Healing After Injury to Reduce Opioid Use and Pain Through Preventive Engagement

Sponsor
Henry Ford Health System
Study ID
NCT07741201
Status
Not Yet Recruiting

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Conditions

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • Computerized brief intervention — BEHAVIORAL
    Education about long-term opioid use and a mindfulness strategy
  • Psychological sessions — BEHAVIORAL
    Four sessions composed of education, mindfulness, and acceptance-based strategies.
  • Opioid taper recommendations — BEHAVIORAL
    Recommendations will be provided to taper opioid use.

Study Details

The goal of this proposed project is to optimize the adaptive psychological intervention and assess the feasibility and acceptability. The long-term objective of this line of research is to evaluate whether an adaptive psychological intervention delivered after a musculoskeletal injury is effective in preventing the development of chronic pain and long-term opioid use.

Key Dates

First listed
Aug 3, 2026
Start date
Mar 1, 2027
Status verified
Aug 2026
Primary completion
May 31, 2028
Completion
May 31, 2028

Study Design

Enrollment
80 participants (estimated)
Allocation
RANDOMIZED
Intervention model
SEQUENTIAL
Primary purpose
PREVENTION

Arms

  • No Intervention: Subgroup 1
    Participants who were not randomized to the computerized brief intervention and were no longer on opioids 10 days post-baseline and did not receive any further treatment.
  • Active Comparator: Subgroup 2
    Participants who were not randomized to the computerized brief intervention but were on opioids 10 days post-baseline and received recommendations for an opioid taper.
  • Experimental: Subgroup 3
    Participants who were randomized to the computerized brief intervention but were no longer on opioids 10 days post-baseline and did not receive any further treatment.
  • Experimental: Subgroup 4
    Participants who were randomized to the computerized brief intervention and were still on opioids 10 days post-baseline and were then randomized to receive the recommendations for the opioid taper.
  • Experimental: Subgroup 5
    Participants who were randomized to the computerized brief intervention and were still on opioids 10 days post-baseline and were then randomized to receive the recommendations for the opioid taper plus additional psychological treatment sessions.

Primary Outcome Measure

Opioid use [ Time Frame: 90-day follow-up ]

Central Contacts

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