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

An Adaptive Psychological Intervention to Improve Pain and Reduce Opioid Use Following an Injury

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07755527
Acronym
HOPE
Enrollment
10
Registered
2026-08-10
Start date
2026-09-01
Completion date
2027-03-01
Last updated
2026-08-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Opioid Use, Pain

Brief summary

The goal of this project is to refine the adaptive psychological intervention and assess initial feasibility and acceptability. Results will be used to inform a pilot randomized trial.

Interventions

BEHAVIORALPsychological Intervention

Participants will complete a computerized brief intervention (education about long-term opioid use and a mindfulness strategy) followed by four psychotherapy sessions composed of education, mindfulness, and acceptance-based strategies.

Sponsors

Henry Ford Health System
Lead SponsorOTHER
National Institute on Drug Abuse (NIDA)
CollaboratorNIH

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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 30 days or more prior to this hospitalization

Design outcomes

Primary

MeasureTime frameDescription
Acceptability of the interventionPost-intervention (40-day follow-up)Percentage of participants that agreed/strongly agreed with items on the acceptability of intervention measure (AIM), intervention appropriateness measure (IAM), and feasibility of intervention measure (FIM).

Secondary

MeasureTime frameDescription
Treatment adherencePost-intervention (40-day follow-up)Percentage of participants that attended at least 3 of 4 sessions
Study adherencePost-intervention (40-day follow-up)Percentage of participants that completed the post-intervention assessment

Contacts

CONTACTLisa Matero, PhD
LMatero1@hfhs.org313-874-5454

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 11, 2026