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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03701204
Other study ID # DCH001
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date October 8, 2018
Est. completion date August 21, 2019

Study information

Verified date August 2020
Source DynamiCare Health
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Randomized pilot study of a device (smartphone app) that poses non-significant risk to participants and is exempt from Investigational Device Exemption regulations [21 Code of Federal Regulations 812.2(c)


Description:

To test the feasibility/acceptability and efficacy of a minimum viable product (MVP) of a smartphone app for patients with alcohol use disorder who are in active treatment and recovery to perform self-tracking of their recovery behavior (e.g., abstinence) and focus on their motivation to maintain their desired health behaviors (i.e., abstinence).


Recruitment information / eligibility

Status Completed
Enrollment 61
Est. completion date August 21, 2019
Est. primary completion date August 21, 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

Participants in the pilot study will be 60 new intakes to Gosnold's outpatient Substance Use Disorder (SUD) program who:

- are >18 years old;

- meet DSM-5 criteria for current (past year) alcohol use disorder, at least moderate severity;

- identify alcohol as the primary drug problem;

- Currently use alcohol (past 7 days) or have been in treatment 14 days or less and used alcohol within 7 days of treatment entry;

- have and use an Android or iOS smartphone with acceptable

- capability;

- are willing to participate in home testing and use of the smartphone,

- speak and read the English language adequately to understand smartphone commands and responses and

- are willing to be randomly assigned to receive treatment with or without the smartphone app as an added feature.

Exclusion Criteria:

• Participants must not currently be suicidal or actively psychotic, by clinician judgement.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
DynamiCare Rewards
Participants assigned to the DynamiCare Rewards group will receive the following: App on their smartphone Substance Testing Devices: BACTrack Mobile Pro - submits BAC results directly to smartphone via Bluetooth and Saliva Test Kits. Next Step debit card to receive financial incentives Participant will be prompted via the app to conduct breathalyzer/saliva tests, using the devices camera to take "selfie" photo/videos to prevent cheating. Negative tests result in participant receiving electronic virtual "coins", which can be transferred from reserve account (reserve account inaccessible to participant) to the spendable Next Step debit card. The amount of coins and funds are available on a progressive variable reward schedule.

Locations

Country Name City State
United States Gosnold on Cape Cod Centerville Massachusetts
United States Gosnold Falmouth Massachusetts

Sponsors (2)

Lead Sponsor Collaborator
DynamiCare Health Johns Hopkins University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Percent of participants abstinent from alcohol at each monthly assessment time point (negative urine test and self-report of no use in past 30 days) The pilot efficacy study will utilize alcohol abstinence at each assessment time point as the primary outcome. This is defined as a negative ethyl glucuronide urine test (witnessed) at the monthly assessment time points and self-report of no alcohol use in the past 30 days. 12-week intervention period
Secondary Percent of participants abstinent from all drugs at each monthly assessment time point (negative urine test and self-report of no use in past 30 days) Groups will be compared using Generalized Estimating Equation (GEE) analysis on the percent of participants abstinent over time at each time point. 12-week intervention period
Secondary Longest continuous period of abstinence from alcohol and from drugs and alcohol Groups will be compared using GEE analysis on the percent of participants abstinent over time at each time point. 12-week intervention period
Secondary Retention in treatment Groups will be compared on the number of days retained in treatment according to the site's Electronic Health Record data, and also on the graduation rate from treatment vs. leaving against medical advice. 12-week intervention period
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