HIV InfectionsMOTIVESNCT03144336
Using Mobile Technology and Incentives With Men Who Have Sex With Men and Transgender Women for HIV Prevention
A study testing Information provision, Weekly quizzes and Rewards for testing HIV-negative in people with HIV Infections and HIV, run by RAND at 1 site in United States.
Trial summary
This project called Mobile Technology and Incentives (MOTIVES) aims to increase engagement with HIV prevention information and improve testing frequency among Latino/a men who have sex with men (MSM) and transgender women (TGW). Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- HIV Infections, HIV
- What is being tested?
- Information provision, Weekly quizzes and Rewards for testing HIV-negative
- Type of treatment
- Lifestyle or therapy programme
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 217 participants
- Where
- 1 siteUnited States
- Study dates
- 24 May 2017to 23 Aug 2019
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- own or have regular access to a smartphone
- self-identify as a Latino
- fluent in English or Spanish
- able to provide contact information for at least three tracking mechanisms (e.g., cell phone, email, address, friend's contact)
- HIV-negative
Who cannot join
- -
Trial locations and contacts
1 site in 1 country.
United States1 site
Bienestar Human Services, Inc.
Los Angeles, California, 90022
About this study
Official title: Using Mobile Technology and Incentives With Men Who Have Sex With Men and Transgender Women for HIV Prevention (MOTIVES)
This project called Mobile Technology and Incentives (MOTIVES) aims to increase engagement with HIV prevention information and improve testing frequency among Latino/a men who have sex with men (MSM) and transgender women (TGW). Its primary goal is to develop and test the feasibility and acceptability of an HIV prevention intervention that uses text messages in combination with prizes to improve HIV prevention information retention and HIV testing frequency. The project will be conducted in collaboration with Bienestar Human Services, Inc. (Bienestar) in Los Angeles County. Phase 1 consists of formative research (focus groups n=9) with MSM (n=52) and TGW (n=39) to complement the previously collected pilot data (2014-2015) to finalize the planned intervention. In Phase 2, the intervention will be piloted among 5 individuals, implemented, and tested in a small, randomized controlled trial (RCT) among 200 Latino MSM and TGW from Bienestar's HIV testing sites. Interested individuals will be screened for eligibility upon testing HIV-negative (those testing positive will be linked to HIV services as required by Bienestar's standard of care). Eligible participants will be randomized into either the intervention or control group that will both receive study information weekly and will be invited to get tested for HIV every three months. Participants in the intervention group will be able to accumulate rewards points for correctly answering weekly quizzes regarding the HIV prevention information; these reward incentives aim to encourage retention in the study and improve HIV prevention knowledge engagement and recollection. Every three months those in the intervention group can win a prize based on testing HIV-negative at least once during that time period. The chance of winning will increase based on the number of reward points a participant accumulates by correctly answering questions on the weekly quizzes. The primary outcome measures will include HIV-preventive knowledge and frequency of HIV testing (at least once every 3 months). In Phase 3 of the study, the investigators will conduct 6 focus groups with approximately 5-8 participants each among MSM (n=3) and TGW (n=1) study participants, testing site staff (n=1), and administrative staff (n=1) to identify implementation challenges and areas for improvement; and estimate mission-critical design parameters with point and confidence interval estimates to inform a subsequent, fully-powered R01 application.
Read the detailed description
This project entails a 3-phase mobile technology based and behavioral economics supported HIV prevention intervention - called Mobile Technology and Incentives (MOTIVES) - to increase engagement with HIV prevention information and improve testing frequency among Latino men who have sex with men (MSM) and transgender women (TGW). The study is conducted in collaboration with Bienestar Human Services, Inc. (Bienestar); a non-profit community-based service organization established in 1989 with sites located across Los Angeles County that primarily serves Latino populations. Specific Aim 1 included focus groups with MSM and TGW to finalize the planned intervention based on the insights from a preliminary study. Specific Aim 2 will enroll 200 HIV-negative MSM and TGW in a 12-month, two-arm randomized controlled trial (RCT). Those in the intervention group will receive weekly text messages with HIV prevention information and can win reward points for correctly answering weekly quizzes to keep them engaged and improve their retention of the HIV prevention information. Those who continue to test negative for HIV at least once every three months can enter a prize drawing to win prizes, with larger chances for those correctly answering the weekly quizzes. The control group will receive the same HIV prevention information but without the incentives. The secondary outcomes include sexual risk behaviors and HIV infection. Specific Aim 3 includes 6 exit focus groups (with 5-8 participants per group) to evaluate areas for study improvement and estimate parameters for future scale up. The Specific Aims are to 1) develop MOTIVES and finalize the weekly text message information content and the types of incentives; 2) implement and evaluate the impact of MOTIVES; and 3) evaluate areas of improvement for MOTIVES through focus groups and estimate mission-critical design parameters with point and confidence interval estimates for a subsequent, fully-powered R01 application.
