Measuring HIV-related mortality during surveys in Africa
Not Applicable
Completed
- Conditions
- HIV status of deceased siblingInfections and InfestationsHuman immunodeficiency virus [HIV] disease
- Registration Number
- ISRCTN15197669
- Lead Sponsor
- ational Institute of Allergy and Infectious Diseases (NIAID)
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 535
Inclusion Criteria
1. Aged 15-59 years old at the time of the study
2. Residing in the Karonga Health and Demographic Surveillance System (HDSS) area
Exclusion Criteria
1. Younger than 15 years old at the time of enrollment
2. Older than 59 years old at the time of enrollment
6. Not residing in the Karonga Health and Demographic Surveillance System (HDSS) area
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <br> 1. Sensitivity in recording the HIV status of deceased siblings in the ACASI and face-to-face groups. Sensitivity is defined as the proportion of HIV positive deaths according to KHDSS that were correctly reported as such by survey respondents.<br> 2. Specificity in recording the HIV status of deceased siblings in the ACASI and face-to-face groups. Specificity is defined as the proportion of HIV-negative deaths according to KHDSS that were correctly reported as such by survey respondents.<br> There will be one planned study visit per participant, with no planned follow-up. As such the outcomes will be measured at the one study visit. The trialists will measure the level of agreement between survey data and KHDSS data using Cohen’s Kappa in each study arm.<br>
- Secondary Outcome Measures
Name Time Method <br> 1. The sensitivity/specificity of the survey in recording the respondent's own HIV status<br> 2. The amount of time spent answering HIV-related questions, as measured internally by ODK<br> 3. The accuracy of the enhanced questionnaire in assessing the engagement of deceased siblings identified as HIV-infected on the HIV care cascade<br> There will be one planned study visit per participant, with no planned follow-up. As such the outcomes will be measured at the one study visit.<br>