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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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12 December 2020 |
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Main ID: |
NCT01297985 |
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Date of registration:
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16/02/2011 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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A Randomized Controlled Trial of Mental Health Peer-Led Education
BRIDGES |
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Scientific title:
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Efficacy of Peer-Led Education in Improving Mental Health Recovery Outcomes in Tennessee |
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Date of first enrolment:
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January 2006 |
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Target sample size:
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428 |
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Recruitment status: |
Completed |
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URL:
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https://clinicaltrials.gov/show/NCT01297985 |
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Study type:
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Interventional |
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Study design:
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Allocation: Randomized. Intervention model: Parallel Assignment. Primary purpose: Health Services Research. Masking: Single (Outcomes Assessor).
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Phase:
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N/A
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Countries of recruitment
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United States
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Contacts
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Name:
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Judith A Cook, PhD |
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Address:
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Telephone:
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Email:
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Affiliation:
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Department of Psychiatry, University of Illinois at Chicago |
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Name:
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Susan A Pickett, PhD |
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Address:
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Telephone:
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Email:
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Affiliation:
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Department of Psychiatry, University of Illinois at Chicago |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- Clinical diagnosis of mental illness
- Disability due to mental illness
- Age 18 years or older
- Willingness to receive the intervention
Exclusion Criteria:
- Inability to understand spoken English
Age minimum:
18 Years
Age maximum:
N/A
Gender:
All
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Health Condition(s) or Problem(s) studied
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Mental Disorders
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Intervention(s)
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Behavioral: BRIDGES Peer-Led Education
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Primary Outcome(s)
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Recovery From Mental Illness
[Time Frame: Study entry (Pre-intervention/T1), 8-weeks later (Post-Intervention 1/T2), & 6-months after T2 (Post-Intervention 2/T3)]
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Personal Empowerment
[Time Frame: Study entry (Pre-intervention/T1), 8-weeks later (Post-Intervention 1/T2), & 6-months after T2 (Post-Intervention 2/T3)]
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Secondary Outcome(s)
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Patient Self-advocacy
[Time Frame: Study entry (Pre-intervention/T1), 8-weeks later (Post-Intervention 1/T2), & 6-months after T2 (Post-Intervention 2/T3)]
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Hopefulness
[Time Frame: Study entry (Pre-intervention/T1), 8-weeks later (Post-Intervention 1/T2), & 6-months after T2 (Post-Intervention 2/T3)]
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Coping Style
[Time Frame: Study entry (Pre-intervention/T1), 8-weeks later (Post-Intervention 1/T2), & 6-months after T2 (Post-Intervention 2/T3)]
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Secondary ID(s)
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H133B050003b
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2006-0024
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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