being.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Aug 2023
Typical duration for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
February 18, 2022
CompletedFirst Posted
Study publicly available on registry
August 9, 2022
CompletedStudy Start
First participant enrolled
August 21, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 11, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
September 1, 2026
ExpectedNovember 28, 2025
November 1, 2025
1.6 years
February 18, 2022
November 21, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Between Groups Difference in Changes in Ratings of Pain Interference with Work
Work Limitations Questionnaire (1-5; 5=worst \[limited all the time\]). Assesses limitations related to time, physical, mental-interpersonal, and outputs.
Changes between 0 weeks and 10 weeks
Between Groups Difference in Changes in Ratings of Pain Interference with Life
Brief Pain Inventory Subscale on pain interference (0-10; 10=worst \[completely interferes\]). Interference related to general activity, walking, work, relations with other people, sleep, and enjoyment of life.
Changes between 0 weeks and 10 weeks
Secondary Outcomes (11)
Between Groups Difference in Changes in Reported Number of Pain/Injury Prevention Actions
Changes between 0 weeks and 10 weeks
Between Groups Difference in Changes in Reported Number of Minor Injuries
Changes between 0 weeks and 10 weeks
Between Groups Difference in Changes in Reported Number of Lost Work Time Injuries
Changes between 0 weeks and 10 weeks
Between Groups Difference in Changes in the Rating of Average Pain Severity
Changes between 0 weeks and 10 weeks
Between Groups Difference in Changes in Ratings of Well-being
Changes between 0 weeks and 10 weeks
- +6 more secondary outcomes
Study Arms (2)
Intervention
EXPERIMENTALIntervention during weeks 0-10 (10 weekly group sessions). Follow-up with no treatment during weeks 11-20.
Waitlist Control
OTHERUsual practice during weeks 0-10. Intervention during weeks 11-20 (10 weekly group sessions).
Interventions
A peer-led and supportive group program (10 weekly sessions) designed to address the needs of HCWs with chronic or elevated pain. The intervention will integrate work-based injury protections with pain education and cognitive-behavioral therapy strategies for pain self-management.
Eligibility Criteria
You may qualify if:
- years (adults)
- Employed as a home care worker
- Has chronic pain (pain lasting 3+ months and \> 4 average intensity)
- The presence of pain interference with work (response of 'agree' or 'strongly agree' on single-item)
- Currently working 4 hours or more per week
- Access to the internet with a video capable device (e.g., smart phone, tablet, or computer)
You may not qualify if:
- Prior exposure to the original COMPASS program
- Experiencing a surgery in the prior 6 months
- Current pregnancy or intention to become pregnant during the study period.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Oregon Health & Science University
Portland, Oregon, 97239, United States
Related Publications (1)
Olson R, Hess JA, Turk D, Marino M, Greenspan L, Alley L, Donovan C, Rice SPM. COMMunity of Practice And Safety Support for Navigating Pain (COMPASS-NP): study protocol for a randomized controlled trial with home care workers. Trials. 2023 Apr 10;24(1):264. doi: 10.1186/s13063-023-07149-8.
PMID: 37038235DERIVED
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- PREVENTION
- Intervention Model
- CROSSOVER
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
February 18, 2022
First Posted
August 9, 2022
Study Start
August 21, 2023
Primary Completion
April 11, 2025
Study Completion (Estimated)
September 1, 2026
Last Updated
November 28, 2025
Record last verified: 2025-11