Feasibility of Providing Computerized CBT in the Black Church

NCT ID: NCT03579290

Last Updated: 2024-03-08

Study Results

Results available

Outcome measurements, participant flow, baseline characteristics, and adverse events have been published for this study.

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Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

40 participants

Study Classification

INTERVENTIONAL

Study Start Date

2018-05-24

Study Completion Date

2018-10-30

Brief Summary

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The investigator will conduct a pilot study evaluating the feasibility and acceptability of providing a computer-based program (CBT4CBT), used for the treatment of substance use disorders, in a church setting.

Detailed Description

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The investigator will conduct a pilot study evaluating the feasibility and acceptability of providing a computer-based program (CBT4CBT), used for the treatment of substance use disorders, in a church setting. Forty Black adults with a current DSM-5 alcohol or substance use disorder will utilize the 'CBT for CBT' program over a period of 8 weeks. Primary outcomes will be acceptability and feasibility of providing the treatment in a church setting. If found to be acceptable and feasible, with preliminary promise for reductions in substance use, the next step would be to adapt the computer intervention for this population and conduct a randomized controlled trial.

Conditions

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Substance Abuse

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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CBT4CBT program

The 'CBT for CBT' program is modeled closely on our NIDA-published CBT manual. Seven core skill modules will cover the following topics, which correspond to the major session topics in the manual:

Understanding and changing patterns of drug use, Coping with craving, Substance refusal skills, Seemingly irrelevant decisions, Planning for emergencies, and Problem-solving skills. Staying Safe

Group Type EXPERIMENTAL

CBT4CBT program

Intervention Type BEHAVIORAL

The 'CBT for CBT' program is modeled closely on our NIDA-published CBT manual. Seven core skill modules will cover the following topics, which correspond to the major session topics in the manual:

* Understanding and changing patterns of drug use,
* Coping with craving,
* Substance refusal skills,
* Seemingly irrelevant decisions,
* Planning for emergencies, and
* Problem-solving skills.
* Staying Safe

Interventions

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CBT4CBT program

The 'CBT for CBT' program is modeled closely on our NIDA-published CBT manual. Seven core skill modules will cover the following topics, which correspond to the major session topics in the manual:

* Understanding and changing patterns of drug use,
* Coping with craving,
* Substance refusal skills,
* Seemingly irrelevant decisions,
* Planning for emergencies, and
* Problem-solving skills.
* Staying Safe

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* At least 18 years of age
* Has at least one SUD diagnosis as defined by the DSM 5

Exclusion Criteria

* Are unable provide informed consent or participate in the study procedures as proposed in the consent
* Active suicidal or homicidal ideation
* Current engagement in substance use treatment
* Have a current legal case pending, such that incarceration during the 8 week protocol is likely
* Are in need of detoxification from alcohol, opioids or benzodiazepines
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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National Institutes of Health (NIH)

NIH

Sponsor Role collaborator

National Institute on Drug Abuse (NIDA)

NIH

Sponsor Role collaborator

Yale University

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Ayana Jordan, MD; PhD

Role: PRINCIPAL_INVESTIGATOR

Yale University

Locations

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Dixwell Ave Congregational United Church of Christ

New Haven, Connecticut, United States

Site Status

Countries

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United States

Provided Documents

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Document Type: Study Protocol

View Document

Document Type: Statistical Analysis Plan

View Document

Document Type: Informed Consent Form

View Document

Other Identifiers

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KL2TR001862

Identifier Type: NIH

Identifier Source: secondary_id

View Link

5R25DA035163-03

Identifier Type: NIH

Identifier Source: secondary_id

View Link

2000022733

Identifier Type: -

Identifier Source: org_study_id

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