Pregnancy RelatedNCT04079608
Rigorous Evaluation of High School FLASH
A study testing FLASH curriculum and Sexual Health Education for Adolescents in people with Pregnancy Related and Sexual Behavior, run by ETR Associates at 1 site in United States.
Trial summary
High School FLASH is a 15-session comprehensive sexual health curriculum designed for classroom settings in grades 9 to 12. The basis of High School FLASH is a public health approach to behavior change. Read more about this study
- Who is it for?
- Ages 14 to 18 yearsHealthy volunteers can take part
- Conditions the study is for
- Pregnancy Related, Sexual Behavior, STD
- What is being tested?
- FLASH curriculum and Sexual Health Education for Adolescents
- Type of treatment
- Lifestyle or therapy programme
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 1,597 participants
- Where
- 1 siteUnited States
- Study dates
- 5 Oct 2016to 30 Jun 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 14 to 18 years
- All sexes
- Healthy volunteers accepted
- Child, Adult
Who may be able to join
- District level eligibility: Districts must have been from regions with teen birth rates at or above the national average at the time of study recruitment. They also much have agreed with randomization of mainstream schools to either High School FLASH or the five-session knowledge-based comparison condition. We worked with 7 different districts in two different regions of the U.S. - the Midwest (2 districts) and the South (5 districts).
- School level eligibility: Schools were eligible to participate if they: (1) agreed with inviting all students in targeted grade level in the fall semester required class to take part in the study (9th or 10th grades depending on health education course placement); (2) had a policy environment that enabled implementation of all FLASH components if randomized to intervention condition; (3) were in a district not currently mandating comprehensive sexuality education or using an evidence-based sexual health curriculum in school or for after-school programs; and (4) have schools large enough to ideally contribute 40 or more students to the study.
- Student level eligibility: Student enrollment into the study must have included (1) being in targeted classes during the enrollment window (fall semester 2016 in the Midwest and fall semester 2017 in the South), (2) providing positive parent consent to take part in study survey; and (3) providing assent to take part in the survey.
Who cannot join
- Anyone not meeting inclusion criteria
Trial locations and contacts
1 site in 1 country.
About this study
High School FLASH is a 15-session comprehensive sexual health curriculum designed for classroom settings in grades 9 to 12. The basis of High School FLASH is a public health approach to behavior change. The primary strategy used in the FLASH curriculum for preventing teen pregnancy, sexually transmitted diseases (STDs), and sexual violence is to address student behaviors and attitudes. To this end, FLASH uses a harm reduction and behavior change framework, implements best practices as outlined in the research on effective programs, addresses risk and protective factors for program goals, and rests on the theory of planned behavior. The instructional approach of High School FLASH employs key concepts in every lesson, which enables teachers to hone in on the risk and protective factors outlined in the curriculum logic model. The curriculum covers the following topics: reproductive system, pregnancy, sexual orientation and gender identity, healthy relationships, coercion and consent, online safety, abstinence, birth control, preventing human immunodeficiency virus (HIV) and other STDs, condoms, STD testing, communicating and decision making, and improving school health. The curriculum aligns with national health education standards.
Read the detailed description
High School FLASH is a 15-session comprehensive sexual health curriculum designed for classroom settings in grades 9 to 12. The basis of High School FLASH is a public health approach to behavior change. The primary strategy used in the FLASH curriculum for preventing teen pregnancy, sexually transmitted diseases (STDs), and sexual violence is to address student behaviors and attitudes. To this end, FLASH uses a harm reduction and behavior change framework, implements best practices as outlined in the research on effective programs, addresses risk and protective factors for program goals, and rests on the theory of planned behavior. The instructional approach of High School FLASH employs key concepts in every lesson, which enables teachers to hone in on the risk and protective factors outlined in the curriculum logic model. The curriculum covers the following topics: reproductive system, pregnancy, sexual orientation and gender identity, healthy relationships, coercion and consent, online safety, abstinence, birth control, preventing human immunodeficiency virus (HIV) and other STDs, condoms, STD testing, communicating and decision making, and improving school health. The curriculum aligns with national health education standards. FLASH is ideally taught 2-5 times per week for 15 sessions lasting 50 minutes, or 10 sessions lasting 70-80 minutes, covering the same content. The curriculum is designed to be flexible to ensure sustainability in a variety of school environments.
