RECRUITING

Women's Opioid Treatment Follow-up Study

Description

The goal of this study is to examine the feasibility of a gender-specific digital intervention for women with opioid use disorder. In this study, women with opioid use disorder will be randomized to receive treatment-as-usual plus a gender-specific digital intervention or treatment-as-usual only. Feasibility, satisfaction, and engagement with the intervention are the primary outcomes and will be measured post-intervention and at two-week, 6-week, and 12-week follow-up visits.

Study Overview

Study Details

Study overview

The goal of this study is to examine the feasibility of a gender-specific digital intervention for women with opioid use disorder. In this study, women with opioid use disorder will be randomized to receive treatment-as-usual plus a gender-specific digital intervention or treatment-as-usual only. Feasibility, satisfaction, and engagement with the intervention are the primary outcomes and will be measured post-intervention and at two-week, 6-week, and 12-week follow-up visits.

Increasing Women's Engagement in Medication Treatment for Opioid Use Disorder Through Digital Intervention

Women's Opioid Treatment Follow-up Study

Condition
Opioid Use Disorder
Intervention / Treatment

-

Contacts and Locations

Belmont

McLean Hospital, Belmont, Massachusetts, United States, 02478-1064

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * age 18 years of age or older
  • * current opioid use disorder diagnosis
  • * have a smartphone
  • * initiated medication treatment for opioid use disorder in the past 30 days,
  • * able to provide informed consent
  • * an acute psychiatric or medical condition, or cognitive impairment, that would impair the ability to complete study procedures
  • * admitted to their current treatment episode on an involuntary status

Ages Eligible for Study

18 Years to

Sexes Eligible for Study

FEMALE

Accepts Healthy Volunteers

No

Collaborators and Investigators

Mclean Hospital,

Study Record Dates

2025-06