Health BehaviorHealth Care UtilizationUnprotected SexSexually Transmitted Infections
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
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Review the details below, then apply to join this clinical trial.
At a Glance
Age
14 – 18
Sex
Female
Study type
Interventional
Purpose
Prevention
Participants needed
1,000 (estimated)
Sponsor
Child Trends · Other
Who this trial is looking for
This trial is looking for young people aged 14-18 assigned female or intersex at birth who want to improve their sexual health. Participants will use the SafeSpace app and complete a few surveys over one year.
Are You a Good Fit for This Trial?
You may be able to join if
I am assigned female or intersex at birth
I am between 14 and 18 years old
I live in the U.S.
I have daily access to an iPhone
You may not be able to join if
I am currently pregnant
I am trying to become pregnant
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer a few quick questions to see if you may meet the eligibility requirements.
The goal of this study is to evaluate the impact of SafeSpace Sexual Health App, an innovative sexual health promotion program focused on reducing sexual risk factors and promoting sexual and reproductive health and wellbeing among young people assigned female or intersex at birth, particularly Black and/or Latine youth, LGBTQ+ youth, youth in states with high teen birth rates and youth who live i…
The goal of this study is to evaluate the impact of SafeSpace Sexual Health App, an innovative sexual health promotion program focused on reducing sexual risk factors and promoting sexual and reproductive health and wellbeing among young people assigned female or intersex at birth, particularly Black and/or Latine youth, LGBTQ+ youth, youth in states with high teen birth rates and youth who live in rural communities. This study utilizes a two-arm randomized control trial design to measure impacts of receiving the SafeSpace Sexual Health program compared to receiving a similar-length control app program, SafeSpace General Health that focuses on general health.
The investigators will ask participants to:
* Keep the SafeSpace app downloaded to their device and visit the app regularly over the course of 10 weeks.
* Provide contact information.
* Receive and open app push notifications for 10 weeks (up to 3 per week).
* Complete 3 online surveys over a year: baseline, short-term follow-up (10 weeks after baseline), and long-term follow up (9 months after short-term follow-up).
* Receive occasional text messages from the study team.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Participants must be assigned female or intersex at birth
* Participants must be youth in the U.S. (14-18 years old)
* Participants must have daily access to an iPhone
Exclusion Criteria:
\- Participants must not be currently pregnant or currently trying to become pregnant
…
Inclusion Criteria:
* Participants must be assigned female or intersex at birth
* Participants must be youth in the U.S. (14-18 years old)
* Participants must have daily access to an iPhone
Exclusion Criteria:
\- Participants must not be currently pregnant or currently trying to become pregnant
Other Criteria:
\- The study's priority/preference population is for Black and/or Latine youth, LGBTQ+ youth, youth from geographic areas with high teen birth rates, and youth living in rural areas.
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