The counterfactual condition is called Sexual Health Education for Adolescents, which is a five-session knowledge-based sexual health curriculum designed for classroom settings. The lessons cover the reproductive system, pregnancy, birth control, abstinence, HIV and other STDs, and healthy relationships. The goal of the curriculum is to increase student knowledge in all content areas. The primary strategy employed by Sexual Health Education for Adolescents is to address the cognitive learning domain. The curriculum aligns to national health education standards and is intended to be implemented by classroom teachers. The lessons can be delivered according to the schedule that works best for schools (e.g., twice a week, once a week, every days) within a school semester.
Students were recruited from 9th (South) or 10th (Midwest) grade health classes. The research team met with district and school administrators and health teachers to explain the study, data collection processes, and to answer questions. The FLASH study enrolled students from required health classes from 20 schools in the South and the Midwest. In the Midwest, we worked with two districts; one of the districts contributed 9 of the 10 high schools and the other district contributed one high school to the evaluation study. In the South, we have partnered with 10 schools in 5 counties, representing 5 different districts. One of these districts contributed 6 schools to the evaluation study and the remaining 4 districts each contributed 1 high school to the study.
Randomization was staggered and rolled-out by region to ensure that implementation started at the same time for all schools but only started in one region at a time. School enrollment was used as a stratification variable, so that schools assignments to the intervention and control arm were balanced within stratum. Randomization was performed within each region at the school level and was stratified into two categories by school size. For the Midwest region, small was defined as <500 enrollment and large was =>1000. For the Southern region, small was defined as <700 enrollment and large was =>700.
Active parental consent and student assent were obtained prior to any data collection. The steps in the consent process are discussed below:
- Two weeks or more prior to the surveys (as determined by the participating schools), evaluation staff went to each participating health class and provided an overview of the study and distributed parent consent forms to all students in the class, requesting that they take them home to their parents for review and return the signed forms to their classroom teacher with parents' decisions regarding participation marked on the form. In the Southern schools, students received a gift card worth $10 for returning parent consent forms. The Midwestern schools' administration would not allow for the distribution of any type of incentives; thus, these schools received a class reward for taking part in the parent consent process and reaching a threshold (e.g., 75% or more of students return parent consent regardless of whether parents say "yes" or "no"). All consent forms were translated into languages requested by each district.
- Evaluation staff returned multiple times (e.g., 2-3) during the collection period as agreed upon with the classroom teacher to check on the parent consent return rates and did brief reminders to students.
- Between evaluation staff visits to the classrooms, teachers were asked to remind students to return parent consent forms daily over the collection period and provided additional forms to students who needed them.
- After two weeks, evaluation staff worked with the schools to make calls to parents using a scripted protocol to read the consent form over the phone and secure parents' decisions or send them the form for them to return it by mail with their decision. In nine schools within one district in the Midwest region, we trained their nursing office staff (which included Health Educational Assistants and Licensed Practical Nurses) to make verbal consent calls home to parents at the request of district administration. These staff members are already responsible for communicating with parents about health-related matters and given that this was a health-related research study, the administration felt that these calls would be better received by their staff, rather than unfamiliar data collectors.
The primary source of data for the outcome analyses is the student self-report survey. The survey was administered three times over the course of the study. In the Midwest region this occurred: Fall 2016 (baseline), Spring 2017 (3-month follow-up), and Fall-Winter 2017-2018 (12-month follow-up). In the Southern region, data collection took place: Fall 2017 (baseline), Spring 2018 (3-month follow-up) and Fall-Winter 2018-2019 (12-month follow-up). Data were collected by trained data collectors in schools using handheld tablets. For students who left school after baseline but before follow-up surveys could be administered, we worked to survey these students at their new schools, online, or by mail.
- Conditions
- Pregnancy Related, Sexual Behavior, STD
- Being tested
- FLASH curriculum, Sexual Health Education for Adolescents
- Keywords
- Pregnancy, Adolescents, STD, Decision making, Harm reduction, Prevention education
- Medical subject headings
- Sexual Behavior, Harm Reduction
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
FLASH curriculumBehavioural
High School FLASH is a 15-session comprehensive sexual health curriculum designed for classroom settings in grades 9 to 12. The basis of High School FLASH is a public health approach to behavior change. The primary strategy used in the FLASH curriculum for preventing teen pregnancy, sexually transmitted diseases (STDs), and sexual violence is to address student behaviors and attitudes. To this end, FLASH uses a harm reduction and behavior change framework, implements best practices as outlined in the research on effective programs, addresses risk and protective factors for program goals, and rests on the theory of planned behavior. The instructional approach of High School FLASH employs key concepts in every lesson, which enables teachers to hone in on the risk and protective factors outlined in the curriculum logic model.
