Pregnancy in AdolescenceWIUNCT06574321
Wrap It Up Rigorous Evaluation
A study testing Wrap It Up (WIU) in people with Pregnancy in Adolescence and Sexually Transmitted Diseases, run by ETR Associates at 1 site in United States.
Trial summary
Unintended pregnancy rates among teenagers are higher in rural counties than urban or suburban counties. Wrap It Up (WIU) is a sexual health education "booster" program for older high school students attending school in rural communities that was designed to help address this situation. Read more about this study
- Who is it for?
- Ages 16 to 19 yearsHealthy volunteers can take part
- Conditions the study is for
- Pregnancy in Adolescence, Sexually Transmitted Diseases
- What is being tested?
- Wrap It Up (WIU)
- Type of treatment
- Lifestyle or therapy programme
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 1,120 participants
- Where
- 1 siteUnited States
- Study dates
- 29 Oct 2024to Dec 2027
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
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 16 to 19 years
- All sexes
- Healthy volunteers accepted
- Child, Adult
Who may be able to join
- part of the class or group identified by their school
- 16 to 19 years old
- sufficient English language skills (as assessed by data collector) to take part in the TTHSR intervention
Who cannot join
- Under 16 years old
- 20 years old or over
- Insufficient English language skills (as assessed by data collector) to take part in the Wrap It Up intervention
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
About this study
Official title: Rigorous Evaluation of the Wrap It Up Intervention's Impact on Pregnancy Prevention Among Rural California Adolescents
Unintended pregnancy rates among teenagers are higher in rural counties than urban or suburban counties. Wrap It Up (WIU) is a sexual health education "booster" program for older high school students attending school in rural communities that was designed to help address this situation. Though there is preliminary evidence of the program's effectiveness, it has not yet been rigorously evaluated with a randomized controlled trial.
WIU is designed to equip 11th and 12th grade students with the knowledge and skills necessary to make informed sexual health decisions as they move from high school into adulthood, in order to prevent behavioral risk factors that contribute to unintended pregnancy and sexually transmitted infections. Most students this age will have received prior SHE. WIU is a 4-to-5-hour "booster" intervention, delivered during late high school, intended to enhance the effectiveness of previous SHE.
Read more
The study's primary research question is:
What is the impact at 6-months post baseline of WIU relative to a "business as usual" comparison condition on the proportion of youth who self-report they either did not have vaginal or anal sex, or used condoms or effective birth control when they had vaginal or anal sex, in the past 90 days?
The study's secondary research questions are:
- What is the impact at 6-months post baseline of WIU relative to a "business as usual" comparison condition on the proportion of youth who self-report improved self-efficacy for self-advocating with healthcare providers, peers, and partners about their sexual health?
- What is the impact at 6-months post-baseline of WIU relative to a "business as usual" comparison condition on the proportion of youth who self-report improved self-efficacy to find and access sexual health services?
- What is the impact at 12-months post-baseline of WIU relative to a "business as usual" comparison condition on the proportion of youth who self-report they either did not have vaginal or anal sex, or used condoms or effective birth control when they had vaginal or anal sex, in the past 90 days?
Read the detailed description
Background Unintended pregnancy rates among teenagers are higher in rural counties than urban or suburban counties. Wrap It Up (WIU) is a sexual health education (SHE) "booster" program for older high school students attending school in rural communities that was designed to help address this issue. Though there is preliminary evidence of the program's effectiveness, it has not yet been rigorously evaluated. With this study, ETR will rigorously evaluate the effectiveness of WIU with a randomized controlled trial.
WIU is designed to equip 11th and 12th grade students with the knowledge and skills necessary to make informed sexual health decisions as they move from high school into adulthood, in order to prevent behavioral risk factors that contribute to unintended pregnancy and sexually transmitted infections (STIs). This program was created by Health Connected, a non-profit organization with over 30 years' experience in creating, evaluating, training on, and disseminating comprehensive sexual health education to young people and their families throughout California. Health Connected is ETR's implementation partner in this study.