SUMMARY OF PHASE 1 Phase 1 developed the intervention parameters to inform the implementation of MOTIVES. The focus groups built on the preliminary study information and gathered data regarding specific barriers to receiving HIV prevention information, frequent testing, type of information, incentive and prize drawing parameters from MSM and TGW clients. The focus groups took between 60 to 90 minutes and were conducted by Dr. MacCarthy and Study Coordinator, Joanna Barreras in English or Spanish as preferred by the participants. Clients were provided a copy of the informed consent and received an overview of the study, the purpose of Phase 1, procedures, potential risks and discomforts, anticipated benefits, alternatives to participation, payment for participation, privacy and confidentiality. All focus groups were digitally recorded and translated into English when needed. All focus groups content was synthesized to produce summary memos on specific topics describing each theme, presenting segments of text as exemplars.
SUMMARY OF PHASE 2 Phase 2 will conduct a small RCT among 200 Bienestar clients that will be piloted with five participants. Quantitative data on primary (e.g., HIV knowledge and frequency of testing behavior) and secondary outcomes (e.g., self-reported sexual risk behavior - to determine how well participants translated their HIV prevention knowledge into behavior over the study period, and HIV status) will be collected.
Clients who express interest and are eligible will undergo the consent process. At enrollment, several steps will be taken to increase the confidentiality of participants related to text message communication. For example, HIV testers will instruct participants how to maintain privacy on their device, and delete SMS messages from their mobile device. At recruitment, HIV testers will ask the participant to save the number from which the messages will be sentas 'MOTIVES' so that the respondent easily recognizes the sender without increasing the chance of accidental disclosure of study participation. Further, participants will be reminded that they will receive texts on the same day every week (e.g., Wednesday and Friday) and at the same times of the week (e.g., 2 pm PST) to help them anticipate the arrival of study-related communication. The text message database will be secured by password protection, anonymized data, and managed onsite. The participant will then participate the baseline survey (details of the survey described later). The participant will then be randomized into either intervention or control group. The randomization of TGW will be performed separately from MSM to ensure equal distribution of TGW in both arms (approximately 90 MSM and 10 TGW in each arm). This is important because our pilot data suggests TGW experience much higher levels of risk and vulnerability to HIV compared to MSM and will represent a smaller percentage of the overall study population.
Follow-up surveys at 6 months and 12 months after enrollment: Our pilot data suggests that most participants will have access to the Internet and accommodations will be made for participants who are not able to access the Internet. The month 12 follow-up survey will have a reduced number of questions to complete. Participants will be asked to complete their final survey 12 months after enrollment. Thus the final survey will be conducted when the intervention period has ended and therefore completing the questions at a Bienestar testing location will not confound the outcome of interest. Those who do not complete their HIV test for that period can complete the final survey at Bienestar. The survey measures used have been successfully applied in our prior research among MSM and TGW. All measures described below will be assessed at baseline and 12 months, whereas a select few will be assessed at month six to keep the survey burden of the online surveys at the interim month survey low.
Participants will be invited to return to one of the Bienestar testing sites at least once every three months to be re-tested for HIV (for the intervention group, this will be the eligibility criterion for entering the prize drawings). The participants will received a text message reminder 2.5 months after their last HIV test to get their HIV test again and remind them to make sure the study staff knows that they have completed their HIV test and that they continue to be negative to qualify for additional gift cards. Individuals who test HIV positive will be given referrals to Bienestar's HIV linkage to care programs.
