The effectiveness of a self-stigma reduction intervention upon stigma measures for patients with tuberculosis (TB) and multidrug-resistant tuberculosis (MDR-TB) in Vietnam: a randomised controlled trial
- Conditions
- Mental Health - DepressionstigmadepressiontuberculosisPublic Health - Health promotion/educationInfection - Other infectious diseasesmultidrug-resistant tuberculosis
- Registration Number
- ACTRN12619000949189
- Lead Sponsor
- niversity of Sydney
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot yet recruiting
- Sex
- All
- Target Recruitment
- 268
Patients with bacteriologically proven pulmonary TB and Patients with bacteriologically proven pulmonary RR/MDR-TB, be undertaking treatment for within the NTP at the participating health facilities and be considered as non-infectious will be eligible to participate. To be considered as non-infectious, they require 1) reduction in symptoms AND, 2) reduction in smear grade, culture negative for last 4 weeks OR unable to produce sputum AND 3) completed at least 2 weeks of treatment for patients with TB or 6 weeks of treatment for patients with RR/MDR-TB.
Unable to participate in the intervention
People that are incarcerated
Do not live in the study location, Hanoi, Vietnam
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Evaluate the effect of a self-stigma and shame workshop (the intervention) upon the self-stigma of patients with RR/MDR-TB, measured according to a validated self-stigma scale (the Redwood self-stigma subscale).[4 months after baseline. The intervention will be delivered between baseline and 2 months.];Evaluate the effect of the intervention upon the measured stigma of patients with new TB, measured according to a validated self-stigma scale (the Redwood self-stigma subscale).[4 months after baseline. The intervention will be delivered between baseline and 2 months.]
- Secondary Outcome Measures
Name Time Method