Skip to main content
OpenTrials
Completed

NCT Number: NCT03054051

A Mobile Phone Game to Prevent HIV Among Young Africans

This project will test the feasibility of an electronic game to prevent HIV among African preadolescents, delivered via inexpensive Android smart phones. In order to collect feasibility data for a future randomized controlled trial, this study involves the pilot-testing of the intervention with a sample of young people in Nyanza region, Kenya, where 11.4% of young women ages 15-24 are HIV-infected. This feasibility study will be carried out with the Kenya Medical Research Institute (KEMRI).

Completed

Looking for future studies?

Notify Me

Key information

About this study

This project will test the feasibility of an electronic game for preadolescents, delivered via inexpensive Android smart phones. The game is informed by socio-behavioral and pedagogical theories, evidence-based practice, and formative research on youth sexual culture in sub-Saharan Africa. It is designed to: educate young players, ages 11-14, about sexual health and HIV/AIDS; build risk-reduction skills and related self-efficacy for prevention of HIV, sexually transmitted infections (STIs), and unintended pregnancy; challenge harmful gender norms and HIV stigma; and foster dialogue with parents and caregivers.

The proposed feasibility test will be conducted in Western Kenya. Sixty preadolescents will be enrolled in the trial, 30 in the study arm and 30 in the control arm. The Kenya Medical Research Institute (KEMRI) has established community advisory boards (CABs) in Kisumu, which will be available to the proposed study.

Data collection will take place at KEMRI offices, health clinics, or in the meeting room of a local community-based organization (CBO). In addition, data on game-play will be automatically collected on mobile phones given to preadolescent study participants.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Aged 11-14 at time of recruitment
  • Resident in Nyanza region, Kenya
  • Having basic literacy in English
  • Only one child enrolled per family

Exclusion criteria

  • Aged <11 or >14 at time of recruitment
  • Not resident in Nyanza region, Kenya
  • Without basic literacy in English
  • Sibling to a child already enrolled in the study
  • Participant in formative research to inform the study

Treatment and study plan

Tumaini Mobile Phone Game

Behavioral

Tumaini is a scenario-based role-playing game application, optimized for use on low-cost Android smartphones. Participants will be invited to play the game for at least ten hours over a period of three weeks. The game is designed to: educate players about sexual health and HIV/AIDS; build risk-reduction skills and related self-efficacy for prevention of HIV/STIs and unintended pregnancy; challenge HIV stigma and harmful gender norms; and promote parent-child dialogue.

Primary outcomes

  1. Number Interested in Participating

    Time frame: Month 1

    To evaluate the feasibility of conducting a technology based intervention in a low resource area, the number of eligible individuals who were interested in participating after hearing about the study was examined. Letters were sent to 150 families inviting them to attend an informational meeting and 126 attended a meeting and were assess for eligibility.

  2. Time to Recruitment of 60 Participants

    Time frame: Month 1

    The number of days needed to recruit 60 participants.

  3. Number of Participants Lost to Follow Up

    Time frame: Duration of Study (Up to 4 Months)

    The number of participants who consented to participate but then later could not be reached prior to completing all study visits.

  4. Number of Participants Completing the Study

    Time frame: Duration of Study (Up to 4 Months)

    The number of participants who completed all study visits after providing consent are presented here.

  5. Number of Phones Returned

    Time frame: Month 2

    The phone retention rate (phones not lost during the intervention) was assessed by the number of phones returned at the end of the intervention.

  6. Number Reporting Game Was Very Fun

    Time frame: Day 17 (post-intervention)

    Game acceptability was assessed by asking participants how fun playing the game was. The number of participants reporting that the game was "very fun" are presented here.

  7. Number Reporting the Game is Valuable

    Time frame: Day 17 (post-intervention)

    The value of the game was assessed with several questions regarding how much the participants learned and how useful the information is. The number of participants reporting that they learned a lot, found the information very useful now, and found the information very useful for the future, are presented below.

  8. Number of Participants Feeling Very Safe

    Time frame: Day 17 (post-intervention)

    Personal safety associated with being in possession of the phone was assessed by the post-intervention survey. Phones provided for the intervention were set up so that all other features were blocked and only function the phone could perform was playing the game.

