Alcohol Use Disorder Clinical Trial
Official title:
Integrating Contingency Management Into Routine Care for Alcohol Use Disorder
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 |
Verified date | August 2020 |
Source | DynamiCare Health |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
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)
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. |
Country | Name | City | State |
---|---|---|---|
United States | Gosnold on Cape Cod | Centerville | Massachusetts |
United States | Gosnold | Falmouth | Massachusetts |
Lead Sponsor | Collaborator |
---|---|
DynamiCare Health | Johns Hopkins University |
United States,
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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