Text messaging that addresses the unique needs of Latino MSM and TGW clients will be sent in Spanish or English (based on the preference of the participant) weekly. Based on feedback from our focus groups, the initial information will likely be sent on Wednesday and then followed up on Friday. The study team will include ways to access additional information, if participants wish to do so after receiving a text message, by sending an additional link, as well as a phone number that the participant can call. The phone number will connect clients to study staff that have the same information available via the link and they will be prepared to relay this information over the phone. The structure of these weekly information messages could be of the following format: "Hi [name of participant], did you know that [information content]? Use this link [hyperlink] or call [number] for more information." These messages will be sent to both control and intervention groups.
The analysis for phase two aims to obtain estimates of the intervention's acceptance and feasibility by determining enrollment and retention rates in the study. This will be determined by using the number of clients screening positive for eligibility in the survey, the number of clients enrolling in the study per month, and percentage of enrolled clients who respond to the weekly quizzes and are eligible to participate in the testing-based prize drawings, and participants retained in the study. The focus groups in Phase 3 will also provide valuable feedback about the acceptability of the program to clients and clinic personnel.
A brief questionnaire module for participants in the intervention group will assess their experience at the last assessment. Items will assess level of satisfaction with the intervention, perception of its fairness and transparency, whether they perceive the intervention to have influenced their behavior and which HIV prevention strategy that they learned during the intervention have they been most likely to employ. Participants will be asked to indicate whether more or less frequent awarding of prizes or a different prize value would have influenced their adherence to more frequent HIV testing and other behaviors of interest. These items will use a 5-point Likert scale to rate level of agreement with statements. Finally, participants will be asked open-ended questions to elicit feedback on aspects of the program that they liked or did not like, and any suggestions for how the program could be improved.
SUMMARY OF PHASE 3 In Phase 3 of the study, focus groups discussion will identify implementation challenges and areas for improvement in preparation for a R01 submission for an intervention at scale. There will be three types of focus groups: (1) MSM and TGW clients from the intervention group and (2) testing staff and administrators. Focus groups will separately be run for MSM (n=3) and TGW (n=1) clients to broadly assess their experience participating in the intervention and for testing staff (n=1) to examine perception of study procedures, and identify areas for improvement. All of the groups will discuss how to best adapt the study for future scale up and implementation. Specially, the client focus groups will cover barriers and facilitators to obtaining HIV prevention information through the intervention messaging and ask about how information receipt did (or did not) translate into healthy behavior change. Ultimately these findings will guide the scale up and implementation of a large scale R01 RCT.
- Conditions
- HIV Infections, HIV
- Being tested
- Information provision, Weekly quizzes, Rewards for testing HIV-negative
- Medical subject headings
- HIV Infections
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Information provisionBehavioural
All study participants will receive weekly messages with HIV prevention information.
Weekly quizzesBehavioural
Those in the intervention group receive a weekly quiz by text message that gains them points increasing their chances of winning a prize if answered correctly
Rewards for testing HIV-negativeBehavioural
Those in the intervention group are entered into a prize drawing if they test HIV-negative at least once in a three-month period.
| Study group | Role | What they receive |
|---|---|---|
| Intervention group | Experimental | Participants in the intervention group will be able to accumulate rewards points for correctly answering weekly quizzes regarding the HIV prevention information; these reward incentives aim to encourage retention in the study and improve HIV prevention knowledge engagement and recollection.
Intervention 'Rewards for testing HIV-negative' Every three months those in the intervention group can win a prize based on testing HIV-negative at least once during that time period. The chance of winning will increase based on the number of reward points a participant accumulates by correctly answering questions on the weekly quizzes. Receives: Behavioral: Information provision; Behavioral: Weekly quizzes; Behavioral: Rewards for testing HIV-negative |
| Control group | Active comparator | Intervention: Information provision: Participants in the control group will receive weekly information by SMS to encourage retention in the study and improve HIV prevention knowledge engagement and recollection. They are encouraged to come to the clinic every three months to test for HIV but do not receive any incentives for answering messages or for the HIV tests. Receives: Behavioral: Information provision |
What is being measured
The primary outcome is the main question the study is designed to answer.