Most students this age will have received prior SHE. WIU is a 4-to-5-hour "booster" intervention, delivered during late high school, intended to enhance the effectiveness of previous SHE. The WIU program will be administered to groups in school settings, such as science classes or student advisory sessions. We will use trained sexuality education professionals supported by Health Connected to deliver the intervention.
Research Questions
The principal purpose of WIU is to decrease behaviors that contribute to unintended pregnancy and STIs in students and increase behaviors that support prevention and wellbeing. The study's primary research question is:
What is the impact at 6-months post baseline of WIU relative to a "business as usual" comparison condition on the proportion of youth who self-report they either did not have vaginal or anal sex, or used condoms or effective birth control when they had vaginal or anal sex, in the past 90 days?
The study's secondary research questions are:
- What is the impact at 6-months post baseline of WIU relative to a "business as usual" comparison condition on the proportion of youth who self-report improved self-efficacy for self-advocating with healthcare providers, peers, and partners about their sexual health?
- What is the impact at 6-months post-baseline of WIU relative to a "business as usual" comparison condition on the proportion of youth who self-report improved self-efficacy to find and access sexual health services?
- What is the impact at 12-months post-baseline of WIU relative to a "business as usual" comparison condition on the proportion of youth who self-report they either did not have vaginal or anal sex, or used condoms or effective birth control when they had vaginal or anal sex, in the past 90 days?
Study Design This evaluation is a cluster randomized controlled trial (RCT) using a "school by year" approach. The investigators' implementation partners, Health Connected, will engage 16 California schools serving rural students to participate in the study for 2 years. Eight of the participating schools will be randomly assigned to the "intervention-first" group and eight to the "comparison-first" group. Each school will serve as its own control. Thus, half of the 16 participating schools will receive WIU in their first year. The other half will be in the comparison-first group and will receive the WIU intervention in their second year. During the comparison group year, schools will administer their normal SHE. Each school has an equal chance of being in either the intervention-first or comparison-first group.
Recruitment and randomization will occur during year 1 for the first cohort of 8 schools and during project year 2 for the second cohort of 8 schools; implementation will occur over years 2 and 3 for the first cohort of schools and over years 3 and 4 for the second cohort.
Upon recruitment and before randomization, schools will commit to a specific context (e.g., grade level, class setting) for implementing WIU and agree to use that same context for enrollment, baseline data collection, and study implementation across both years of the study regardless of which condition they are randomized at initial enrollment.
Investigators intend to enroll up to 1,600 students (roughly 50 students per school per year). Between 2024 and 2027, the study will survey participating students three times: at baseline (before implementing the WIU program), 6 months post-baseline, and 12 months post-baseline. Students who provide complete outcome data on the baseline survey will be considered part of the study sample that underwent random assignment and used to calculate attrition.
Data Collection The study team plans to administer the baseline survey in-person at the school sites on tablets provided by ETR. Audio-assistance will be available for student participants, if needed. Data will be collected approximately 1-4 weeks prior to implementation, with comparable times for schools in the comparison group. The project team will offer up to three make-up sessions for the baseline survey. In the baseline survey, the project team will assess demographic characteristics (e.g., sex, race, educational status); potential moderators (e.g., age, race/ethnicity, relationship status); sexual behaviors (e.g., abstinence, having sex with/without condom or contraception use, number of partners); and potential mediators (contraception knowledge, contraception attitudes, pregnancy attitudes) that will be used to establish baseline equivalence of the analytic sample. The timing of the implementation may vary across schools; for example, at some participating schools, baseline data collection may occur in the fall, while for others, it may occur in the spring. However, within a specific school, the timing will be consistent across the two years of study implementation.
