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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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12 December 2020 |
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Main ID: |
NCT03045809 |
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Date of registration:
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02/02/2017 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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Women's Improvement of Sexual Health (WISH) Demonstration Project
WISH |
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Scientific title:
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Improving HIV Prevention and Sexual and Reproductive Health Care in High Risk Women in Rwanda Using Lessons Learnt From Previous Rinda Ubuzima Projects |
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Date of first enrolment:
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July 5, 2016 |
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Target sample size:
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705 |
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Recruitment status: |
Completed |
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URL:
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https://clinicaltrials.gov/show/NCT03045809 |
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Study type:
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Observational |
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Study design:
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Phase:
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Countries of recruitment
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Rwanda
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Contacts
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Name:
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Janneke van de Wijgert, MD PhD MPH |
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Address:
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Telephone:
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Email:
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Affiliation:
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University of Liverpool |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- Female, at least 18 years old (no upper age limit)
- At high risk of HIV/STIs, defined as having had more than one sexual partner in the
last 12 months OR having been treated for an STI in the last 12 months
- Willing and able to provide written informed consent.
Exclusion Criteria:
- Already participated in this study before (each woman can only participate once)
- Participating in another health intervention study
- For any other reason as judged by the Principal Investigator (these reasons will be
recorded)
Age minimum:
18 Years
Age maximum:
N/A
Gender:
Female
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Health Condition(s) or Problem(s) studied
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Bacterial Vaginosis
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Vaginal Candidiasis
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Sexually Transmitted Disease
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Urinary Tract Infections
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Intervention(s)
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Diagnostic Test: Urogenital infection point-of-care tests
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Primary Outcome(s)
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Feasibility of Integrating Point-of-care Testing (Client Satisfaction Surveys)
[Time Frame: Each client satisfaction survey was conducted at a main visit and lasted up to 30 min.]
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Performance of Syndromic Management With or Without Integration of Point-of-care Tests
[Time Frame: Each participant was assessed at one main study visit, which lasted up to 4 hours.]
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Feasibility of Integrating Point-of-care Testing (Monitoring & Evaluation Indicators)
[Time Frame: Each participant was assessed at one main study visit, which lasted up to 4 hours.]
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Secondary ID(s)
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UoL001208
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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