Co-Active Therapeutic Theatre (Co-ATT) for Dual-Diagnosis Patients

NCT ID: NCT06187701

Last Updated: 2025-04-01

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

NOT_YET_RECRUITING

Clinical Phase

NA

Total Enrollment

10 participants

Study Classification

INTERVENTIONAL

Study Start Date

2026-03-31

Study Completion Date

2027-12-31

Brief Summary

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Drama Therapy involves of the use of theatrical techniques (such as script development, acting exercises, improvisation, etc.) to help treat patients' mental illness and improve their functioning and overall sense of wellbeing.

This study will evaluate the effectiveness of a specific version of drama therapy for the treatment of patients suffering from both mental illness (such as depression, bipolar disorder, schizophrenia, etc.) and one or more substance use disorders. The study will also assess participants feelings and thoughts about the drama therapy intervention (such as whether or not they enjoyed it and if/how they found it helpful).

The drama therapy intervention will consist of one group drama therapy session per week, for a total of twelve weeks (i.e., total twelve sessions) followed by a single performance (with composition of the audience determined by unanimous agreement of the participants) of the dramatic work (script) produced by the participants during the course of the drama therapy intervention.

Detailed Description

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Conditions

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Mental Health Issue Substance Use Disorders

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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Co-Active Therapeutic Theatre (Co-ATT)

Drama therapy will be used to treat participants with co-occurring primary psychiatric and substance use disorders

Group Type EXPERIMENTAL

Co-Active Therapeutic Theatre (Co-ATT)

Intervention Type BEHAVIORAL

There will be one group drama therapy session per week, for a total of twelve weeks (i.e., total twelve sessions) followed by a single performance (with composition of the audience determined by unanimous agreement of the participants) of the dramatic work (script) produced by the participants during the course of the drama therapy intervention.

Interventions

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Co-Active Therapeutic Theatre (Co-ATT)

There will be one group drama therapy session per week, for a total of twelve weeks (i.e., total twelve sessions) followed by a single performance (with composition of the audience determined by unanimous agreement of the participants) of the dramatic work (script) produced by the participants during the course of the drama therapy intervention.

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* Diagnosed with at least one primary psychiatric disorder, and
* Diagnosed with at least one substance use disorder
* Both disorders active (i.e., meeting DSM-V criteria for each disorder (i.e., with ongoing psychiatric symptoms and ongoing substance use)
* Enrolled in the Addiction Psychiatry Treatment Program (APTP) at Boston Medical Center (i.e., scheduled for follow-up appointments with therapist and/or psychiatrist in APTP).
* Currently taking medications and those not currently taking medications

Exclusion Criteria

* Incarcerated persons
* Pregnant women
* Inability to understand and/or sign informed consent form
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Boston Medical Center

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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William-Bernard Reid-Varley, MD MPH

Role: PRINCIPAL_INVESTIGATOR

Boston Medical Center, Psychiatry Department

Locations

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Boston Medical Center

Boston, Massachusetts, United States

Site Status

Countries

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United States

Central Contacts

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William-Bernard Reid-Varley, MD MPH

Role: CONTACT

617-638-8014

Facility Contacts

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William-Bernard Reid-Varley, MD MPH

Role: primary

617-638-8014

Other Identifiers

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H-43656

Identifier Type: -

Identifier Source: org_study_id

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