HIV knowledge
HIV knowledge using the 18 items in Carey, M. P., \& Schroder, K. E. E. (2002). Development and psychometric evaluation of the brief HIV knowledge questionnaire (HIV-KQ-18). AIDS Education and Prevention, 14, 174-184.
Measured: 12 months
HIV testing frequency
Whether a participant tests HIV-negative within a given 3-month window
Measured: 12 months
Secondary outcomes (2)
HIV seroconversion
Participant testing HIV-positive
Measured: 12 months
Sexual risk behavior
Self-reported sexual behaviors
Measured: 12 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted8 May 2017
- Study start24 May 2017
- Primary completion23 Aug 2019
- Study completion23 Aug 2019
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (2)Papers the sponsor has linked to this study.
- Other trials for HIV InfectionsStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Double blind
- Who is masked
- Investigator, Outcomes assessor
- Enrolment
- 217 participants (actual)
Sponsor and investigators
- Lead sponsor
- RAND
- Sponsor type
- University, hospital or other
- Collaborators
- Columbia University, Bienestar Human Services, Inc.
- Responsible party
- Principal investigator, Sebastian Linnemayr, RAND
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT03144336
- Sponsor's protocol ID
- RAND
- Acronym
- MOTIVES
- Status last verified
- Sep 2019
- First submitted
- 27 Apr 2017
- Last updated
- 10 Sep 2019
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Undecided
Publications
MacCarthy S, Mendoza-Graf A, Wagner Z, L Barreras J, Kim A, Giguere R, Carballo-Dieguez A, Linnemayr S. The acceptability and feasibility of a pilot study examining the impact of a mobile technology-based intervention informed by behavioral economics to improve HIV knowledge and testing frequency among Latinx sexual minority men and transgender women. BMC Public Health. 2021 Feb 12;21(1):341. doi: 10.1186/s12889-021-10335-5.
PubMed 33579242Linnemayr S, MacCarthy S, Kim A, Giguere R, Carballo-Dieguez A, Barreras JL. Behavioral economics-based incentives supported by mobile technology on HIV knowledge and testing frequency among Latino/a men who have sex with men and transgender women: Protocol for a randomized pilot study to test intervention feasibility and acceptability. Trials. 2018 Oct 5;19(1):540. doi: 10.1186/s13063-018-2867-1.
PubMed 30290851
Study at a glance
From the registry record, last updated by the sponsor on 10 Sep 2019. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Using Mobile Technology and Incentives With Men Who Have Sex With Men and Transgender Women for HIV Prevention (MOTIVES)
- ClinicalTrials.gov ID
- NCT03144336
- Acronym / sponsor ID
- MOTIVES / RAND
- Conditions
- HIV Infections, HIV
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 217 participants (actual)
- Lead sponsor
- RANDUniversity, hospital or other
- Collaborators
- Columbia University, Bienestar Human Services, Inc.
