Maternal Depression Clinical Trial
— THP-TACTSOfficial title:
Effectiveness of Technology Assisted Cascade Training and Supervision of Community Health Workers in Delivering Thinking Healthy Program for Perinatal Depression in a Post-conflict Area of Pakistan- Protocol of a Randomized Controlled Trial
Verified date | February 2017 |
Source | Human Development Research Foundation, Pakistan |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The Thinking Healthy Program is evidence based psychological intervention, delivered by non-specialists, with proven impact on maternal depression. A major challenge in the scale-up of this intervention, especially where health systems are weak, is providing quality training and supervision at scale. Women living in post-conflict areas are at a higher risk of depression than the general population.The key innovation proposed is the development and evaluation of a technology-assisted cascade training and supervision system to assist scale-up of the Thinking Healthy Programme in a post conflict area of Pakistan.
Status | Completed |
Enrollment | 80 |
Est. completion date | October 2016 |
Est. primary completion date | September 2016 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | N/A and older |
Eligibility |
Inclusion Criteria: - Lady health workers currently working in Swat district Exclusion Criteria: - Physically unwell, lady health workers on leave |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Human Development Research Foundation, Pakistan | Duke University, University of Liverpool |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Competency of health workers in THP skills measured using ENact assessment tool | The competency of health workers in the two arms will be measured using ENact assessment tool. | Immediately after intervention | |
Secondary | Cost of intervention | Cost of intervention and comparative arm will be assessed from data collected during the trial and analyzed after 3 months. | 3 months after intervention |
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