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Measuring HIV-related mortality during surveys in Africa

Not Applicable
Completed
Conditions
HIV status of deceased sibling
Infections and Infestations
Human 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
NameTimeMethod
<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
NameTimeMethod
<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>
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