App therapy tackles mental health in opioid treatment
NCT ID NCT05047627
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tested a smartphone app designed to reduce anxiety and depression in people already receiving medication for opioid use disorder. 63 adults were randomly assigned to use the app for four weeks or to continue their usual care. The goal was to see if the app was feasible and acceptable, and to get early data on whether it could improve mental health and reduce opioid cravings and use.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Smartphone-based digital intervention (cognitive-behavioral therapy app)
- What this could lead to
- If it works, this could provide a low-cost, scalable way to treat anxiety and depression in people receiving medication for opioid use disorder, potentially improving overall outcomes.
- What could go wrong
- This was a small, early feasibility study with only 63 participants and no control for the app's specific effects. The intervention was still being developed, so results may not be generalizable.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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63 people
The number who actually took part.
- Started
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Sep 2021
- Finished
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Mar 2023
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Adults (age 18 or older) * fluent in English * able to provide informed consent * meet current criteria for OUD (as defined by a Rapid Opioid Dependence Screen) * are receiving methadone, buprenorphine, and/or naltrexone for OUD * meet current criteria for an anxiety and/or depressive disorder (based on the Patient Health Questionnaire and the Generalized Anxiety Disorder Questionnaire). Exclusion Criteria: * active suicidality * psychosis * bipolar disorder
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Center For Technology and Behavioral Health
Lebanon, New Hampshire, 03766, United States
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