- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04108988
A Digital Intervention for HIV Prevention in Black Adolescent Girls
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
This study will develop and evaluate a multiplayer videogame aimed at Black adolescent girls with the intent of teaching the ability to negotiate around risk including advocating for partner HIV/STI testing, increasing their knowledge and awareness of HIV/STIs, and for reducing sexual risk-taking behaviors.
The intervention will be developed and delivered as a social, multiplayer videogame, a compelling context for Black adolescent girls who constantly interact and seek counsel from their peers. To this end, the Specific Aims, focusing on Black adolescent girls aged 14-18 years, are to:
- (Phase 1) Translate the culturally and socially-tailored card game One Night Stan to a multiplayer videogame called InvestiDate using game design and content experts and focus group input from 30 Black adolescent girls.
(Phase 2) Conduct a pilot randomized controlled trial comparing the multiplayer videogame InvestiDate (the new adaptation of the One Night Stan intervention) vs. an attention/control non-health-related multiplayer videogame with 80 participants collecting assessment data at baseline, one, and four months to:
- Determine the intervention's acceptability and feasibility by collecting quantitative and qualitative data on Black adolescent girls' satisfaction and gameplay experience of the intervention.
- Determine the preliminary impact of the intervention on knowledge (information), intentions/attitudes (motivation), social norms, and behavioral skills as related to: i) HIV/STI testing and partner testing and ii) condom use, and iii) sexual risk behavior reduction, such as alcohol and drug use.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Connecticut
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New Haven, Connecticut, United States, 06510
- Kimberly Hieftje
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
Both phases (includes focus groups- Phase 1)
- Black (race)
- Heterosexual
- Currently enrolled in high school
Pilot Test (Phase 2)
- Ability to participate in web-based videogame
- Willing to sit for at least 60 minutes (to play the game)
- No HIV testing in the last 12 months
- Ability to provide assent or parental/guardian consent
Exclusion Criteria:
- Failure to meet inclusion criteria
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Experimental: InvestiDate Intervention
One Night Stan will be adapted as a multiplayer videogame called InvestiDate based on the card game prototype with a focus on a slightly younger age group.
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Participants will be randomly assigned to play either InvestiDate (n=40), or the non-health related attention and time control condition multiplayer videogame (n=40).
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Placebo Comparator: Non-Health Related Game
Participants in the non-health related game group will play a multiplayer game unrelated to the content of InvestiDate.
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Participants will be randomly assigned to play either InvestiDate (n=40), or the non-health related attention and time control condition multiplayer videogame (n=40).
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Feasibility Assessed Using Change in Retention Rates
Time Frame: Baseline, 1 month and 4 months
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Feasibility of this intervention is assessed by the percent of total questionnaires returned out of all distributed at each time point to assess retention rates.
Rates >80% indicate high retention.
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Baseline, 1 month and 4 months
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Acceptability Assessed Via Self-reported Survey
Time Frame: 1 month
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Acceptability of the intervention condition is assessed via self-reported survey at the post gameplay time point using the game experience and satisfaction questionnaire, which is a 10-item scale with 4-point Likert-type responses ranging from 1 (strongly disagree) to 4 (strongly agree).
Total score range 10-40.
Data were collected from participants in the experimental group only.
Higher scores indicate stronger agreement with the statement.
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1 month
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Acceptability Assessed by Favorite Investidate Activities
Time Frame: Month 4
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Participants were asked to indicate (from a list) their favorite activity in the game.
The data presented here indicates the total number of participants in the experimental group that selected each activity as their favorite.
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Month 4
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Total Time Playing
Time Frame: Month 4
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The mean total time spent playing the videogame
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Month 4
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Change From Baseline at 4 Months: HIV/STI Testing- Self
Time Frame: Baseline, 1 month and 4 months
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HIV/STI Testing- self will be used to determine if individuals who play InvestiDate will report more HIV/STI testing and partner testing in comparison to the control condition.
