Mental Health in Adults and Children- Frugal Innovations (MAC-FI): Adult Depression Component (MAC-FI)
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|ClinicalTrials.gov Identifier: NCT03001063|
Recruitment Status : Recruiting
First Posted : December 22, 2016
Last Update Posted : December 23, 2016
|Condition or disease||Intervention/treatment||Phase|
|Depression||Other: Supported Self-Management Other: Enhanced treatment as usual||Not Applicable|
|Study Type :||Interventional (Clinical Trial)|
|Estimated Enrollment :||256 participants|
|Intervention Model:||Parallel Assignment|
|Masking:||Single (Outcomes Assessor)|
|Official Title:||Mental Health in Adults and Children: Frugal Innovations|
|Study Start Date :||March 2016|
|Estimated Primary Completion Date :||January 2019|
|Estimated Study Completion Date :||March 2019|
This arm will receive the Supported Self- Management intervention, which consists of bibliotherapy that is provided with the regular support of health or social workers for a duration of two months.
Other: Supported Self-Management
This Supported Self-Management intervention consists of bibliotherapy (the Antidepressant Skills Workshop) that is provided to a patient by a health or social worker. The patient is supported in the use of the skills found in the workbook over the course of two months. The skills in the workbook are based on the principles of Cognitive Behavioural Therapy.
This arm will receive enhanced treatment as usual, which consists of a leaflet with information about depression and regular care as provided by primary care centres. The control arm will receive the intervention after the intervention arm has completed the intervention period.
Other: Enhanced treatment as usual
Participants in the control arm will received enhanced treatment as usual in the form of usual care at primary care centres and a leaflet providing information about depression.
- Self-Reporting Questionnaire 20 (SRQ-20) [ Time Frame: Two months ]
- World Health Organization's Disability Assessment Scale (WHODAS 2.0) [ Time Frame: Two months ]
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03001063
|Contact: Jill Murphy, PhDfirstname.lastname@example.org|
|Contact: Rebecca Zappelli, BAemail@example.com|
|Institute of Population, Health and Development||Recruiting|
|Contact: Vu Cong Nguyen, MD firstname.lastname@example.org|
|Principal Investigator:||John O'Neil, PhD||Simon Fraser University|
|Principal Investigator:||Vu Cong Nguyen, MD||Institute of Population, Health and Development|