  9. Number of Participants Playing the Game

    Time frame: Day 17 (post-intervention)

    Participants were asked to play the game for at least one hour per day for 16 days. The number of participants who reported playing the game everyday and the number of participants who reported playing the game for an hour or more each time are presented here.

Secondary outcomes

  1. Change in Knowledge

    Time frame: Baseline, Day 17 (post-intervention), 6 Weeks Post-intervention

    Knowledge measures will be assessed via Yes/No survey questions and will address puberty, HIV, sexually transmitted infections (STIs), pregnancy, condoms, and alcohol and drugs. Knowledge was assessed with 15 items and responses are coded as 0 or 1. Total scores range from 0 to 15, with higher scores indicating increased knowledge. A positive value for the change from baseline score indicates an increase in knowledge from the baseline assessment.

  2. Change in Self-Efficacy

    Time frame: Baseline, Day 17 (post-intervention), 6 Weeks Post-intervention

    Self-efficacy was assessed via a 3-point Likert scale, and addressed self-efficacy to seek advice about puberty, sex, relationships; to communicate about protected sex; to reject peer, partner and adult pressure to engage in risk behaviors. Self-efficacy was assessed with 9 items which were scored as 0, 0.5 or 1. Total scores ranged from 0 to 9, with higher scores indicating increased self-efficacy. A positive value for the change from baseline score indicates an increase in self-efficacy since the baseline assessment.

  3. Change in Risk Assessment

    Time frame: Baseline, Day 17 (post-intervention), 6 Weeks Post-intervention

    Risk assessment was assessed via a 3-point Likert scale, and addressed perceived risk of certain risk situations/behaviors and of contracting HIV. Risk is assessed with 4 items and responses are coded as 0, 0.5 or 1. Total scores range from 0 to 4, with higher scores indicating increased risk assessment. A positive value for the change from baseline score indicates an increase in assessing risky situations as risky.

  4. Change in Behavioral Intention

    Time frame: Baseline, Day 17 (post-intervention), 6 Weeks Post-intervention

    Behavioral intention was assessed via Yes/No questions. The measure addressed intention to seek advice, to avoid risk situations, and to engage in health protective behaviors. Behavioral intention is assessed with 6 items that are scored as 0 or 1 and total scores range from 0 to 6. Higher scores in indicate more intention to partake in health protective behaviors and a positive value for the change from baseline score indicates a desirable change in intention.

  5. Change in Future Orientation

    Time frame: Baseline, Day 17 (post-intervention), 6 Weeks Post-intervention

    Future orientation was assessed via a single multiple-choice question (Yes/No/Maybe) and addressed perceived locus of control. Response is coded as 0, 0.5, or 1 and higher scores indicate greater understanding of future locus of control. A positive value for the change from baseline score indicates a desirable change in scores.

  6. Change in Perceived Social Norms

    Time frame: Baseline, Day 17 (post-intervention), 6 Weeks Post-intervention

    Perceived social norms were assessed via a 3-point Likert and addressed sex, gender, condoms, and HIV stigma. Social norms were assessed with 6 items that are scored as 0, 0.5, or 1. Total scores range from 0 to 6 with higher scores indicating perception of more desirable social norms. A positive value for the change from baseline scores indicates a desirable change.

  7. Change in Attitudes

    Time frame: Baseline, Day 17 (post-intervention), 6 Weeks Post-intervention

    Attitudes were assessed via 3-pt Likert survey questions relating to HIV stigma, condoms, sex, gender, and future orientation. Attitudes were assessed with 15 items and responses coded as 0, 0.5, or 1. Total scores ranged from 0 to 15, with higher scores indicating more desirable attitudes. A positive value for the change from baseline score indicates an increase in desirable attitudes.

Sponsors and collaborators

Lead sponsor

Emory University

Other

Collaborators

  • Kenya Medical Research Institute
  • National Institute of Mental Health (NIMH)

Registry information

Important dates

Study start
2017
Primary completion
2017
Study completion
2017
First posted
Feb 15, 2017
Registry last updated
Oct 17, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.