- Study start
- 24 May 2017 (actual)
- Primary completion
- 23 Aug 2019 (actual)
- Study completion
- 23 Aug 2019 (actual)
- First posted
- 8 May 2017 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This project called Mobile Technology and Incentives (MOTIVES) aims to increase engagement with HIV prevention information and improve testing frequency among Latino/a men who have sex with men (MSM) and transgender women (TGW). Its primary goal is to develop and test the feasibility and acceptability of an HIV prevention intervention that uses text messages in combination with prizes to improve HIV prevention information retention and HIV testing frequency. The project will be conducted in collaboration with Bienestar Human Services, Inc. (Bienestar) in Los Angeles County. Phase 1 consists of formative research (focus groups n=9) with MSM (n=52) and TGW (n=39) to complement the previously collected pilot data (2014-2015) to finalize the planned intervention. In Phase 2, the intervention will be piloted among 5 individuals, implemented, and tested in a small, randomized controlled trial (RCT) among 200 Latino MSM and TGW from Bienestar's HIV testing sites. Interested individuals will be screened for eligibility upon testing HIV-negative (those testing positive will be linked to HIV services as required by Bienestar's standard of care). Eligible participants will be randomized into either the intervention or control group that will both receive study information weekly and will be invited to get tested for HIV every three months. Participants in the intervention group will be able to accumulate rewards points for correctly answering weekly quizzes regarding the HIV prevention information; these reward incentives aim to encourage retention in the study and improve HIV prevention knowledge engagement and recollection. Every three months those in the intervention group can win a prize based on testing HIV-negative at least once during that time period. The chance of winning will increase based on the number of reward points a participant accumulates by correctly answering questions on the weekly quizzes. The primary outcome measures will include HIV-preventive knowledge and frequency of HIV testing (at least once every 3 months). In Phase 3 of the study, the investigators will conduct 6 focus groups with approximately 5-8 participants each among MSM (n=3) and TGW (n=1) study participants, testing site staff (n=1), and administrative staff (n=1) to identify implementation challenges and areas for improvement; and estimate mission-critical design parameters with point and confidence interval estimates to inform a subsequent, fully-powered R01 application.
Detailed description
This project entails a 3-phase mobile technology based and behavioral economics supported HIV prevention intervention - called Mobile Technology and Incentives (MOTIVES) - to increase engagement with HIV prevention information and improve testing frequency among Latino men who have sex with men (MSM) and transgender women (TGW). The study is conducted in collaboration with Bienestar Human Services, Inc. (Bienestar); a non-profit community-based service organization established in 1989 with sites located across Los Angeles County that primarily serves Latino populations. Specific Aim 1 included focus groups with MSM and TGW to finalize the planned intervention based on the insights from a preliminary study. Specific Aim 2 will enroll 200 HIV-negative MSM and TGW in a 12-month, two-arm randomized controlled trial (RCT). Those in the intervention group will receive weekly text messages with HIV prevention information and can win reward points for correctly answering weekly quizzes to keep them engaged and improve their retention of the HIV prevention information. Those who continue to test negative for HIV at least once every three months can enter a prize drawing to win prizes, with larger chances for those correctly answering the weekly quizzes. The control group will receive the same HIV prevention information but without the incentives. The secondary outcomes include sexual risk behaviors and HIV infection. Specific Aim 3 includes 6 exit focus groups (with 5-8 participants per group) to evaluate areas for study improvement and estimate parameters for future scale up. The Specific Aims are to 1) develop MOTIVES and finalize the weekly text message information content and the types of incentives; 2) implement and evaluate the impact of MOTIVES; and 3) evaluate areas of improvement for MOTIVES through focus groups and estimate mission-critical design parameters with point and confidence interval estimates for a subsequent, fully-powered R01 application.
SUMMARY OF PHASE 1 Phase 1 developed the intervention parameters to inform the implementation of MOTIVES. The focus groups built on the preliminary study information and gathered data regarding specific barriers to receiving HIV prevention information, frequent testing, type of information, incentive and prize drawing parameters from MSM and TGW clients. The focus groups took between 60 to 90 minutes and were conducted by Dr. MacCarthy and Study Coordinator, Joanna Barreras in English or Spanish as preferred by the participants. Clients were provided a copy of the informed consent and received an overview of the study, the purpose of Phase 1, procedures, potential risks and discomforts, anticipated benefits, alternatives to participation, payment for participation, privacy and confidentiality. All focus groups were digitally recorded and translated into English when needed. All focus groups content was synthesized to produce summary memos on specific topics describing each theme, presenting segments of text as exemplars.
SUMMARY OF PHASE 2 Phase 2 will conduct a small RCT among 200 Bienestar clients that will be piloted with five participants. Quantitative data on primary (e.g., HIV knowledge and frequency of testing behavior) and secondary outcomes (e.g., self-reported sexual risk behavior - to determine how well participants translated their HIV prevention knowledge into behavior over the study period, and HIV status) will be collected.
