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NCT01887665 Clinical Trial

Enhancing Early-Phase Care for Primary Care Patients With Unhealthy Substance Use

Substance Use Disorders Clinical Trial

Official title:
Enhancing Early-Phase Care for Primary Care Patients With Unhealthy Substance Use

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01887665
Other study ID # 12116
Secondary ID 1R21DA032039-01A
Status Completed
Phase N/A
First received June 25, 2013
Last updated March 2, 2016
Start date August 2013
Est. completion date March 2016

Study information
Verified date March 2016
Source Brandeis University
Contact n/a
Is FDA regulated No
Health authority United States: Data and Safety Monitoring BoardUnited States: Federal GovernmentUnited States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

The clinical trial portion of this study tests the hypothesis that contingency management-based incentives for primary care patients with substance use disorders to attend treatment services will increase treatment initiation and engagement. The investigators are investigating whether this approach that has been found effective in specialty treatment settings will work in the primary care context, in conjunction with screening.

Recruitment information / eligibility
Status Completed
Enrollment 13
Est. completion date March 2016
Est. primary completion date December 2015
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Positive self-report alcohol or drug use screen in primary care

- Diagnosis of substance use disorder

- age 18 or older

Exclusion Criteria:

- SUD treatment in past 60 days

- cognitive impairment

Study Design

Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Intervention

Behavioral:
• incentives
A structured system of prize-based financial incentives rewards attendance at treatment visits.

Locations
Country Name City State
United States Edith Nourse VA Medical Center (Bedford VA) Bedford Massachusetts

Sponsors (2)
Lead Sponsor Collaborator
Brandeis University National Institute on Drug Abuse (NIDA)

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Initiation Had initial outpatient treatment visit following positive screen and confirmatory diagnosis 90 days No
Primary Engagement Had two additional outpatient treatment visits after initiating treatment 90 days No
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