Sexual Health Education for AdolescentsBehavioural
Sexual Health Education for Adolescents is a five-session knowledge-based sexual health curriculum designed for classroom settings. The lessons cover the reproductive system, pregnancy, birth control, abstinence, human immunodeficiency virus (HIV) and other sexually transmitted diseases (STDs), and healthy relationships. The goal of the curriculum is to increase student knowledge in all content areas. The primary strategy employed by Sexual Health Education for Adolescents is to address the cognitive learning domain. The curriculum aligns to national health education standards and is intended to be implemented by classroom teachers. The lessons can be delivered according to the schedule that works best for schools (e.g., twice a week, once a week, every days) within a school semester.
| Study group | Role | What they receive |
|---|---|---|
| FLASH curriculum | Experimental | Students who will receive the FLASH high school curriculum. Receives: Behavioral: FLASH curriculum |
| Sexual Health Education for Adolescents | Active comparator | Students will receive a five-session knowledge-based sexual health curriculum designed for classroom settings. Receives: Behavioral: Sexual Health Education for Adolescents |
What is being measured
The primary outcome is the main question the study is designed to answer.
Self-reported rates of vaginal sex
Measured with a single item required and provided by the funder: "In the past 3 months, have you had vaginal intercourse, even once?" Yes/No
Measured: 3 months post-intervention
Self-reported rates of vaginal sex
Measured with a single item required and provided by the funder: "In the past 3 months, have you had vaginal intercourse, even once?" Yes/No
Measured: 12 months post-intervention
Self-reported rates of vaginal sex without a condom or other birth control
Combined the following two questions required and provided by the funder: "In the past 3 months, have you had vaginal intercourse without you or your partner using a condom?" and "In the past 3 months, how many times have you had vaginal intercourse without you or your partner using any of these methods of birth control: birth control pills, the shot, the patch, the ring, intrauterine device (IUD), or Implant" New outcome was coded 'yes' if either question was endorsed and 'no' if both questions were responded to as 'no'
Measured: 3 months post-intervention
Self-reported rates of vaginal sex without a condom or other birth control
Combined the following two questions required and provided by the funder: "In the past 3 months, have you had vaginal intercourse without you or your partner using a condom?" and "In the past 3 months, how many times have you had vaginal intercourse without you or your partner using any of these methods of birth control: birth control pills, the shot, the patch, the ring, intrauterine device (IUD), or Implant" New outcome was coded 'yes' if either question was endorsed and 'no' if both questions were responded to as 'no'
Measured: 12 months post-intervention
Secondary outcomes (6)
Self-reported initiation of vaginal sex
Measured with a single item required and provided by the funder: "Have you ever had vaginal sex?" Coding is 0 = 'no', 1 = 'yes'. This will only be analyzed on subjects reporting no to this same question at baseline.
Measured: 3 months post-intervention
Self-reported initiation of vaginal sex
Measured with a single item required and provided by the funder: "Have you ever had vaginal sex?" Coding is 0 = 'no', 1 = 'yes'. This will only be analyzed on subjects reporting no to this same question at baseline.
Measured: 12 months post-intervention
Self-reported knowledge of sexually transmitted disease (STD) testing
There are three knowledge measures developed specifically for this study around STD testing. "Have you heard of a clinic or doctor in your community where teens can get sexual health information and tests?" Coded 'yes', 'no', and 'not sure'. "If you needed to be tested, how comfortable would you be going to a clinic to be tested for STDs and HIV?" and "Imagine you or a friend wanted to get an STD test. How sure are you that you could go or help a friend to go to a clinic and get it?" both coded using a 4 point scale ranging from 'Very sure' or 'Very comfortable' to 'Not sure at all' or 'Not at all comfortable'.
Measured: 3 months post-intervention
Self-reported knowledge of sexually transmitted disease (STD) testing
There are three knowledge measures developed specifically for this study around STD testing. "Have you heard of a clinic or doctor in your community where teens can get sexual health information and tests?" Coded 'yes', 'no', and 'not sure'. "If you needed to be tested, how comfortable would you be going to a clinic to be tested for STDs and HIV?" and "Imagine you or a friend wanted to get an STD test. How sure are you that you could go or help a friend to go to a clinic and get it?" both coded using a 4 point scale ranging from 'Very sure' or 'Very comfortable' to 'Not sure at all' or 'Not at all comfortable'.