Clients who express interest and are eligible will undergo the consent process. At enrollment, several steps will be taken to increase the confidentiality of participants related to text message communication. For example, HIV testers will instruct participants how to maintain privacy on their device, and delete SMS messages from their mobile device. At recruitment, HIV testers will ask the participant to save the number from which the messages will be sentas 'MOTIVES' so that the respondent easily recognizes the sender without increasing the chance of accidental disclosure of study participation. Further, participants will be reminded that they will receive texts on the same day every week (e.g., Wednesday and Friday) and at the same times of the week (e.g., 2 pm PST) to help them anticipate the arrival of study-related communication. The text message database will be secured by password protection, anonymized data, and managed onsite. The participant will then participate the baseline survey (details of the survey described later). The participant will then be randomized into either intervention or control group. The randomization of TGW will be performed separately from MSM to ensure equal distribution of TGW in both arms (approximately 90 MSM and 10 TGW in each arm). This is important because our pilot data suggests TGW experience much higher levels of risk and vulnerability to HIV compared to MSM and will represent a smaller percentage of the overall study population.
Follow-up surveys at 6 months and 12 months after enrollment: Our pilot data suggests that most participants will have access to the Internet and accommodations will be made for participants who are not able to access the Internet. The month 12 follow-up survey will have a reduced number of questions to complete. Participants will be asked to complete their final survey 12 months after enrollment. Thus the final survey will be conducted when the intervention period has ended and therefore completing the questions at a Bienestar testing location will not confound the outcome of interest. Those who do not complete their HIV test for that period can complete the final survey at Bienestar. The survey measures used have been successfully applied in our prior research among MSM and TGW. All measures described below will be assessed at baseline and 12 months, whereas a select few will be assessed at month six to keep the survey burden of the online surveys at the interim month survey low.
Participants will be invited to return to one of the Bienestar testing sites at least once every three months to be re-tested for HIV (for the intervention group, this will be the eligibility criterion for entering the prize drawings). The participants will received a text message reminder 2.5 months after their last HIV test to get their HIV test again and remind them to make sure the study staff knows that they have completed their HIV test and that they continue to be negative to qualify for additional gift cards. Individuals who test HIV positive will be given referrals to Bienestar's HIV linkage to care programs.
Text messaging that addresses the unique needs of Latino MSM and TGW clients will be sent in Spanish or English (based on the preference of the participant) weekly. Based on feedback from our focus groups, the initial information will likely be sent on Wednesday and then followed up on Friday. The study team will include ways to access additional information, if participants wish to do so after receiving a text message, by sending an additional link, as well as a phone number that the participant can call. The phone number will connect clients to study staff that have the same information available via the link and they will be prepared to relay this information over the phone. The structure of these weekly information messages could be of the following format: "Hi [name of participant], did you know that [information content]? Use this link [hyperlink] or call [number] for more information." These messages will be sent to both control and intervention groups.
The analysis for phase two aims to obtain estimates of the intervention's acceptance and feasibility by determining enrollment and retention rates in the study. This will be determined by using the number of clients screening positive for eligibility in the survey, the number of clients enrolling in the study per month, and percentage of enrolled clients who respond to the weekly quizzes and are eligible to participate in the testing-based prize drawings, and participants retained in the study. The focus groups in Phase 3 will also provide valuable feedback about the acceptability of the program to clients and clinic personnel.
A brief questionnaire module for participants in the intervention group will assess their experience at the last assessment. Items will assess level of satisfaction with the intervention, perception of its fairness and transparency, whether they perceive the intervention to have influenced their behavior and which HIV prevention strategy that they learned during the intervention have they been most likely to employ. Participants will be asked to indicate whether more or less frequent awarding of prizes or a different prize value would have influenced their adherence to more frequent HIV testing and other behaviors of interest. These items will use a 5-point Likert scale to rate level of agreement with statements. Finally, participants will be asked open-ended questions to elicit feedback on aspects of the program that they liked or did not like, and any suggestions for how the program could be improved.
