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Call for Life Youth ART Adherence Study

Acceptability, Effect and Cost of Mobile-health on ART Adherence Among Youths: A Mixed Methods Sequential Study in Kiryandongo

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04718974
Acronym
C4L-Youth
Enrollment
206
Registered
2021-01-22
Start date
2020-08-12
Completion date
2022-06-30
Last updated
2024-02-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

ART Adherence, HIV-1-infection, mHealth

Keywords

Youth, Adherence, ART, mobile health, resource poor setting

Brief summary

Study purpose: To assess effect of mHealth Call for life Uganda tool (CFLU) on ART adherence among youth measured by interactive voice response to daily adherence calls mapped in the database and proportion with viral suppression of copies below 1000 copies/mL. The intervention call for life Uganda (CFLU) uses IVR calls or text messages delivered via MOTECH™ based Connect for Life technology™. The calls are delivered in 4 languages (Luganda, English, Luo and Runyakitara) and the participant has to make a choice of the preferred language during registration to the system. The system offers adherence pill reminders, health message tips, visit appointment reminders and receipt of self-reported symptoms.

Detailed description

The intervention is mobile phone based IVR. However, the CLFU trial found that, it was observed that a good number of participants (50 of 256) at the urban site were not enrolled due to absence of a basic mobile phone, or had malfunctioning phone keyboards (for Poster Exhibition at the 20th International Conference on AIDS and STIs in Africa (ICASA 2019). Therefore, we shall provide a basic mobile phone to everyone in the study (SoC and intervention arm). To avoid stigma associated with a particular phone, we shall get 4 or more types of basic phones. Issues regarding simcard registration will be dealt with by the individuals. Four study questionnaires will be administered at baseline and 6-monthly until the 12-month exit visit. The questionnaires will capture: * Sociodemographic and medical history * Stigma scores * Knowledge assessment * Sexual behavior assessment * Knowledge of COVID-19 ( only at baseline) The data will be entered using REDCap. Blood for viral load will be collected at baseline and at the 6 and 12-month visit. Intervention: mHealth CFLU tool The tool capitalises on a basic mobile phone's core utilities of voice and short messaging services. The system design, development, testing and evaluation was done by Janssen and the Grameen Foundation (http://motechsuite.org/index.php/implementations). In 2015, Janssen Global Public Health Research and Development, in close collaboration with the Infectious Diseases Institute Kampala (IDI), developed Call for Life Uganda (CFLU) tailored to the needs of PLHIV in Uganda. The CFLU system follows the Health Insurance Portability and Accountability Act (HIPAA) Privacy and Security rules. While the Privacy rules deals with electronic Protected Health Information, the security rule covers administrative, physical and technical safeguards to ensure confidentiality, integrity and security of electronic protected health information. Data transaction between patient and system is encrypted when it comes to human subjects. The system is password protected, and interaction of system and patient is personalised with a secret code. The system interacts with the patient through a basic mobile phone via a keypad and with the health worker through a web-based interface. The system has options to either use interactive voice response or short message service and the user has to make a choice, get a secret pin code which ensures privacy to enduser. Screening-Enrolment procedures: All potential participants will be written on the screening log, and a screening form completed, reasons for screen failure will be documented on the screening log. Following successful screening, the participant will be referred to the Research Assistant (RA) to receive a thorough explanation of the study so and informed consent is obtained. The RA then administers the stigma questionnaire along with the sociodemographic and medical information, , HIV knowledge and sexual behaviour questionnaires. A client locater form will be completed which will help in physical contact tracing, and the participant will be registered on the enrolment log. Randomisation will follow (see details of randomisation procedure below) thereafter and the result in the sealed envelope will dictate whether the patient will be registered onto the Call for Life System for the intervention or continue with standard of care as per Ministry of Health HIV Management guidelines. Registration onto the CFLU system: Refer to Standard operating procedures on registration. However, all patients will be registered onto the electronic and hard copy of the enrolment log and a next appointment date is given to them. Finally, the lab request forms are filled and the patient sent for a blood draw. The patient returns from the lab, receives their transport refund of UGX 20,000, with a basic mobile phone (only at baseline visit, to all participants) and is allowed to go home. No intervention: Standard of care arm The Ministry of Health developed a minimum healthcare services package for PLHIV to standardize the programming, implementation and delivery of integrated HIV services in Uganda The standard of care arm is based on the Apr 2018, consolidated guidelines for prevention and treatment of HIV in Uganda (MoH, 2018), and will also follow the healthcare services package for PLHIV (Uganda. MoH, September 2014).

