Substance Use Disorders Clinical Trial
— CRAFT-EPIOfficial title:
Adapting Community Reinforcement Approach and Family Training to Target Substance Use in Early Psychosis Intervention: A Pilot Study of Group Therapy
Verified date | September 2023 |
Source | Centre for Addiction and Mental Health |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The goal of this pilot feasibility and proof of concept study is to evaluate whether Community Reinforcement and Family Training (CRAFT) as adapted for group delivery in an early psychosis intervention (EPI) program has a clinically significant impact on the concerned significant other (CSO) and Identified patient (IP), and whether a larger, definitive trial is feasible. The intervention aims to improve treatment engagement and reduce distress, as reported by the CSO. To assess feasibility of the intervention for a definitive trial of CRAFT-EPI, the investigators will evaluate recruitment, retention, and assessment completion rates.
Status | Completed |
Enrollment | 14 |
Est. completion date | September 28, 2022 |
Est. primary completion date | September 28, 2022 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: Concerned significant other (CSO) - Adult (at least 18 years) family member of an identified patient (IP) enrolled in SCEI treatment. The IP should be aged 16-29 years with clinician diagnosis of early psychosis (schizophrenia, schizoaffective disorder, schizophreniform disorder, bipolar I disorder, major depressive disorder with psychotic features, substance-induced psychotic disorder, or unspecified schizophrenia spectrum and other psychotic disorder). The IP does NOT need to be enrolled in the study in order for the CSO to participate. Up to 2 CSOs associated with the same IP may participate. - Has completed the program's introductory psychoeducation group - Concerned about substance use in the IP enrolled in the early psychosis intervention program Identified patient - Enrolled in the early psychosis intervention program, aged 16-29 years with clinician diagnosis of early psychosis (schizophrenia, schizoaffective disorder, schizophreniform disorder, bipolar I disorder, major depressive disorder with psychotic features, substance-induced psychotic disorder, or unspecified schizophrenia spectrum and other psychotic disorder) - Not currently receiving specialized substance use treatment (i.e. by a clinician other than their NAVIGATE clinicians) Exclusion Criteria: Concerned significant other - Inability to provide informed consent - Inability to communicate in basic oral and written English. - There are already 2 CSOs associated with a given IP that are participating in the CRAFT-EPI study. - Lack of a device for videoconferencing and a secure Wi-Fi connection - Unwilling to turn camera on for weekly group sessions (except in the case of a poor Wi-Fi connection, or other similar circumstances) Identified patient - Does not have a CSO that is enrolled in the CRAFT-EPI study - Inability to provide informed consent - Inability to communicate in basic oral and written English |
Country | Name | City | State |
---|---|---|---|
Canada | Centre for Addiction and Mental Health | Toronto | Ontario |
Lead Sponsor | Collaborator |
---|---|
Centre for Addiction and Mental Health | Mclean Hospital |
Canada,
Meyers RJ, Miller WR, Hill DE, Tonigan JS. Community reinforcement and family training (CRAFT): engaging unmotivated drug users in treatment. J Subst Abuse. 1998;10(3):291-308. doi: 10.1016/s0899-3289(99)00003-6. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Rate of treatment entry for substance use | Treatment entry for substance use by the identified patient as reported by their family member (concerned significant other) | 18 weeks | |
Primary | Rates of recruitment | Number of family member and identified patient participants who consent to participation | Baseline | |
Primary | Rates of retention | Number of family member participants who complete 6 intervention sessions and booster session | 18 weeks | |
Primary | Rates of assessment completion | Proportion of assessments completed by consented family members and identified patients, averaged over 3 timepoints | 18 weeks | |
Secondary | Patient Health Questionnaire (PHQ-9) total score | Symptoms of depression | Baseline, 6 weeks, 18 weeks | |
Secondary | Happiness Scale total score | Experience of happiness | Baseline, 6 weeks, 18 weeks | |
Secondary | Perceived Stress Scale-14 item total score | Experience of stress | Baseline, 6 weeks, 18 weeks | |
Secondary | Ontario Perception of Care Tool-Mental Health and Addictions section scores | Perceptions of care, satisfaction with the model | 6 weeks, 18 weeks | |
Secondary | Contemplation Ladder total score | Readiness to change substance use | Baseline, 6 weeks, 18 weeks | |
Secondary | National Institute on Drug Abuse (NIDA)-Modified Alcohol, Smoking and Substance Involvement Screening Test (ASSIST) V2.0 total score | Substance use | Baseline, 6 weeks, 18 weeks | |
Secondary | Generalized Anxiety Disorder-7 (GAD-7) total score | Symptoms of anxiety | Baseline, 6 weeks, 18 weeks |
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