SUMMARY OF PHASE 3 In Phase 3 of the study, focus groups discussion will identify implementation challenges and areas for improvement in preparation for a R01 submission for an intervention at scale. There will be three types of focus groups: (1) MSM and TGW clients from the intervention group and (2) testing staff and administrators. Focus groups will separately be run for MSM (n=3) and TGW (n=1) clients to broadly assess their experience participating in the intervention and for testing staff (n=1) to examine perception of study procedures, and identify areas for improvement. All of the groups will discuss how to best adapt the study for future scale up and implementation. Specially, the client focus groups will cover barriers and facilitators to obtaining HIV prevention information through the intervention messaging and ask about how information receipt did (or did not) translate into healthy behavior change. Ultimately these findings will guide the scale up and implementation of a large scale R01 RCT.
Study design
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Double blind (investigator, outcomes assessor)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Intervention group | Experimental | Behavioral: Information provision, Behavioral: Weekly quizzes, Behavioral: Rewards for testing HIV-negativeParticipants in the intervention group will be able to accumulate rewards points for correctly answering weekly quizzes regarding the HIV prevention information; these reward incentives aim to encourage retention in the study and improve HIV prevention knowledge engagement and recollection. Intervention 'Rewards for testing HIV-negative' Every three months those in the intervention group can win a prize based on testing HIV-negative at least once during that time period. The chance of winning will increase based on the number of reward points a participant accumulates by correctly answering questions on the weekly quizzes. |
| Control group | Active comparator | Behavioral: Information provisionIntervention: Information provision: Participants in the control group will receive weekly information by SMS to encourage retention in the study and improve HIV prevention knowledge engagement and recollection. They are encouraged to come to the clinic every three months to test for HIV but do not receive any incentives for answering messages or for the HIV tests. |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (5 listed)
- own or have regular access to a smartphone
- self-identify as a Latino
- fluent in English or Spanish
- able to provide contact information for at least three tracking mechanisms (e.g., cell phone, email, address, friend's contact)
- HIV-negative
Key exclusion criteria (1 listed)
- -
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Information provisionAll study participants will receive weekly messages with HIV prevention information. | Behavioural | Control group, Intervention group |
| Weekly quizzesThose in the intervention group receive a weekly quiz by text message that gains them points increasing their chances of winning a prize if answered correctly | Behavioural | Intervention group |
| Rewards for testing HIV-negativeThose in the intervention group are entered into a prize drawing if they test HIV-negative at least once in a three-month period. | Behavioural | Intervention group |
Primary outcome
HIV knowledge
Time frame: 12 months
HIV knowledge using the 18 items in Carey, M. P., \& Schroder, K. E. E. (2002). Development and psychometric evaluation of the brief HIV knowledge questionnaire (HIV-KQ-18). AIDS Education and Prevention, 14, 174-184.
HIV testing frequency
Time frame: 12 months
Whether a participant tests HIV-negative within a given 3-month window
2 secondary outcomes
HIV seroconversion
Time frame: 12 months
Sexual risk behavior
Time frame: 12 months
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 10 Sep 2019.
- Derived from this study: PubMed 33579242MacCarthy S, Mendoza-Graf A, Wagner Z, L Barreras J, Kim A, Giguere R, Carballo-Dieguez A, Linnemayr S. The acceptability and feasibility of a pilot study examining the impact of a mobile technology-based intervention informed by behavioral economics to improve HIV knowledge and testing frequency among Latinx sexual minority men and transgender women. BMC Public Health. 2021 Feb 12;21(1):341. doi: 10.1186/s12889-021-10335-5.
- Derived from this study: PubMed 30290851Linnemayr S, MacCarthy S, Kim A, Giguere R, Carballo-Dieguez A, Barreras JL. Behavioral economics-based incentives supported by mobile technology on HIV knowledge and testing frequency among Latino/a men who have sex with men and transgender women: Protocol for a randomized pilot study to test intervention feasibility and acceptability. Trials. 2018 Oct 5;19(1):540. doi: 10.1186/s13063-018-2867-1.
- Individual participant dataSharing planned: Undecided
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HIV, Substance Use Disorder
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Information provision, Weekly quizzes and Rewards for testing HIV-negative in people with HIV Infections and HIV, run by RAND at 1 site in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 5 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 10 Sep 2019. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
HIV knowledge (time frame: 12 months). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT03144336, which also lists 2 linked publications.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 10 Sep 2019.