Investigators will conduct a longitudinal analysis using a hierarchical linear mixed models approach to compare participants in the intervention group to participants in the control group on reported participant and partner HIV/STI testing from baseline across all follow-up assessments.
Data presented here shows the number of participants who said YES they had been tested out of the total number of participants in each group that responded to the question.
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Baseline, 1 month and 4 months
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Change From Baseline at 4 Months: HIV/STI Testing- Partner
Time Frame: Baseline, 1 month and 4 months
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HIV/STI Testing- partner will be used to test the hypothesis that individuals who play InvestiDate will report more HIV/STI testing and partner testing in comparison to the control condition.
The investigators will conduct a longitudinal analysis using a hierarchical linear mixed models approach to compare participants in the intervention group to participants in the control group on reported participant and partner HIV/STI testing from baseline across all follow-up assessments.
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Baseline, 1 month and 4 months
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Change in Use of Condoms
Time Frame: Baseline, 1 month and 4 months
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At each time point, participants responded to the item "Did you use a condom the last time you had sex?" Response options were "yes", "no", and "I have never had sex".
Data presented here shows the number of participants who answered YES out of the number of people in each group that responded to the question.
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Baseline, 1 month and 4 months
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Change in Self-Efficacy to Use Condoms (SECU) Using the Condom Use Self-Efficacy Scale (CUSES)
Time Frame: Baseline, 1 month, 4 months
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The CUSES is a 28 item self-report questionnaire which elicits responses using a five-point Likert scale format, ranging from 'strongly disagree' to 'strongly agree'.
10 of the 28 items were administered and scores were summed for each item for each participant.
Each of the responses is scored as follows: 'strongly disagree' = 0, 'disagree' = 1, 'undecided' = 2, 'agree' = 3 and 'strongly agree' = 4.
The possible range of scores is 0-40, with higher scores indicating greater self-efficacy.
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Baseline, 1 month, 4 months
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Change in SECU Using Sexual Risk Behavior Beliefs and Self-efficacy (SRBBS)
Time Frame: Baseline, 1 month, 4 months
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The SRBBS measure includes 3 items (e.g., "How sure ate you that you could use a condom correctly or explain to your partner how to use a condom correctly?")
measured on a scale from 1 (not sure at all) to 5 (extremely sure).
For each participant a mean of the 3 items was calculated.
Scores range from 1-5 with higher scores indicating higher levels of self-efficacy.
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Baseline, 1 month, 4 months
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Change in Self-efficacy in Refusing Sex (SER) Using the SER Subscale of the SRBBS
Time Frame: Baseline, 1 month and 4 months
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This subscale includes three items (e.g., "Imagine that you met someone at a party.
He or she wants to have sex with you.
Even though you are very attracted to each other, you're not ready to have sex.
How sure are you that you could keep from having sex") rated on a scale ranging from 1 (not sure at all) to 5 (extremely sure).
A mean score for the three items was calculated for each participant with score ranging from 1-5.
Higher scores indicating higher levels of self-efficacy for refusing sex.
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Baseline, 1 month and 4 months
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Change in Self-efficacy in Communication Using the Self-efficacy for Communication (SECM) Subscale of the SRBBS
Time Frame: Baseline, 1 month and 4 months
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Self-efficacy for communication was assessed using the SECM subscale of the SRBBS.
This subscale includes three items (e.g., "Imagine that you and your partner have been having sex but have not used condoms.
You really want to start using condoms.
How sure are you that you could tell that person that you want to use condoms") rated on a scale ranging from 1 (not sure at all) to 5 (extremely sure).
A mean score for the three items was calculated for each participant with score ranging from 1-5.
Higher scores indicating higher levels of communication.
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Baseline, 1 month and 4 months
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Change in Self-efficacy for PrEP
Time Frame: Baseline, 1 month and 4 months
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Self-Efficacy for using PrEP was assessed with a 4 item survey.
