Counseling to improve adherence to the taking of medications for tuberculosis in Bali, Indonesia
- Conditions
- Medication adherence and treatment success in patients with tuberculosisInfections and Infestations
- Registration Number
- ISRCTN18141422
- Lead Sponsor
- dayana University
- Brief Summary
2021 Results article in https://pubmed.ncbi.nlm.nih.gov/34948846/ (added 16/02/2022)
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 214
For the interventional trial:
1. New patients who are diagnosed with early pulmonary TB based on records registered with TB in the health center and have never received OAT
2. Patients diagnosed with pulmonary tuberculosis, the treatment has not yet passed the two-month treatment period (intensive phase), seen from the records in the public health center TB register
3. Based on the register, the patient was diagnosed with pulmonary TB through a bacteriological examination (positive smear) using the Molecular Rapid Test (TCM)
4. Adult patients aged 18 - 65 years
For qualitative data collection:
1. Patients who have received HBM-based MI intervention
1.1. Non-compliance with taking medication
1.2. Failure in treatment
1.3. Able to communicate well and willing to be informants.
1.4. Own and be able to use a smartphone
1.5. Willing to be interviewed using online media via telephone/video call for approximately 30 minutes
2. Officer/counsellor
2.1. Easy contact to communicate
2.2. Own and be able to use a smartphone
2.3. Able to communicate well and willing to be informants
2.4. Willing to be interviewed using online media via telephone/video call for approximately 30 minutes
For interventional trial:
1. MDR TB patients who are registered in the TB register
2. Have other comorbidities such as diabetes mellitus, cirrhosis of the liver, hepatitis; cardiovascular disease based on the doctor's examination on the TB register
3. Patients are not willing to follow Tuberculosis treatment until the advanced phase
4. Families of sufferers do not have/are unable to use a smartphone
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method