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A Pilot Feasibility Study of Mindfulness-Oriented Recovery Enhancement With Pregnant Women With Opioid Use Disorder

University of Montana logo

University of Montana

Status

Terminated

Conditions

Opioid-use Disorder

Treatments

Behavioral: Mindfulness-Oriented Recovery Enhancement

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT04824521
5P20GM130418 (U.S. NIH Grant/Contract)
2-21

Details and patient eligibility

About

Thirty pregnant women with substance use disorder will be recruited to participate in eight sessions of MORE.

Full description

Participants will be asked to complete a battery of self-report measures and a semi-structured qualitative interview at three times points-before the intervention begins, after session four, and again after session eight. Participants will also be asked to complete self-report measures before and after each session. The primary aims of this study are as follows.

Aim 1: To adapt the in-person MORE intervention for telehealth delivery. Aim 2: To assess the overall feasibility and acceptability of this telehealth intervention. Hypothesis: MORE delivered via telehealth will be both feasible and acceptable to participants.

Enrollment

1 patient

Sex

Female

Ages

18 to 60 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Must be pregnant.
  • Must be able to communicate in English.
  • Must have met criteria for opioid use disorder in the past year.

Exclusion criteria

  • None.

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

1 participants in 1 patient group

Mindfulness-Oriented Recovery Enhancement via tele-health
Experimental group
Description:
Participants will be assigned to 8 weeks of Mindfulness-Oriented Recovery Enhancement delivered via tele-health.
Treatment:
Behavioral: Mindfulness-Oriented Recovery Enhancement

Trial documents
2

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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