Each item was measured on a scale ranging from 1 (strongly disagree) to 5 (strongly agree).
A mean score for the three items was calculated for each participant with score ranging from 1-5.
Higher scores indicating higher levels of self-efficacy.
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Baseline, 1 month and 4 months
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Change in Attitudes About Condom Use (ACU) Assessed Using the ACU Subscale of the SRBBS
Time Frame: Baseline, 1 month and 4 months
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Attitudes about condom use were assessed using the ACU subscale of the SRBBS.
This subscale includes three items scored from -2 (strongly disagree) to +2 (strongly agree).
A mean score was calculated for each participant with negative mean scores indicating negative (unhealthy) attitudes about condom use and positive scores indicating positive (healthy) attitudes about condom use.
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Baseline, 1 month and 4 months
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Change in Attitudes About Sexual Intercourse (ASI) Were Assessed Using the ASI Subscale of the SRBBS
Time Frame: Baseline, 1 month and 4 months
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Attitudes about sexual intercourse were assessed using the ASI subscale of the SRBBS.
This subscale includes three items scored from -2 (strongly disagree) to +2 (strongly agree).
A mean score was calculated for each participant with negative mean scores indicating negative (unhealthy) attitudes about condom use and positive scores indicating positive (healthy) attitudes about sexual intercourse.
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Baseline, 1 month and 4 months
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Change in Intentions to Find a Clinic to Speak to a Doctor About PrEP
Time Frame: Baseline, 1 months and 4 months
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Intentions were measured with one item ("I intend to find a clinic in my community where I can speak to a doctor or health care provider about PrEP").
A mean score for the three items was calculated for each participant with score ranging from 1-5.
Higher scores indicating stronger intentions.
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Baseline, 1 months and 4 months
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Change in Sexually Transmitted Infections (STI)/HIV Knowledge
Time Frame: Baseline, 1 months and 4 months
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STI/HIV knowledge was assessed using 12 questions for which participants could answer "true", "false", or "not sure".
The answers were recoded as correct or incorrect, with "not sure" being coded as incorrect, and a sum was calculated for each participant.
Scores range from 0 - 12 with higher scores indicating more STI-HIV knowledge.
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Baseline, 1 months and 4 months
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Change in Norms About Condom Use (NCU) Assessed Using the NCU Subscale of the SRBBS
Time Frame: Baseline, 1 months and 4 months
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Norms about condom use were assessed using the NCU subscale of the SRBBS.
This subscale includes three items scored from -2 (strongly disagree) to +2 (strongly agree).
A mean score was calculated for each participant with negative mean scores indicating negative (unhealthy) perceived about condom use and positive scores indicating positive (healthy) perceived norms about sexual intercourse.
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Baseline, 1 months and 4 months
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Change in Norms About Intercourse (NSI) Assessed Using the NSI Subscale of the SRBBS
Time Frame: Baseline, 1 months and 4 months
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Norms about sexual intercourse were assessed using the NSI subscale of the SRBBS.
This subscale includes three items scored from -2 (strongly disagree) to +2 (strongly agree).
A mean score was calculated for each participant with negative mean scores indicating negative (unhealthy) perceived about condom use and positive scores indicating positive (healthy) perceived norms about sexual intercourse.
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Baseline, 1 months and 4 months
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Change in Perceived Norms About PrEP
Time Frame: Baseline, 1 months and 4 months
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Perceived norms about the use of PrEP were assessed using a 2 item survey.
Both items were rated from 1 (not at all) to 4 (a lot).
A mean of the two items was calculated for each participant with score ranging from 1-4.
Higher scores indicate more positive perceived norms about the use of PrEP.
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Baseline, 1 months and 4 months
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Change in Barriers to Condom Use (BCU) Assessed Using the BCU Subscale of the SRBBS
Time Frame: Baseline, 1 months and 4 months
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The BCU subscale includes six items assessed on a scale ranging from 1 (strongly disagree) to 5 (strongly agree).
