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A Chatbot to Support Substance Use Recovery

D

Dimagi

Status and phase

Enrolling
Phase 2
Phase 1

Conditions

Opiate Substitution Treatment
Opiate-Related Disorders

Treatments

Other: chatbot

Study type

Interventional

Funder types

Other
Industry
NIH

Identifiers

NCT06845878
2R44DA050218-02 (U.S. NIH Grant/Contract)
2R44DA050218 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

The goal of this clinical trial is to learn if/how an AI chatbot can support patients who in recovery for substance use, specifically those who are receiving medication for opioid use disorder.

Can the chatbot help lower drug use? Can the chatbot help improve clinical appointment adherence? Can the chatbot help patients build self-efficacy in leading their own recovery journey? Will the chatbot help reduce workload burden for primary care teams? Can the chatbot serve as a safe, useful and engaging tool to support patients?

Researchers will investigate the effects of using a chatbot to support follow-up care for patients in opioid use recovery.

Participants will:

  • Receive access to a chatbot for 12 weeks that they can use to prepare for upcoming clinical appointments, find community resources, learn about urge-surfing and wellness techniques, and query for assistance with other recovery-related information and tasks
  • Complete surveys and provide user feedback

Enrollment

55 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 18-65 years old
  • Comfortable with reading, understanding, and communicating in English
  • Receiving medication treatment for OUD at MGH?
  • Able to participate in a remote interview?
  • Own or have reliable access to Wi-Fi or a cellular network
  • Willing to use a mobile device to access the chatbot?

Exclusion criteria

  • Has any cognitive, visual, or auditory impairments that may prevent the participant from using the chatbot on a mobile device?
  • Unstable medical condition that compromises the ability to safely participate

Trial design

Primary purpose

Health Services Research

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

55 participants in 1 patient group

Chatbot
Experimental group
Description:
Participants will receive access to a chatbot for 12 weeks that can be used from a mobile device to support follow-up care and recovery needs.
Treatment:
Other: chatbot

Trial contacts and locations

1

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Central trial contact

Dimagi Study Team

Data sourced from clinicaltrials.gov

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