Interventions

OTHERmHealth call for life system/ tool using IVR ( interactive voice response)

The tool capitalises on a basic mobile phone's core utilities of voice and short messaging services. The system design, development, testing and evaluation was done by Janssen and the Grameen Foundation (http://motechsuite.org/index.php/implementations). In 2015, Janssen Global Public Health Research and Development, in close collaboration with the Infectious Diseases Institute Kampala (IDI), developed Call for Life Uganda (CFLU) tailored to the needs of PLHIV in Uganda

Sponsors

Infectious Diseases Institute, Uganda
CollaboratorOTHER
Makerere University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Intervention model description

2 groups one on intervention of Call for life mHealth with standard of care and other on standard of care only. mHealth Call for life Tool using interactive voice response

Eligibility

Sex/Gender
ALL
Age
15 Years to 24 Years
Healthy volunteers
No

Inclusion criteria

* Youth living with HIV * Documented HIV test result * ART naïve or on ART since Jun 2019

Exclusion criteria

* Youth with Hearing loss, * Youth with severe illness likely to shorten life span, * Youth in boarding schools * Inability to use a basic mobile phone

Design outcomes

Primary

MeasureTime frameDescription
• Viral Load Suppression• Viral load suppression at 6 monthsViral load suppression as per Blood draws at 6 months for those on intervention and those on standard of care arm will be used to measure viral load at these time points
Proportions Retained in Care12 monthsProportions of youth retained in care at 12 months for those on intervention in comparison to those on standard of care arm

Countries

Uganda

Participant flow

Recruitment details

Recruitment started on 12th Aug 2020. Reccruitment was from three HIV/ART clinics in Kiryandongo District

Pre-assignment details

The participants must have registered in either of the three study site. They should have been between 15-24 years and on ART for 6 months or less.

Participants by arm

ArmCount
Intervention Call for Life- mHealth Tool With Standard of Care for PLHIV
The system has options to either use interactive voice response or short message service and the user has to make a choice, get a secret pin code which ensures privacy to end user. The mHealth tool/system offers personalised pill reminder calls, health tip messages, clinic appointment reminders and remote symptom reporting mHealth call for life system/ tool using IVR ( interactive voice response): The tool capitalises on a basic mobile phone's core utilities of voice and short messaging services. The system design, development, testing and evaluation was done by Janssen and the Grameen Foundation (http://motechsuite.org/index.php/implementations). In 2015, Janssen Global Public Health Research and Development, in close collaboration with the Infectious Diseases Institute Kampala (IDI), developed Call for Life Uganda (CFLU) tailored to the needs of PLHIV in Uganda
103
Standard of Care Usual Care
Standard • Care and support for people living with HIV, and the first line ART regimen is based on the Apr 2018, consolidated guidelines for prevention and treatment of HIV in Uganda (MoH, 2018), and will also follow the healthcare services package for PLHIV including the Adult Care and Treatment Package.
103
Total206

Withdrawals & dropouts

PeriodReasonFG000FG001
Overall StudyDeath02
Overall StudyLost to Follow-up1020
Overall StudyTransferred out24

Baseline characteristics

CharacteristicStandard of Care Usual CareTotalIntervention Call for Life- mHealth Tool With Standard of Care for PLHIV
Age, Continuous22.2 years
STANDARD_DEVIATION 2.3
22.3 years
STANDARD_DEVIATION 2.1
22.5 years
STANDARD_DEVIATION 1.9
Ethnicity (NIH/OMB)
Hispanic or Latino
0 Participants0 Participants0 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
0 Participants0 Participants0 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
103 Participants206 Participants103 Participants
Region of Enrollment
Uganda
103 Participants206 Participants103 Participants
Sex: Female, Male
Female
85 Participants167 Participants82 Participants
Sex: Female, Male
Male
18 Participants39 Participants21 Participants
Viral load detection at baseline32 Participants78 Participants46 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 1032 / 103
other
Total, other adverse events
0 / 1030 / 103
serious
Total, serious adverse events
1 / 1032 / 103

Outcome results

Primary

Proportions Retained in Care

Proportions of youth retained in care at 12 months for those on intervention in comparison to those on standard of care arm

Time frame: 12 months

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Intervention Call for Life- mHealth Tool With Standard of Care for PLHIVProportions Retained in Care91 Participants
Standard of Care Usual CareProportions Retained in Care77 Participants
Primary

• Viral Load Suppression

Viral load suppression as per Blood draws at 6 months for those on intervention and those on standard of care arm will be used to measure viral load at these time points

Time frame: • Viral load suppression at 6 months

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Intervention Call for Life- mHealth Tool With Standard of Care for PLHIV• Viral Load Suppression61 Participants
Standard of Care Usual Care• Viral Load Suppression46 Participants
Primary

• Viral Load Suppression

Viral load suppression as per Blood draws at 12 months for those on intervention and those on standard of care arm will be used to measure viral load status at these time points

Time frame: • Viral load suppression at 12 months

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Intervention Call for Life- mHealth Tool With Standard of Care for PLHIV• Viral Load Suppression67 Participants
Standard of Care Usual Care• Viral Load Suppression40 Participants

Source: ClinicalTrials.gov · Data processed: Feb 5, 2026