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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: |
NCT02918838 |
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Date of registration:
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14/09/2016 |
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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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Supporting Adolescents to Adhere - an Intervention Using Airtime Rewards Allocated by a Prize Drawing
SATA |
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Scientific title:
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Supporting Adolescents to Adhere - an Intervention Using Airtime Rewards Allocated by a Prize Drawing |
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Date of first enrolment:
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August 2016 |
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Target sample size:
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216 |
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Recruitment status: |
Completed |
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URL:
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https://clinicaltrials.gov/show/NCT02918838 |
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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: Treatment. Masking: Single (Outcomes Assessor).
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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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Sebastian Linnemayr, 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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RAND |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- have been in HIV care at the clinic for at least three months
- are currently taking HIV-related medication (ART or co-trimoxazole)
- either own a phone or have regular access to one
- intend to stay at the clinic for the study period
- are not in boarding school (where phones are forbidden)
Exclusion Criteria:
- does not speak or understand either English or Luganda
Age minimum:
16 Years
Age maximum:
25 Years
Gender:
All
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Health Condition(s) or Problem(s) studied
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Human Immunodeficiency Virus
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Intervention(s)
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Behavioral: Fixed Adherence Group
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Behavioral: Control Group
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Behavioral: Own Adherence Group
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Primary Outcome(s)
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Medication adherence rates using electronically monitored adherence (MEMS cap) data
[Time Frame: 9 months after enrollment]
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Secondary Outcome(s)
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Fraction of clients displaying adherence of 90% or more
[Time Frame: 9 months after enrollment]
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Viral load assays
[Time Frame: 9 months after enrollment]
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Indicator for treatment interruptions of more than 48 hours
[Time Frame: 9 months after enrollment]
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Secondary ID(s)
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3R01HD074925-04S1
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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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