Survey data will be collected in the same manner for both treatment and control groups by local data collectors hired and trained by ETR. If youth are still enrolled in the same school, the 6-month and 12-month post-program surveys may be collected onsite in the same manner as the baseline survey, or collected online. For youth who are no longer enrolled in the same school, they will receive an email or text message with a unique link so the survey can be accessed and completed on a device of their choosing. ETR will use its field-tested, digital tracking mechanism to best support locating youth for follow-up surveys.
Analysis Plan Investigators plan to recruit 16 schools across two years and randomize each to an initial experimental condition. For the second year of a school's implementation, the school will serve in the experimental condition opposite from its initial assignment, so that each school serves as its own control; this results in a total of 32 school-by-year clusters. Each school must enroll grade 11 and grade 12 students to be eligible for participation.
The study intends to enroll up to 1,600 students in grades 11-12 across the 16 recruited schools. We anticipate an analytic sample size of 1,408 students (88% response rate) at the 6-month follow-up time point, and an analytic sample size of 1,280 students (80% response rate) at the 12-month follow-up time point. The project does not anticipate any cluster-level attrition during the study.
The study estimates a minimum detectable impact of 8.25 percentage points, relative to a 20 percent prevalence rate (or equivalently, a minimum detectable effect size of 0.17) for the primary outcome of sexual abstinence/use of contraception, measured at the 6-month follow-up. This is based on the following assumptions: alpha = 0.05, power (Beta) or 0.80, an expectation that the covariates will explain 20 percent of individual level variation and 50 percent of cluster level variation in the model, and an intraclass correlation (ICC) of 0.01. The calculation's assumed randomized sample size is 1,600 students, which corresponds to approximately 50 students per recruited school in a given year. This model assumes an 88% response rate at the 6-month follow-up and an 80% response rate at the 12-month follow-up for the secondary outcomes, and these are based on response rates in a recent evaluation of a high school program conducted in 20 schools. The evaluation's power calculation was conducted cognizant of data on California high schoolers' sexual activity, which indicates that 20% of high school students in the state are sexually active. The study settled on this minimum detectable impact based on a meta-analysis by Chin et al. (2012) of similar group-based, comprehensive sexual risk-reduction programs for adolescents, in which the average effect size corresponded to a Cohen's d of 0.19.
- Being tested
- Wrap It Up (WIU)
- Keywords
- Pregnancy in Adolescence, Prevention, Sexual Health, Sex Education
- Medical subject headings
- Sexually Transmitted Diseases
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Wrap It Up (WIU)Behavioural
WIU is designed to equip 11th and 12th grade students with the knowledge and skills necessary to make informed sexual health decisions as they move from high school into adulthood, in order to prevent behavioral risk factors that contribute to unintended pregnancy and sexually transmitted infections.
Most students this age will have received prior SHE. WIU is a 4-to-5-hour "booster" intervention, delivered in five 1-hour sessions during late high school, intended to enhance the effectiveness of previous SHE.
| Study group | Role | What they receive |
|---|---|---|
| WIU Intervention | Experimental | Intervention: Students in schools in this group will receive Wrap It Up, a 4-to-5-session SHE "booster" program Receives: Behavioral: Wrap It Up (WIU) |
| Comparison | No intervention | "Business-as-usual" control: Students in schools in this group will receive their school's normal classroom teaching |
What is being measured
The primary outcome is the main question the study is designed to answer.
No vaginal or anal sex, or use of condoms or effective birth control if having sex, in past 90 days
Vaginal sex: Single-item dichotomous measure assessing any consensual vaginal sex in the past 3 months. If yes, condom and birth control use measured with single-item categorical frequency of (a) condom use with consensual vaginal sex in past 3 months and (b) birth control use, other than condoms, with consensual vaginal sex in past 3 months. Categories: Every time, Almost every time, Most of the time, About half of the time, Less than half of the time, Just a few times, Never.
Anal sex: Single-item dichotomous measure assessing any consensual anal sex in the past 3 months. If yes, condom use measured with single-item categorical frequency of condom use with consensual anal sex in the past 3 months. Categories: Every time, Almost every time, Most of the time, About half of the time, Less than half of the time, Just a few times, Never.
