Effectiveness of Clinic-Based Patient-Led Human Papilloma-virus DNA Self-Sampling Among HIV-Infected Women in Uganda.
Not Applicable
- Conditions
- CancerHIV/AIDSHumanpapilloma virus
- Registration Number
- PACTR202310623752472
- Lead Sponsor
- niversity of KwaZulu Natal
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 75
Inclusion Criteria
The study team approached and enrolled all HIV-infected women;
•Not pregnant
•Not in menstrual periods
•Aged 25 to 49 years who have never been screened
•Not screened within the last year (those who have screened for more than 1 year with normal results)
•Have abnormal screening results
•Attending the HIV clinic
•Have provided informed consent to them to participate in the study.
Exclusion Criteria
All women who were critically ill and declined to participate in the study were excluded.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Continuation rate for HPV self-sampling.
- Secondary Outcome Measures
Name Time Method Cost-effectiveness of clinic-based HPV self-sampling