NCT05047627

Brief Summary

The majority of opioid users meet criteria for anxiety and depressive disorders, but most substance use disorder treatment programs do not offer treatment for co-occurring mental health problems. Anxiety and depression may also be directly linked to opioid use itself. Although treatments have been developed for anxiety and depressive symptoms for opioid users within face-to-face settings, few treatment facilities offer these in-person interventions due to their high cost and time burden. Given the deficits in research on treatments for anxiety and depression among those with opioid use disorder, the current research will examine the efficacy of a digital intervention designed to treat anxiety and depressive symptoms by augmenting the state of the science medication-based opioid use disorder treatment. Over the course of the proposed study, the research team will design and test the feasibility and acceptability of a standalone mobile intervention designed to treat persons receiving medication treatment for opioid use disorder. Participants receiving medication treatment for opioid use disorder will be randomized to receive a digital intervention to treat anxiety and depression or care as usual for a total of four weeks. The overarching goal of the proposed work is to test the feasibility and acceptability of the proposed mobile intervention. The Investigators will also explore the preliminary efficacy by examining reductions in anxiety and depressive symptoms and opioid cravings and use. This work could lead to a low-cost scalable solution to augment gold-standard treatment as usual in opioid use disorder by decreasing levels of comorbidity of anxiety and depressive disorders, thereby ultimately improving the outcomes of opioid use disorder itself.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
63

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Sep 2021

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

August 13, 2021

Completed
1 month until next milestone

Study Start

First participant enrolled

September 15, 2021

Completed
2 days until next milestone

First Posted

Study publicly available on registry

September 17, 2021

Completed
1.3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2022

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

March 1, 2023

Completed
2.7 years until next milestone

Results Posted

Study results publicly available

November 5, 2025

Completed
Last Updated

November 5, 2025

Status Verified

October 1, 2025

Enrollment Period

1.3 years

First QC Date

August 13, 2021

Results QC Date

November 21, 2024

Last Update Submit

October 16, 2025

Conditions

Outcome Measures

Primary Outcomes (3)

  • Change in Anxiety Symptoms as Assessed by Generalized Anxiety Disorder- Q-IV Scale

    Assesses anxiety symptoms. Possible GAD-Q-IV scores range from 0 to 12, with higher scores representing greater GAD symptom severity

    From Baseline to 4 weeks (post-intervention) and from Baseline to 8 weeks (follow-up).

  • Change in Depressive Symptoms as Assessed by Patient Health Questionnaire-9

    Assesses depressive symptoms, the PHQ-9 score can range from 0 to 27, since each of the 9 items can be scored from 0 (not at all) to 3 (nearly every day)

    From Baseline to 4 weeks (post-intervention) and from Baseline to 8 weeks (follow-up).

  • Change in Likelihood of a Positive Urine Screen for Opioids (MOP)

    This outcome measures the change in the likelihood of a positive urine drug screen (UDS) for opioids (MOP). The result of each UDS was coded as a binary variable (0 = negative test, 1 = positive test). The reported data are the beta coefficients (estimated mean change) from a robust linear mixed-effects model, which are presented on a unitless scale. A negative value indicates a reduction in the likelihood of testing positive and represents a better outcome.

    From Baseline to 4 weeks (post-intervention) and from Baseline to 8 weeks (follow-up).

Secondary Outcomes (2)

  • Change in Opioid Use Disorder Severity as Measured by the Rapid Opioid Dependence Screen (RODS)

    From Baseline to 4 weeks (post-intervention) and from Baseline to 8 weeks (follow-up).

  • Change in Opioid Craving as Measured by the Opioid Craving Scale (OCS)

    From Baseline to 4 weeks (post-intervention) and from Baseline to 8 weeks (follow-up).

Study Arms (2)

Smartphone Digital Intervention Group

EXPERIMENTAL

The Smartphone Digital Intervention Group is the experimental group. Participants randomized to this group will download the smartphone intervention and be asked to use the intervention four times per week for four weeks ( 16 digital sessions). The smartphone digital intervention will also continuously collect passive sensing data. The smartphone digital intervention will be designed to treat anxiety and depression by providing informational videos to help participants treat these symptoms. These videos include information about physical activity, muscle relaxation, and other proven helpful interventions to help with anxiety and depression.

Behavioral: Smartphone-Based Digital Intervention

Wait list Control Condition

NO INTERVENTION

The wait list control condition will not receive the digital intervention treatment for the duration of the study. They will still provide urine samples during the study. Participants assigned to this condition will be able to access the digital intervention after their participation in the study.

Interventions

The digital intervention will be a prototype, and the current trial will be used to continue to both develop and refine the intervention. The current intervention will be based on a combination of cognitive-behavioral principles. As with prior research, the mobile platform will be delivered via Qualtrics, a HIPAA compliant and mobile-friendly platform. The cognitive-behavioral therapy will be primarily based on components with strongest support in digital interventions. The app will continuously collect passive sensing data on patterns in 1) sleep duration and quality;(2) light (3) location; (4) movement (5) social contact including duration and frequency of incoming and outcoming calls and text messages; (6) screen time; and (7) heart rate variability; (8) sound levels captured through passively collected smartphone The platform will deliver interactive interventions where participants will view texts and images, and it will also allow user interaction.

Smartphone Digital Intervention Group

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • 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).

You may not qualify if:

  • active suicidality
  • psychosis
  • bipolar disorder

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Center For Technology and Behavioral Health

Lebanon, New Hampshire, 03766, United States

Location

Related Publications (34)

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    BACKGROUND

MeSH Terms

Conditions

Opioid-Related DisordersAnxiety DisordersDepressive Disorder

Condition Hierarchy (Ancestors)

Narcotic-Related DisordersSubstance-Related DisordersChemically-Induced DisordersMental DisordersMood Disorders

Results Point of Contact

Title
Nicholas Jacobson
Organization
Dartmouth College

Study Officials

  • Nicholas C Jacobson, PhD

    Dartmouth College

    PRINCIPAL INVESTIGATOR

Publication Agreements

PI is Sponsor Employee
Yes

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

August 13, 2021

First Posted

September 17, 2021

Study Start

September 15, 2021

Primary Completion

December 31, 2022

Study Completion

March 1, 2023

Last Updated

November 5, 2025

Results First Posted

November 5, 2025

Record last verified: 2025-10

Data Sharing

IPD Sharing
Will not share

Locations