Measured: 6 months post-baseline
Secondary outcomes (3)
Improved self-efficacy for self-advocating with healthcare providers, peers, and partners about sexual health
13 items (adapted from established measures) with categorical responses assessing how sure or unsure/ confident or unconfident respondents are about advocating for their own sexual health with healthcare providers and partners, and in situations of sexualized bullying with peers.
Measured: 6 months post-baseline
Improved self-efficacy to find and access sexual health services
4-item measure with categorical responses assessing how much respondents agree or disagree with statements about difficulty of accessing sexual health services and their confidence about doing so (adapted from measure reported in Manlove, J., Whitfield, B., Finocharo, J., \& Cook, E. (2021). Lessons learned from replicating a randomized control trial evaluation of an app-based sexual health program. International Journal of Environmental Research Public Health, 18(6), p. 3305.)
Measured: 6 months post-baseline
No vaginal or anal sex, or use of condoms or effective birth control if having sex, in past 90 days
Vaginal sex: Single-item dichotomous measure assessing any consensual vaginal sex in the past 3 months. If yes, condom and birth control use measured with single-item categorical frequency of (a) condom use with consensual vaginal sex in past 3 months and (b) birth control use, other than condoms, with consensual vaginal sex in past 3 months. Categories: Every time, Almost every time, Most of the time, About half of the time, Less than half of the time, Just a few times, Never.
Anal sex: Single-item dichotomous measure assessing any consensual anal sex in the past 3 months. If yes, condom use measured with single-item categorical frequency of condom use with consensual anal sex in the past 3 months. Categories: Every time, Almost every time, Most of the time, About half of the time, Less than half of the time, Just a few times, Never.
Measured: 12 months post-baseline
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted27 Aug 2024
- Study start29 Oct 2024
- Primary completionDec 2027 (estimated)
- Study completionDec 2027 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Pregnancy in AdolescenceStudies 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
- Model description
- This evaluation is a cluster RCT using a "school by year" approach. 16 California schools will participate for 2 years. 8 will be randomly assigned to the "intervention-first" group and 8 to the "comparison-first" group. Each school will serve as its own control and has an equal chance of being in either the intervention-first or the comparison-first group. During their comparison group year, schools will administer their normal sexual health education programming.
- Masking
- None (open label)
- Enrolment
- 1,120 participants (estimated)
Sponsor and investigators
- Lead sponsor
- ETR Associates
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- Pamela J Drake, PhD, Principal investigator, ETR Associates
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06574321
- Sponsor's protocol ID
- TP2AH000084
- Acronym
- WIU
- Status last verified
- Jan 2026
- First submitted
- 26 Aug 2024
- Last updated
- 23 Jan 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 23 Jan 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Rigorous Evaluation of the Wrap It Up Intervention's Impact on Pregnancy Prevention Among Rural California Adolescents
- ClinicalTrials.gov ID
- NCT06574321
- Acronym / sponsor ID
- WIU / TP2AH000084
- Keywords
- Pregnancy in Adolescence, Prevention, Sexual Health, Sex Education
- Study type
- Interventional
- Recruitment status
- Enrolling by invitation
- Enrolment
- 1,120 participants (estimated)
- Lead sponsor
- ETR AssociatesUniversity, hospital or other
- Study start
- 29 Oct 2024 (actual)
- Primary completion
- Dec 2027 (estimated)
- Study completion
- Dec 2027 (estimated)
- First posted
- 27 Aug 2024 (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.
Unintended pregnancy rates among teenagers are higher in rural counties than urban or suburban counties. Wrap It Up (WIU) is a sexual health education "booster" program for older high school students attending school in rural communities that was designed to help address this situation. Though there is preliminary evidence of the program's effectiveness, it has not yet been rigorously evaluated with a randomized controlled trial.
