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

ConditionsPainOpioid Use
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorHenry Ford Health System

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Admitted to Henry Ford Hospital

Has an acute musculoskeletal injury

Prescribed opioids during the admission

Disqualifiers

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

Trial design

Design model

Single group

Treatments tested in this trial

  • Psychological Intervention

    Behavioral

    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.

Treatment groups

10 Participants
are divided into 1 treatment group
Group A: Psychological InterventionExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Acceptability of the intervention

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).

Time frame
Post-intervention (40-day follow-up)

Secondary outcomes

1

Treatment adherence

Percentage of participants that attended at least 3 of 4 sessions

Time frame
Post-intervention (40-day follow-up)
2

Study adherence

Percentage of participants that completed the post-intervention assessment

Time frame
Post-intervention (40-day follow-up)

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Henry Ford Health System

Lead sponsor

National Institute on Drug Abuse (NIDA)

Collaborator

Source ClinicalTrials.gov

This trial is not recruiting at the moment. You can still explore other options: