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Mindful Moms in Recovery (MMORE)

Primary Purpose

Opioid-use Disorder

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Mindful Moms Yoga Mindfulness Intervention
Sponsored by
Dartmouth-Hitchcock Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Opioid-use Disorder focused on measuring Pregnancy, Mindfulness, Yoga, Substance Use Disorder

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • 18 years of age or older.
  • English-speaking.
  • Singleton pregnancy.
  • Receiving comprehensive medication treatment for opioid use disorder as part of prenatal care at a partner maternity care practice.

Exclusion Criteria:

  • Cognitive or psychiatric impairments that prohibit being able to provide informed consent.
  • Any physical conditions that prohibit activity such as gentle yoga.

Sites / Locations

  • Dartmouth Hitchcock Medical CenterRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Intervention as adjunct to Treatment as Usual

Treatment as Usual

Arm Description

Participants will attend an 8-session group-based yoga-mindfulness intervention offered over the course of approximately 10 consecutive weeks. Participants will also be asked to use a mobile companion app once a week during the intervention period. All intervention participants also receive treatment as usual for OUD at the partner practice, which includes medication for OUD, individual and/or group counseling, and case management.

Participants receive treatment as usual for OUD at the partner practice, which includes medication for OUD, individual and/or group counseling, and case management.

Outcomes

Primary Outcome Measures

Retention in medication treatment for opioid use disorder as assessed by number of weeks buprenorphine or methadone present in urine toxicology screening in clinical record conducted as part of treatment as usual.
Data collected through review of clinical record review of consented participants.
Change in opioid abstinence from baseline as assessed by number of weeks consistently abstinent from opioids as determined by weekly point of care urine toxicology screening conducted as part of treatment as usual.
Data collected through review of clinical record of consented participants.

Secondary Outcome Measures

Change in opioid and other substance use from baseline, as assessed with the World Health Organization (WHO) Alcohol, Smoking and Substance Involvement Screening Test (ASSIST) V3.0.
The Alcohol, Smoking and Substance Involvement Screening Test contains 7 questions and asks about past and current substance use and addiction to various substances. Each substance ranges in scores between 0 to 27+ with higher scores indicating greater risk level of addiction and dependence. Opioid addiction severity will be measured by 11 "yes or no" response items aligned with the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-V) criteria with more "yes" responses indicating higher opioid addiction severity.
Change in depression from baseline, as assessed with the Edinburgh Prenatal and Postnatal Depression Scale.
The Edinburgh Prenatal and Postnatal Depression Scale contains 10 questions with scores ranging from 10 to 40 with higher scores indicating greater depression symptoms.
Change in anxiety from baseline, as assessed with the Generalized Anxiety Disorder Scale (GAD)
The Generalized Anxiety Disorder Scale contains 7 questions with scores ranging from 0 to 21, with higher scores indicating greater anxiety symptoms.
Change in stress from baseline, as assessed with the Perceived Stress Scale
The Perceived Stress Scale contains 10 questions with scores ranging from 0 to 40 with higher scores indicating greater stress.
Change in post-traumatic stress from baseline, as assessed with the abbreviated Post-Traumatic Stress Disorder (PTSD) Checklist screening instrument.
The abbreviated Post-Traumatic Stress Disorder Checklist screening instrument contains 20 questions with scores ranging from 0 to 80 with higher scores indicating greater PTSD symptoms.
Change in mindfulness from baseline, as assessed with the Mindful Attention Awareness Scale (MAAS)
The Mindful Attention Awareness Scale contains 15 questions with scores ranging between 1 and 6 with higher scores indicating greater mindfulness.