WIU is designed to equip 11th and 12th grade students with the knowledge and skills necessary to make informed sexual health decisions as they move from high school into adulthood, in order to prevent behavioral risk factors that contribute to unintended pregnancy and sexually transmitted infections. Most students this age will have received prior SHE. WIU is a 4-to-5-hour "booster" intervention, delivered during late high school, intended to enhance the effectiveness of previous SHE.
The study's primary research question is:
What is the impact at 6-months post baseline of WIU relative to a "business as usual" comparison condition on the proportion of youth who self-report they either did not have vaginal or anal sex, or used condoms or effective birth control when they had vaginal or anal sex, in the past 90 days?
The study's secondary research questions are:
- What is the impact at 6-months post baseline of WIU relative to a "business as usual" comparison condition on the proportion of youth who self-report improved self-efficacy for self-advocating with healthcare providers, peers, and partners about their sexual health?
- What is the impact at 6-months post-baseline of WIU relative to a "business as usual" comparison condition on the proportion of youth who self-report improved self-efficacy to find and access sexual health services?
- What is the impact at 12-months post-baseline of WIU relative to a "business as usual" comparison condition on the proportion of youth who self-report they either did not have vaginal or anal sex, or used condoms or effective birth control when they had vaginal or anal sex, in the past 90 days?
Detailed description
Background Unintended pregnancy rates among teenagers are higher in rural counties than urban or suburban counties. Wrap It Up (WIU) is a sexual health education (SHE) "booster" program for older high school students attending school in rural communities that was designed to help address this issue. Though there is preliminary evidence of the program's effectiveness, it has not yet been rigorously evaluated. With this study, ETR will rigorously evaluate the effectiveness of WIU with a randomized controlled trial.
WIU is designed to equip 11th and 12th grade students with the knowledge and skills necessary to make informed sexual health decisions as they move from high school into adulthood, in order to prevent behavioral risk factors that contribute to unintended pregnancy and sexually transmitted infections (STIs). This program was created by Health Connected, a non-profit organization with over 30 years' experience in creating, evaluating, training on, and disseminating comprehensive sexual health education to young people and their families throughout California. Health Connected is ETR's implementation partner in this study.
Most students this age will have received prior SHE. WIU is a 4-to-5-hour "booster" intervention, delivered during late high school, intended to enhance the effectiveness of previous SHE. The WIU program will be administered to groups in school settings, such as science classes or student advisory sessions. We will use trained sexuality education professionals supported by Health Connected to deliver the intervention.
Research Questions
The principal purpose of WIU is to decrease behaviors that contribute to unintended pregnancy and STIs in students and increase behaviors that support prevention and wellbeing. The study's primary research question is:
What is the impact at 6-months post baseline of WIU relative to a "business as usual" comparison condition on the proportion of youth who self-report they either did not have vaginal or anal sex, or used condoms or effective birth control when they had vaginal or anal sex, in the past 90 days?
The study's secondary research questions are:
- What is the impact at 6-months post baseline of WIU relative to a "business as usual" comparison condition on the proportion of youth who self-report improved self-efficacy for self-advocating with healthcare providers, peers, and partners about their sexual health?
- What is the impact at 6-months post-baseline of WIU relative to a "business as usual" comparison condition on the proportion of youth who self-report improved self-efficacy to find and access sexual health services?
- What is the impact at 12-months post-baseline of WIU relative to a "business as usual" comparison condition on the proportion of youth who self-report they either did not have vaginal or anal sex, or used condoms or effective birth control when they had vaginal or anal sex, in the past 90 days?
Study Design This evaluation is a cluster randomized controlled trial (RCT) using a "school by year" approach. The investigators' implementation partners, Health Connected, will engage 16 California schools serving rural students to participate in the study for 2 years. Eight of the participating schools will be randomly assigned to the "intervention-first" group and eight to the "comparison-first" group. Each school will serve as its own control. Thus, half of the 16 participating schools will receive WIU in their first year. The other half will be in the comparison-first group and will receive the WIU intervention in their second year. During the comparison group year, schools will administer their normal SHE. Each school has an equal chance of being in either the intervention-first or comparison-first group.
