Healing After Injury to Reduce Opioid Use and Pain Through Preventive Engagement | NCT07741201

NCT07741201

Overview

NCT ID: NCT07741201
Lead Sponsor: Henry Ford Health SystemOTHER
Official Title: An Adaptive Psychological Intervention to Improve Pain and Reduce Opioid Use Following an Injury
Brief Summary: 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.
Conditions: Pain
Opioid Use
Interventions

Status and Timeline

Status: Not yet recruiting
Last Update Posted: Aug 3, 2026Actual
Start Date: Oct 1, 2026Estimated
Primary Completion Date: May 31, 2028Estimated
Completion Date

Participation Criteria

Ages Eligible for Study: Adult (18-64)Older Adult (65+)
Sexes Eligible for Study: All
Accepts Healthy Volunteers?: No
Eligibility Criteria: Inclusion Criteria:

Admitted to Henry Ford Hospital

Has an acute musculoskeletal injury

Prescribed opioids during the admission

Exclusion Criteria:

Under age 18

Cognitive impairment (i.e., diagnosis of delirium, dementia, or traumatic brain injury/Glasgow Coma Scale less than 13)

Chronic pain condition (i.e., pain most of the day, nearly every day for the past 3 months or longer)

Taking opioids within the 30 days prior to this hospitalization

Study Plan

Study Type: Interventional
Phase: Not Applicable
Enrollment: 80Estimated
Primary Purpose: Prevention
Allocation: Randomized
Interventional Model: Sequential Assignment
Masking: None (Open Label)

Contacts and Locations

Central Contacts: Lisa Matero, PhDContact
LMatero1@hfhs.org313-874-5454

Similar Studies

Participant Group/Arms

Subgroup 1No Intervention

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.

Subgroup 2Active Comparator

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.

Behavioral: Opioid taper recommendations

Subgroup 3Experimental

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.

Behavioral: Computerized brief intervention

Subgroup 4Experimental

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.

Behavioral: Computerized brief intervention

Subgroup 5Experimental

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.

Behavioral: Computerized brief intervention