Measured: 12 months post-intervention
Self-reported comfort with family communication regarding sexual health
This is measured using the following two questions developed specifically for this study: "How comfortable are you talking about relationships, sexual health, or sex with your mother or female guardian?" "How comfortable are you talking about relationships, sexual health, or sex with your father or male guardian?" Coded 1 = 'comfortable', 2 = 'not comfortable'
Measured: 3 months post-intervention
Self-reported comfort with family communication regarding sexual health
This is measured using the following two questions developed specifically for this study: "How comfortable are you talking about relationships, sexual health, or sex with your mother or female guardian?" "How comfortable are you talking about relationships, sexual health, or sex with your father or male guardian?" Coded 1 = 'comfortable', 2 = 'not comfortable'
Measured: 12 months post-intervention
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted6 Sep 2019
- Study start5 Oct 2016
- Primary completion30 Jan 2019
- Study completion30 Jun 2019
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Pregnancy RelatedStudies 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
- None (open label)
- Enrolment
- 1,597 participants (actual)
Sponsor and investigators
- Lead sponsor
- ETR Associates
- Sponsor type
- University, hospital or other
- Collaborators
- Public Health Seattle King County
- Responsible party
- Sponsor
- Investigators
- Karin Coyle, PhD, Principal investigator, ETR
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT04079608
- Sponsor's protocol ID
- FLASH study
- Status last verified
- Sep 2019
- First submitted
- 3 Sep 2019
- Last updated
- 11 Sep 2019
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 11 Sep 2019. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Rigorous Evaluation of High School FLASH
- ClinicalTrials.gov ID
- NCT04079608
- Acronym / sponsor ID
- FLASH study
- Conditions
- Pregnancy Related, Sexual Behavior, STD
- Keywords
- Pregnancy, Adolescents, STD, Decision making, Harm reduction, Prevention education
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 1,597 participants (actual)
- Lead sponsor
- ETR AssociatesUniversity, hospital or other
- Collaborators
- Public Health Seattle King County
- Study start
- 5 Oct 2016 (actual)
- Primary completion
- 30 Jan 2019 (actual)
- Study completion
- 30 Jun 2019 (actual)
- First posted
- 6 Sep 2019 (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.
High School FLASH is a 15-session comprehensive sexual health curriculum designed for classroom settings in grades 9 to 12. The basis of High School FLASH is a public health approach to behavior change. The primary strategy used in the FLASH curriculum for preventing teen pregnancy, sexually transmitted diseases (STDs), and sexual violence is to address student behaviors and attitudes. To this end, FLASH uses a harm reduction and behavior change framework, implements best practices as outlined in the research on effective programs, addresses risk and protective factors for program goals, and rests on the theory of planned behavior. The instructional approach of High School FLASH employs key concepts in every lesson, which enables teachers to hone in on the risk and protective factors outlined in the curriculum logic model. The curriculum covers the following topics: reproductive system, pregnancy, sexual orientation and gender identity, healthy relationships, coercion and consent, online safety, abstinence, birth control, preventing human immunodeficiency virus (HIV) and other STDs, condoms, STD testing, communicating and decision making, and improving school health. The curriculum aligns with national health education standards.
Detailed description
High School FLASH is a 15-session comprehensive sexual health curriculum designed for classroom settings in grades 9 to 12. The basis of High School FLASH is a public health approach to behavior change. The primary strategy used in the FLASH curriculum for preventing teen pregnancy, sexually transmitted diseases (STDs), and sexual violence is to address student behaviors and attitudes. To this end, FLASH uses a harm reduction and behavior change framework, implements best practices as outlined in the research on effective programs, addresses risk and protective factors for program goals, and rests on the theory of planned behavior. The instructional approach of High School FLASH employs key concepts in every lesson, which enables teachers to hone in on the risk and protective factors outlined in the curriculum logic model. The curriculum covers the following topics: reproductive system, pregnancy, sexual orientation and gender identity, healthy relationships, coercion and consent, online safety, abstinence, birth control, preventing human immunodeficiency virus (HIV) and other STDs, condoms, STD testing, communicating and decision making, and improving school health. The curriculum aligns with national health education standards. FLASH is ideally taught 2-5 times per week for 15 sessions lasting 50 minutes, or 10 sessions lasting 70-80 minutes, covering the same content. The curriculum is designed to be flexible to ensure sustainability in a variety of school environments.