Recruitment and randomization will occur during year 1 for the first cohort of 8 schools and during project year 2 for the second cohort of 8 schools; implementation will occur over years 2 and 3 for the first cohort of schools and over years 3 and 4 for the second cohort.
Upon recruitment and before randomization, schools will commit to a specific context (e.g., grade level, class setting) for implementing WIU and agree to use that same context for enrollment, baseline data collection, and study implementation across both years of the study regardless of which condition they are randomized at initial enrollment.
Investigators intend to enroll up to 1,600 students (roughly 50 students per school per year). Between 2024 and 2027, the study will survey participating students three times: at baseline (before implementing the WIU program), 6 months post-baseline, and 12 months post-baseline. Students who provide complete outcome data on the baseline survey will be considered part of the study sample that underwent random assignment and used to calculate attrition.
Data Collection The study team plans to administer the baseline survey in-person at the school sites on tablets provided by ETR. Audio-assistance will be available for student participants, if needed. Data will be collected approximately 1-4 weeks prior to implementation, with comparable times for schools in the comparison group. The project team will offer up to three make-up sessions for the baseline survey. In the baseline survey, the project team will assess demographic characteristics (e.g., sex, race, educational status); potential moderators (e.g., age, race/ethnicity, relationship status); sexual behaviors (e.g., abstinence, having sex with/without condom or contraception use, number of partners); and potential mediators (contraception knowledge, contraception attitudes, pregnancy attitudes) that will be used to establish baseline equivalence of the analytic sample. The timing of the implementation may vary across schools; for example, at some participating schools, baseline data collection may occur in the fall, while for others, it may occur in the spring. However, within a specific school, the timing will be consistent across the two years of study implementation.
Survey data will be collected in the same manner for both treatment and control groups by local data collectors hired and trained by ETR. If youth are still enrolled in the same school, the 6-month and 12-month post-program surveys may be collected onsite in the same manner as the baseline survey, or collected online. For youth who are no longer enrolled in the same school, they will receive an email or text message with a unique link so the survey can be accessed and completed on a device of their choosing. ETR will use its field-tested, digital tracking mechanism to best support locating youth for follow-up surveys.
Analysis Plan Investigators plan to recruit 16 schools across two years and randomize each to an initial experimental condition. For the second year of a school's implementation, the school will serve in the experimental condition opposite from its initial assignment, so that each school serves as its own control; this results in a total of 32 school-by-year clusters. Each school must enroll grade 11 and grade 12 students to be eligible for participation.
The study intends to enroll up to 1,600 students in grades 11-12 across the 16 recruited schools. We anticipate an analytic sample size of 1,408 students (88% response rate) at the 6-month follow-up time point, and an analytic sample size of 1,280 students (80% response rate) at the 12-month follow-up time point. The project does not anticipate any cluster-level attrition during the study.
The study estimates a minimum detectable impact of 8.25 percentage points, relative to a 20 percent prevalence rate (or equivalently, a minimum detectable effect size of 0.17) for the primary outcome of sexual abstinence/use of contraception, measured at the 6-month follow-up. This is based on the following assumptions: alpha = 0.05, power (Beta) or 0.80, an expectation that the covariates will explain 20 percent of individual level variation and 50 percent of cluster level variation in the model, and an intraclass correlation (ICC) of 0.01. The calculation's assumed randomized sample size is 1,600 students, which corresponds to approximately 50 students per recruited school in a given year. This model assumes an 88% response rate at the 6-month follow-up and an 80% response rate at the 12-month follow-up for the secondary outcomes, and these are based on response rates in a recent evaluation of a high school program conducted in 20 schools. The evaluation's power calculation was conducted cognizant of data on California high schoolers' sexual activity, which indicates that 20% of high school students in the state are sexually active. The study settled on this minimum detectable impact based on a meta-analysis by Chin et al. (2012) of similar group-based, comprehensive sexual risk-reduction programs for adolescents, in which the average effect size corresponded to a Cohen's d of 0.19.
