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Adjunctive Mindfulness During Opioid Tapering for patientS With Chronic Pain (The AMOS Study)

Not Applicable
Recruiting
Conditions
Low Back Pain
Interventions
Behavioral: Psychoeducation
Registration Number
NCT06268522
Lead Sponsor
Brigham and Women's Hospital
Brief Summary

This study is a Randomized Controlled Trial exploring the effects of a Mindfulness interventions in reducing pain interference and opioid dose in patients with Chronic Low Back Pain. A total of 200 opioid-using patients with chronic pain, male and female participants will be enrolled, with a need for 160 completers. Patient will be randomly assigned into the Mindfulness-Oriented Recovery Enhancement or the Psychoeducation comparison control group.

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
200
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
PsychoeducationPsychoeducation-
Primary Outcome Measures
NameTimeMethod
Pain InterferenceBaseline, 8 weeks, 3 month and 6 month follow up

assessed by the Brief pain interventory

Opioid DoseBaseline, 8 weeks, 3 month and 6 month follow up

assessed through their medical record

Secondary Outcome Measures
NameTimeMethod
Opioid MisuseBaseline, 8 weeks, 3 month and 6 month follow up

assessed by the Current Opioid Misuse Measure (COMM)

Opioid CravingBaseline,8 weeks, 3 month and 6 month follow up

assessed by the single item Opioid Craving

Pain IntensityBaseline, 8 weeks, 3 month and 6 month follow up

assessed through the Brief Pain Inventory

Opioid WithdrawalBaseline, 8 weeks, 3 month and 6 month follow up

assessed by the Opioid Withdrawal Scale (SOWS)

Trial Locations

Locations (1)

Brigham and Women's Hospital

🇺🇸

Chestnut Hill, Massachusetts, United States

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