The counterfactual condition is called Sexual Health Education for Adolescents, which is a five-session knowledge-based sexual health curriculum designed for classroom settings. The lessons cover the reproductive system, pregnancy, birth control, abstinence, HIV and other STDs, and healthy relationships. The goal of the curriculum is to increase student knowledge in all content areas. The primary strategy employed by Sexual Health Education for Adolescents is to address the cognitive learning domain. The curriculum aligns to national health education standards and is intended to be implemented by classroom teachers. The lessons can be delivered according to the schedule that works best for schools (e.g., twice a week, once a week, every days) within a school semester.
Students were recruited from 9th (South) or 10th (Midwest) grade health classes. The research team met with district and school administrators and health teachers to explain the study, data collection processes, and to answer questions. The FLASH study enrolled students from required health classes from 20 schools in the South and the Midwest. In the Midwest, we worked with two districts; one of the districts contributed 9 of the 10 high schools and the other district contributed one high school to the evaluation study. In the South, we have partnered with 10 schools in 5 counties, representing 5 different districts. One of these districts contributed 6 schools to the evaluation study and the remaining 4 districts each contributed 1 high school to the study.
Randomization was staggered and rolled-out by region to ensure that implementation started at the same time for all schools but only started in one region at a time. School enrollment was used as a stratification variable, so that schools assignments to the intervention and control arm were balanced within stratum. Randomization was performed within each region at the school level and was stratified into two categories by school size. For the Midwest region, small was defined as <500 enrollment and large was =>1000. For the Southern region, small was defined as <700 enrollment and large was =>700.
Active parental consent and student assent were obtained prior to any data collection. The steps in the consent process are discussed below:
- Two weeks or more prior to the surveys (as determined by the participating schools), evaluation staff went to each participating health class and provided an overview of the study and distributed parent consent forms to all students in the class, requesting that they take them home to their parents for review and return the signed forms to their classroom teacher with parents' decisions regarding participation marked on the form. In the Southern schools, students received a gift card worth $10 for returning parent consent forms. The Midwestern schools' administration would not allow for the distribution of any type of incentives; thus, these schools received a class reward for taking part in the parent consent process and reaching a threshold (e.g., 75% or more of students return parent consent regardless of whether parents say "yes" or "no"). All consent forms were translated into languages requested by each district.
- Evaluation staff returned multiple times (e.g., 2-3) during the collection period as agreed upon with the classroom teacher to check on the parent consent return rates and did brief reminders to students.
- Between evaluation staff visits to the classrooms, teachers were asked to remind students to return parent consent forms daily over the collection period and provided additional forms to students who needed them.
- After two weeks, evaluation staff worked with the schools to make calls to parents using a scripted protocol to read the consent form over the phone and secure parents' decisions or send them the form for them to return it by mail with their decision. In nine schools within one district in the Midwest region, we trained their nursing office staff (which included Health Educational Assistants and Licensed Practical Nurses) to make verbal consent calls home to parents at the request of district administration. These staff members are already responsible for communicating with parents about health-related matters and given that this was a health-related research study, the administration felt that these calls would be better received by their staff, rather than unfamiliar data collectors.
The primary source of data for the outcome analyses is the student self-report survey. The survey was administered three times over the course of the study. In the Midwest region this occurred: Fall 2016 (baseline), Spring 2017 (3-month follow-up), and Fall-Winter 2017-2018 (12-month follow-up). In the Southern region, data collection took place: Fall 2017 (baseline), Spring 2018 (3-month follow-up) and Fall-Winter 2018-2019 (12-month follow-up). Data were collected by trained data collectors in schools using handheld tablets. For students who left school after baseline but before follow-up surveys could be administered, we worked to survey these students at their new schools, online, or by mail.
Study design
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| FLASH curriculum | Experimental | Behavioral: FLASH curriculumStudents who will receive the FLASH high school curriculum. |
| Sexual Health Education for Adolescents | Active comparator | Behavioral: Sexual Health Education for AdolescentsStudents will receive a five-session knowledge-based sexual health curriculum designed for classroom settings. |
Who may qualify
- Ages
- 14 to 18 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Child, Adult
Key inclusion criteria (3 listed)
- District level eligibility: Districts must have been from regions with teen birth rates at or above the national average at the time of study recruitment. They also much have agreed with randomization of mainstream schools to either High School FLASH or the five-session knowledge-based comparison condition. We worked with 7 different districts in two different regions of the U.S. - the Midwest (2 districts) and the South (5 districts).
