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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: |
NCT02729337 |
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Date of registration:
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15/03/2016 |
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Prospective Registration:
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Yes |
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Primary sponsor: |
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Public title:
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Affecting the Epidemiology of HIV in Uganda
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Scientific title:
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Affecting the Epidemiology of HIV in Uganda Through Older Adolescents |
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Date of first enrolment:
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December 6, 2017 |
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Target sample size:
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203 |
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Recruitment status: |
Completed |
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URL:
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https://clinicaltrials.gov/show/NCT02729337 |
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Study type:
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Interventional |
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Study design:
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Allocation: Randomized. Intervention model: Parallel Assignment. Primary purpose: Prevention. Masking: Single (Participant).
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Phase:
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N/A
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Countries of recruitment
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Uganda
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Contacts
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Name:
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Michele Ybarra, MPH PHD |
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Address:
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Telephone:
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Email:
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Affiliation:
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Center for Innovative Public Health Research |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- living in Uganda
- aged 18-22 years
- able to read English
- exclusive owner of a cell phone
- using text messaging for at least 6 months
- intended to have the same phone number or the next six months
- able to access the Internet (to complete online surveys)
- able to provide informed consent
Exclusion Criteria:
- no other exclusion criteria will be applied
Age minimum:
18 Years
Age maximum:
22 Years
Gender:
All
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Health Condition(s) or Problem(s) studied
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HIV
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Sexual Abstinence
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Contraceptive Usage
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Intervention(s)
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Behavioral: ITG (In This Together)
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Primary Outcome(s)
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Program acceptability as assessed by a scale created for the RCT
[Time Frame: At intervention end, 6-weeks post baseline]
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Program feasibility: Recruitment
[Time Frame: 24 weeks]
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Program feasibility: Retention
[Time Frame: Through study completion, an average of 6 weeks]
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Secondary Outcome(s)
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Percent of participants who have gotten an HIV test as assessed by self-report
[Time Frame: At intervention end, 6-weeks post baseline]
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Percent of participants reporting abstinence as assessed by self-report
[Time Frame: At intervention end, 6-weeks post baseline]
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Percent of participants reporting condom use during sex as assessed by self-report
[Time Frame: At intervention end, 6-weeks post baseline]
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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