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Mindfulness-Based Intervention for Opioid Use Disorder
N/A
Waitlist Available
Led By Cynthia Price, PhD
Research Sponsored by University of Washington
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 90 days
Awards & highlights
Summary
This trial will test if a mindfulness-based intervention can help people with opioid use disorder who are receiving medication treatment to reduce opioid use and improve mental and physical health.
Who is the study for?
This trial is for individuals enrolled in a medication treatment program for opioid use disorder who are stable on their current regimen, fluent in English, and willing to commit to the study's requirements. Pregnant women over 24 weeks gestation or with unknown gestation, those showing psychosis or cognitive impairment, or unable to remain in treatment for the trial duration are excluded.Check my eligibility
What is being tested?
The study tests Mindful Awareness in Body-oriented Therapy (MABT) as an add-on to standard Medication for Opioid Use Disorder (MOUD). Participants will be randomly assigned to receive either MABT+MOUD or MOUD alone and will be evaluated over time to see which group fares better regarding opioid use, mental and physical health, cravings, and treatment retention.See study design
What are the potential side effects?
Since MABT is a mindfulness-based intervention focusing on body awareness without medication changes, significant side effects aren't anticipated. However, participants may experience emotional discomfort when engaging with mindfulness practices that encourage increased awareness of bodily sensations.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 90 days
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~90 days
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Time Line Follow-back
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: MABT* + Medication TreatmentExperimental Treatment1 Intervention
Mindful Awareness in Body-oriented Therapy + Medication Treatment
Group II: Treatment as UsualActive Control1 Intervention
Treatment as Usual is medication for the treatment of opioid use disorder
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Mindful Awareness in Body-oriented Therapy
2019
Completed Phase 1
~570
Find a Location
Who is running the clinical trial?
University of WashingtonLead Sponsor
1,762 Previous Clinical Trials
1,876,179 Total Patients Enrolled
National Center for Complementary and Integrative Health (NCCIH)NIH
837 Previous Clinical Trials
670,079 Total Patients Enrolled
Cynthia Price, PhD4.840 ReviewsPrincipal Investigator - University of Washington
Medical School - University of Arizona
University of California, Los Angeles, Residency in Pediatrics
2 Previous Clinical Trials
45 Total Patients Enrolled
2Patient Review
I felt like she was rushing me through the appointment. I was in and out in less than 10 minutes and it cost me $45.
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Eligibility Criteria:
This trial includes the following eligibility criteria:- You agree to stop receiving non-study manual therapies (like massages) and mind-body therapies (like meditation) for 3 months.You have a mental illness, such as severe confusion or hallucinations, that would interfere with the study.You have been diagnosed with addiction to opioid drugs.
Research Study Groups:
This trial has the following groups:- Group 1: MABT* + Medication Treatment
- Group 2: Treatment as Usual
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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