Full Information

First Posted
October 6, 2020
Last Updated
October 3, 2022
Sponsor
Dartmouth-Hitchcock Medical Center
Collaborators
National Center for Complementary and Integrative Health (NCCIH), Trustees of Dartmouth College
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1. Study Identification

Unique Protocol Identification Number
NCT04584502
Brief Title
Mindful Moms in Recovery
Acronym
MMORE
Official Title
Mindful Moms in Recovery: Yoga-based Mindfulness Relapse Prevention for Pregnant Women With Opioid Use Disorder
Study Type
Interventional

2. Study Status

Record Verification Date
October 2022
Overall Recruitment Status
Recruiting
Study Start Date
May 1, 2022 (Actual)
Primary Completion Date
July 31, 2023 (Anticipated)
Study Completion Date
September 30, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Dartmouth-Hitchcock Medical Center
Collaborators
National Center for Complementary and Integrative Health (NCCIH), Trustees of Dartmouth College

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to evaluate the initial efficacy of a yoga-mindfulness intervention to promote ongoing recovery for pregnant and parenting women with Opioid Use Disorder (OUD) receiving perinatal services and medication treatment for OUD from maternity care practices in New Hampshire.
Detailed Description
In this R33 project, the study team will conduct a randomized controlled trial to evaluate the efficacy and implementation of the Mindful Moms intervention (MMORE) with a group of pregnant women with identified OUD receiving medication treatment for OUD at partner maternity care practices. The study team will evaluate the impact of Mindful Moms as an adjunct to treatment as usual on retention in medication for opioid use disorder (MOUD) treatment, substance use, and relapse-related risks. This study has three Specific Aims: Aim 1: Evaluate MMORE in a randomized controlled study with pregnant women as an adjunct to MOUD treatment as usual care for impact on treatment retention, opioid abstinence, and relapse risks. Aim 2: Examine mechanisms of effect of MMORE on outcomes. Aim 3: Evaluate barriers and facilitators to sustainable implementation of MMORE as an adjunct to MOUD for pregnant and parenting women.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Opioid-use Disorder
Keywords
Pregnancy, Mindfulness, Yoga, Substance Use Disorder