A mean score was calculated for each participant with score ranging from 1-5.
Higher scores indicating more perceived barriers to condom use.
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Baseline, 1 months and 4 months
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Change in Behavior of Purchasing Condoms
Time Frame: Baseline, 1 month and 4 months
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Participants reported on whether they had purchased condoms ever (baseline) or since they first played the videogame over zoom as part of this research study (1 month, 4 months).
The response options were "yes" or "no".
Data presented here shows the number of participants who answered YES out of the number of people in each group that responded to the question.
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Baseline, 1 month and 4 months
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Change in Behavior of Having Looked up a Place to Get HIV or STI Testing
Time Frame: Baseline, 1 month and 4 months
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Participants reported on whether they had looked up a place to get HIV or STI testing ever (baseline) or since they first played the videogame over zoom as part of this research study (1 month, 4 months).
The response options were "yes" or "no".
Data presented here shows the number of participants who answered YES out of the number of people in each group that responded to the question.
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Baseline, 1 month and 4 months
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Change in Behavior of Having Talked With Partner About Getting Tested for HIV or STI
Time Frame: Baseline, 1 month and 4 months
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Participants reported on whether they had talked with a partner about getting tested for HIV or STIs ever (baseline) or since they first played the videogame over zoom as part of this research study (1 month, 4 months).
The response options were "yes" or "no".
Data presented here shows the number of participants who answered YES out of the number of people in each group that responded to the question.
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Baseline, 1 month and 4 months
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Change in Birth Control Use
Time Frame: Baseline, 1 month and 4 months
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Participants were asked to indicate if they used birth control last time they had sex.
The response options were "yes", "no", and "I have never had sex".
Data presented here shows the number of participants who answered YES out of the number of people in each group that responded to the question.
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Baseline, 1 month and 4 months
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Change in Behavior Regarding Refusal to Have Sex
Time Frame: 1 month and 4 months
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At 1 month and 4 months, participants were asked if they had refused to have sex with a partner because he would not use a condom in the time since they first played the videogame over zoom as part of this research study.
The response options were "yes" or "no".
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1 month and 4 months
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Number of Participants Refusal to Have Sex
Time Frame: Baseline
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At baseline participants were asked to indicate if they had refused to have sex with a partner because he would not use a condom ever.
Response options were "always", "most of the time", "about half the time", "sometimes", and "never".
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Baseline
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Number of Participants That Asked Partner About Previous Condom Use
Time Frame: Baseline
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At baseline participants were asked how often they ask their sexual partners whether or not they have used a condom in previous sexual encounters?
Response options were "always", "most of the time", "about half the time", "sometimes", and "never".
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Baseline
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Number of Times Participants Asked Partner About Previous Condom Use
Time Frame: 1 month and 4 months
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At 1 month and 4 months, participants were asked how many times they discussed condom use with a sexual partner since first playing the videogame on zoom as part of this research study.
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1 month and 4 months
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Number of Times Participants Talked to Family or Adults About HIV
Time Frame: baseline, 1 month and 4 months
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Participants were asked how many times they had talked with their family or other adults about HIV ever (baseline) or since they played the videogame on zoom as part of this research study (1 month, 4 months).
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baseline, 1 month and 4 months
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Number of Times Participants Engaged in Sexual Intercourse
Time Frame: baseline, 1 month and 4 months
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Participants were asked how many times they had engaged in sexual intercourse ever (baseline, post-intervention) or since playing the videogame on zoom as part of this research study (1 month, 4 months).
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baseline, 1 month and 4 months
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Number of Times Participants Engaged in Anal Sex
Time Frame: baseline, 1 month and 4 months
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Participants were asked how many times they had engaged in anal sex ever (baseline) or since playing the videogame on zoom as part of this research study (1 month, 4 months).
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baseline, 1 month and 4 months
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Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Kimberly Hieftje, PhD, Yale University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 2000026487
- 1R21HD098031-01 (U.S. NIH Grant/Contract)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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