NCT01737073: COMPACT

Comprehensive Opioid Management in Patient Aligned Care Teams

Withdrawn NA Last updated 7 March 2019

What this trial tests

NA trial testing IVR self-management in Chronic Pain. Withdrawn.

Timeline

1 April 2017

Primary endpoint
1 April 2017

1 April 2017

Quick facts

Lead sponsor	VA Office of Research and Development
Phase	NA
Status	Withdrawn
Study type	INTERVENTIONAL
Allocation	randomized
Design	factorial
Masking	single
Primary purpose	treatment
Start date	1 April 2017
Primary completion	1 April 2017
Estimated completion	1 April 2017
Sites	2 locations across United States

Drugs / interventions tested

• IVR self-management
• Opioid monitoring
• Enhanced usual care

Conditions studied

• Chronic Pain — all drugs for Chronic Pain →

Sponsor

VA Office of Research and Development — full company profile →

Who can join

18 and older, any sex, with Chronic Pain. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study will enroll Veterans with chronic pain who have been receiving opioid medications (like methadone, percocet, oxycontin) on a regular basis for at least 3 months to treat their pain. The purpose of this study is to understand if two automated interventions that are delivered by phone can improve the safe and effective use of opioid medications and the physical functioning of Veterans with chronic pain who take opioid medications. One intervention, opioid monitoring, will include monthly automated calls to the enrolled Veteran to ask questions about their use of the opioid medications, pain relief, side effects, effect of pain on physical activity and mood and satisfaction with pain care. The other intervention, skills training, includes learning pain management skills using automated calls and a self-help book with weekly feedback calls from a nurse. Veterans who are enrolled in this study will be randomly assigned (by chance, like a flip of a coin) to receive either opioid monitoring only, self-management only, self-management plus opioid monitoring or a weekly automated phone call with wellness tips. Everyone enrolled in the study will complete questionnaires about their pain and other pain-related information at the beginning of the trial, after the interventions are completed 12 weeks later, and 3 and 6 months after treatment ends.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

1. Automated telephone communication systems for preventive healthcare and management of long-term conditions.
   Posadzki P, Mastellos N, Ryan R, Gunn LH, et al · · 2016 · cited 85× · PMID 27960229 · DOI 10.1002/14651858.cd009921.pub2