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Note: This record shows only the 20 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.
Register: PACTR
Last refreshed on: 29 April 2013
Main ID:  PACTR201105000299318
Date of registration: 16/05/2011
Primary sponsor: Canadian International Development Agency (CIDA)
Public title: Using mobile-phone based text messages to improve retention of patients initiating antiretroviral therapy in South Africa
Scientific title: Using mobile-phone based text messages to improve retention of patients initiating antiretroviral therapy in South Africa
Date of first enrolment: 2011-06-01
Target sample size: 1200
Recruitment status: Not yet recruiting
URL:  HTTP://www.pactr.org/ATMWeb/appmanager/atm/atmregistry?da=true&tno=PACTR201105000299318
Study type:  interventional
Study design:  Parallel: different groups receive different interventions at same time during study,
Randomised,
Permuted block randomisation ,
Allocation will be determined by software package - system allocated patients to intervention arm,
 
Countries of recruitment
South Africa
Contacts
Name: Leya  Hassanally
Address:  1st Floor CPUT BARC Building Cnr Brandweer/Waterloo St 8001 Cape Town South Africa
Telephone: 27 (0)21 469-1111
Email: Leya@cell-life.org
Affiliation:  Lead Researcher and Co-Principal Investigator
Name: Sarah  Brown
Address:  1st Floor CPUT BARC Building Cnr Brandweer/Waterloo St 8001 Cape Town South Africa
Telephone: 27 (0)21 469-1111
Email: Sarah@cell-life.org
Affiliation:  Project Manager and Co-Principal Investigator
Key inclusion & exclusion criteria
Inclusion criteria: Patients who are 18 years of age or older.
Patients who are initiating ART.
Patients who own or have access to a mobile phone with functional text message features.
Patients who can receive text messages.
Patients who can read text messages.
Patients who agree to continue their ART at the site at which they were initiated for 12 months. In other words, the patient will not be down referred to a local community clinic during the study.

Exclusion criteria: Patients who reside in an area where there is no mobile network reception.
Patients who plan to relocate away from the area or transfer to another antiretroviral treatment facility during the next 12 months.
Patients who are enrolled in other concurrent research studies designed to investigate the effect of mobile-phone based text message reminders to improve retention in treatment.
Patients who belong to a household within which another individual has already enrolled for the study.


Age minimum: 18 Year
Age maximum: 100 Year
Gender: Both
Health Condition(s) or Problem(s) studied

HIV/AIDS
null
Intervention(s)
Primary Outcome(s)
Retention
Treatment Interruptions
Secondary Outcome(s)
awareness of possible adverse effects and toxicity
Clinical outcome: HIV-1 RNA viral load and CD4 T-lymphocyte count
commitment to treatment
disclosure of HIV status
experienced stigma and depression
interpersonal relationships
knowledge of difficulties experienced during ART initiation
lifestyle changes for improved health outcomes
optimistic self-beliefs about health benefits of ART
patient medication self-efficacy
perceived social support
Secondary ID(s)
Source(s) of Monetary Support
Canadian International Development Agency (CIDA)
Secondary Sponsor(s)
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