- School level eligibility: Schools were eligible to participate if they: (1) agreed with inviting all students in targeted grade level in the fall semester required class to take part in the study (9th or 10th grades depending on health education course placement); (2) had a policy environment that enabled implementation of all FLASH components if randomized to intervention condition; (3) were in a district not currently mandating comprehensive sexuality education or using an evidence-based sexual health curriculum in school or for after-school programs; and (4) have schools large enough to ideally contribute 40 or more students to the study.
- Student level eligibility: Student enrollment into the study must have included (1) being in targeted classes during the enrollment window (fall semester 2016 in the Midwest and fall semester 2017 in the South), (2) providing positive parent consent to take part in study survey; and (3) providing assent to take part in the survey.
Key exclusion criteria (1 listed)
- Anyone not meeting inclusion criteria
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 |
|---|---|---|
| FLASH curriculumHigh School FLASH is a 15-session comprehensive sexual health curriculum designed for classroom settings in grades 9 to 12. The basis of High School FLASH is a public health approach to behavior change. The primary strategy used in the FLASH curriculum for preventing teen pregnancy, sexually transmitted diseases (STDs), and sexual violence is to address student behaviors and attitudes. To this end, FLASH uses a harm reduction and behavior change framework, implements best practices as outlined in the research on effective programs, addresses risk and protective factors for program goals, and rests on the theory of planned behavior. The instructional approach of High School FLASH employs key concepts in every lesson, which enables teachers to hone in on the risk and protective factors outlined in the curriculum logic model. | Behavioural | FLASH curriculum |
| Sexual Health Education for AdolescentsSexual Health Education for Adolescents is a five-session knowledge-based sexual health curriculum designed for classroom settings. The lessons cover the reproductive system, pregnancy, birth control, abstinence, human immunodeficiency virus (HIV) and other sexually transmitted diseases (STDs), and healthy relationships. The goal of the curriculum is to increase student knowledge in all content areas. The primary strategy employed by Sexual Health Education for Adolescents is to address the cognitive learning domain. The curriculum aligns to national health education standards and is intended to be implemented by classroom teachers. The lessons can be delivered according to the schedule that works best for schools (e.g., twice a week, once a week, every days) within a school semester. | Behavioural | Sexual Health Education for Adolescents |
Primary outcome
Self-reported rates of vaginal sex
Time frame: 3 months post-intervention
Measured with a single item required and provided by the funder: "In the past 3 months, have you had vaginal intercourse, even once?" Yes/No
Self-reported rates of vaginal sex
Time frame: 12 months post-intervention
Measured with a single item required and provided by the funder: "In the past 3 months, have you had vaginal intercourse, even once?" Yes/No
Self-reported rates of vaginal sex without a condom or other birth control
Time frame: 3 months post-intervention
Combined the following two questions required and provided by the funder: "In the past 3 months, have you had vaginal intercourse without you or your partner using a condom?" and "In the past 3 months, how many times have you had vaginal intercourse without you or your partner using any of these methods of birth control: birth control pills, the shot, the patch, the ring, intrauterine device (IUD), or Implant" New outcome was coded 'yes' if either question was endorsed and 'no' if both questions were responded to as 'no'
Self-reported rates of vaginal sex without a condom or other birth control
Time frame: 12 months post-intervention
Combined the following two questions required and provided by the funder: "In the past 3 months, have you had vaginal intercourse without you or your partner using a condom?" and "In the past 3 months, how many times have you had vaginal intercourse without you or your partner using any of these methods of birth control: birth control pills, the shot, the patch, the ring, intrauterine device (IUD), or Implant" New outcome was coded 'yes' if either question was endorsed and 'no' if both questions were responded to as 'no'
6 secondary outcomes
Self-reported initiation of vaginal sex
Time frame: 3 months post-intervention
Self-reported initiation of vaginal sex
Time frame: 12 months post-intervention
Self-reported knowledge of sexually transmitted disease (STD) testing
Time frame: 3 months post-intervention
Self-reported knowledge of sexually transmitted disease (STD) testing
Time frame: 12 months post-intervention
Self-reported comfort with family communication regarding sexual health
Time frame: 3 months post-intervention
Self-reported comfort with family communication regarding sexual health
Time frame: 12 months post-intervention
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 11 Sep 2019.
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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.
Karin Coyle, PhD principal investigator
ETR
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing FLASH curriculum and Sexual Health Education for Adolescents in people with Pregnancy Related and Sexual Behavior, 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 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 11 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?
Self-reported rates of vaginal sex (time frame: 3 months post-intervention). The study lists 4 primary outcomes in all. 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 11 Sep 2019.