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Intervention as adjunct to usual care.
Masking
InvestigatorOutcomes Assessor
Masking Description
The study will be blind to the Principal Investigators, the statistician, and to those on the team responsible for participant data collection. The study team will work to try to blind clinicians delivering treatment as usual to participant assignment but there is a chance that patients will reveal their condition to clinicians despite our best efforts. To achieve blindness, treatment assignment will done by the Project Manager, who will not be directly involved in evaluation data collection. Data collection will be conducted by the study Research Assistant who will be blinded to participant treatment assignment.
Allocation
Randomized
Enrollment
120 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Intervention as adjunct to Treatment as Usual
Arm Type
Experimental
Arm Description
Participants will attend an 8-session group-based yoga-mindfulness intervention offered over the course of approximately 10 consecutive weeks. Participants will also be asked to use a mobile companion app once a week during the intervention period. All intervention participants also receive treatment as usual for OUD at the partner practice, which includes medication for OUD, individual and/or group counseling, and case management.
Arm Title
Treatment as Usual
Arm Type
No Intervention
Arm Description
Participants receive treatment as usual for OUD at the partner practice, which includes medication for OUD, individual and/or group counseling, and case management.
Intervention Type
Behavioral
Intervention Name(s)
Mindful Moms Yoga Mindfulness Intervention
Other Intervention Name(s)
MMORE
Intervention Description
MMORE is an 8-session yoga-mindfulness intervention protocol, offered over the course of 10 consecutive weeks at the partner maternity care practice or a nearby location. Each session will last approximately 60 minutes (8 - 10 participants per group). Intervention participants will also be asked to use a mobile companion app at least once each week of the intervention period.
Primary Outcome Measure Information:
Title
Retention in medication treatment for opioid use disorder as assessed by number of weeks buprenorphine or methadone present in urine toxicology screening in clinical record conducted as part of treatment as usual.
Description
Data collected through review of clinical record review of consented participants.
Time Frame
baseline to 3-months postpartum
Title
Change in opioid abstinence from baseline as assessed by number of weeks consistently abstinent from opioids as determined by weekly point of care urine toxicology screening conducted as part of treatment as usual.
Description
Data collected through review of clinical record of consented participants.
Time Frame
baseline to 3-months postpartum
Secondary Outcome Measure Information:
Title
Change in opioid and other substance use from baseline, as assessed with the World Health Organization (WHO) Alcohol, Smoking and Substance Involvement Screening Test (ASSIST) V3.0.
Description
The Alcohol, Smoking and Substance Involvement Screening Test contains 7 questions and asks about past and current substance use and addiction to various substances. Each substance ranges in scores between 0 to 27+ with higher scores indicating greater risk level of addiction and dependence. Opioid addiction severity will be measured by 11 "yes or no" response items aligned with the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-V) criteria with more "yes" responses indicating higher opioid addiction severity.
Time Frame
Baseline, 8 weeks, and 3-months postpartum
Title
Change in depression from baseline, as assessed with the Edinburgh Prenatal and Postnatal Depression Scale.
Description
The Edinburgh Prenatal and Postnatal Depression Scale contains 10 questions with scores ranging from 10 to 40 with higher scores indicating greater depression symptoms.
Time Frame
Baseline, 8 weeks, and 3-months postpartum
Title
Change in anxiety from baseline, as assessed with the Generalized Anxiety Disorder Scale (GAD)
Description
The Generalized Anxiety Disorder Scale contains 7 questions with scores ranging from 0 to 21, with higher scores indicating greater anxiety symptoms.
Time Frame
Baseline, 8 weeks, and 3-months postpartum
Title
Change in stress from baseline, as assessed with the Perceived Stress Scale
Description
The Perceived Stress Scale contains 10 questions with scores ranging from 0 to 40 with higher scores indicating greater stress.
Time Frame
Baseline, 8 weeks, and 3-months postpartum
Title
Change in post-traumatic stress from baseline, as assessed with the abbreviated Post-Traumatic Stress Disorder (PTSD) Checklist screening instrument.
Description
The abbreviated Post-Traumatic Stress Disorder Checklist screening instrument contains 20 questions with scores ranging from 0 to 80 with higher scores indicating greater PTSD symptoms.
Time Frame
Baseline, 8 weeks, and 3-months postpartum
Title
Change in mindfulness from baseline, as assessed with the Mindful Attention Awareness Scale (MAAS)
Description
The Mindful Attention Awareness Scale contains 15 questions with scores ranging between 1 and 6 with higher scores indicating greater mindfulness.
Time Frame
Baseline, 8 weeks, and 3-months postpartum
Other Pre-specified Outcome Measures:
Title
Change in pain perception from baseline, as measured by the visual analog scale (VAS)
Description
The Visual Analog Scale is a scale ranging from 0 (no pain) to 10 (worst possible pain) and anchored with descriptive faces.
Time Frame
Baseline, 8 weeks, and 3-months postpartum
Title
Change from baseline in quality of life measured by the World Health Organization (WHO) Quality of Life Brief.
Description
The World Health Organization Quality of Life - Brief instrument contains 26 questions to assess a quality of life profile based on four domains: physical health, psychological health, social relationships, and environment. Each domain ranges in score from 0 to 100 where higher scores denote higher quality of life.
Time Frame
Baseline, 8 weeks, and 3-months postpartum

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 18 years of age or older. English-speaking. Singleton pregnancy. Receiving comprehensive medication treatment for opioid use disorder as part of prenatal care at a partner maternity care practice. Exclusion Criteria: Cognitive or psychiatric impairments that prohibit being able to provide informed consent. Any physical conditions that prohibit activity such as gentle yoga.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Sarah E Lord, PhD
Phone
603-646-7089
Email
sarah.e.lord@dartmouth.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sarah E Lord, PhD
Organizational Affiliation
Geisel School of Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
Dartmouth Hitchcock Medical Center
City
Lebanon
State/Province
New Hampshire
ZIP/Postal Code
03766
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Sarah Lord, Ph.D.

12. IPD Sharing Statement

Learn more about this trial

Mindful Moms in Recovery

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