Study design
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
- Model description
- This evaluation is a cluster RCT using a "school by year" approach. 16 California schools will participate for 2 years. 8 will be randomly assigned to the "intervention-first" group and 8 to the "comparison-first" group. Each school will serve as its own control and has an equal chance of being in either the intervention-first or the comparison-first group. During their comparison group year, schools will administer their normal sexual health education programming.
| Arm | Type | Receives |
|---|---|---|
| WIU Intervention | Experimental | Behavioral: Wrap It Up (WIU)Intervention: Students in schools in this group will receive Wrap It Up, a 4-to-5-session SHE "booster" program |
| Comparison | No intervention | –"Business-as-usual" control: Students in schools in this group will receive their school's normal classroom teaching |
Who may qualify
- Ages
- 16 to 19 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Child, Adult
Key inclusion criteria (3 listed)
- part of the class or group identified by their school
- 16 to 19 years old
- sufficient English language skills (as assessed by data collector) to take part in the TTHSR intervention
Key exclusion criteria (3 listed)
- Under 16 years old
- 20 years old or over
- Insufficient English language skills (as assessed by data collector) to take part in the Wrap It Up intervention
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 |
|---|---|---|
| Wrap It Up (WIU)WIU is designed to equip 11th and 12th grade students with the knowledge and skills necessary to make informed sexual health decisions as they move from high school into adulthood, in order to prevent behavioral risk factors that contribute to unintended pregnancy and sexually transmitted infections. Most students this age will have received prior SHE. WIU is a 4-to-5-hour "booster" intervention, delivered in five 1-hour sessions during late high school, intended to enhance the effectiveness of previous SHE. | Behavioural | WIU Intervention |
Primary outcome
No vaginal or anal sex, or use of condoms or effective birth control if having sex, in past 90 days
Time frame: 6 months post-baseline
Vaginal sex: Single-item dichotomous measure assessing any consensual vaginal sex in the past 3 months. If yes, condom and birth control use measured with single-item categorical frequency of (a) condom use with consensual vaginal sex in past 3 months and (b) birth control use, other than condoms, with consensual vaginal sex in past 3 months. Categories: Every time, Almost every time, Most of the time, About half of the time, Less than half of the time, Just a few times, Never. Anal sex: Single-item dichotomous measure assessing any consensual anal sex in the past 3 months. If yes, condom use measured with single-item categorical frequency of condom use with consensual anal sex in the past 3 months. Categories: Every time, Almost every time, Most of the time, About half of the time, Less than half of the time, Just a few times, Never.
3 secondary outcomes
Improved self-efficacy for self-advocating with healthcare providers, peers, and partners about sexual health
Time frame: 6 months post-baseline
Improved self-efficacy to find and access sexual health services
Time frame: 6 months post-baseline
No vaginal or anal sex, or use of condoms or effective birth control if having sex, in past 90 days
Time frame: 12 months post-baseline
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 23 Jan 2026.
- Individual participant dataSharing planned: No
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Turner Syndrome, Post-menarcheal Adolescents
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.
Pamela J Drake, PhD principal investigator
ETR Associates
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Wrap It Up (WIU) in people with Pregnancy in Adolescence and Sexually Transmitted Diseases, run by ETR Associates 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 3 inclusion and 3 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: enrolling by invitation, as of the sponsor's last update on 23 Jan 2026. 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?
This study is still under way. Results are not available in the source record yet.
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?
No vaginal or anal sex, or use of condoms or effective birth control if having sex, in past 90 days (time frame: 6 months post-baseline). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
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 23 Jan 2026.