Randomized Evaluation of a Multi-Component, Rights-Based Sexuality Education Initiative for High School Students (SEI)

November 1, 2018 updated by: Public Health Institute, California
This study examines the effectiveness of the Sexuality Education Initiative (SEI), a comprehensive, multi-component, rights-based sexuality education program developed and implemented by Planned Parenthood Los Angeles for high school students. The primary goal of the SEI is to improve the sexual and reproductive health of youth attending Los Angeles high schools. The SEI consists of four intervention components: (1) a 12-session gender-sensitive, rights-based, comprehensive sexuality education curriculum, (2) a peer education and advocacy component, (3) a parent education component, and (4) clinical services linkages. It is hypothesized that the 12-session classroom curriculum is more effective than a 3-session control sex education curriculum. It is also hypothesized that the full SEI package (all four components) is more effective than the control condition (control curriculum and clinical services only).

Study Overview

Detailed Description

This study examines the effectiveness of the Sexuality Education Initiative (SEI), a comprehensive, multi-component, rights-based sexuality education program developed and implemented by Planned Parenthood Los Angeles for high school students. The primary goal of the SEI is to improve the sexual and reproductive health of youth attending Los Angeles high schools. The SEI consists of four intervention components: (1) a 12-session gender-sensitive, rights-based, comprehensive sexuality education curriculum, (2) a peer education and advocacy component, (3) a parent education component, and (4) clinical services linkages.

  • The 12-session gender-sensitive, rights-based classroom curriculum covers anatomy, abstinence, contraception and protection, STIs and HIV/AIDS, media messages, gender, relationships, rights and responsibilities, pregnancy, sexuality, peer pressure, negotiation and coercion, and decision making.
  • The peer education and advocacy component recruits, trains and supervises students through an after-school leadership program to serve as school-wide resources to their peers, organize health events at school, and refer students to school-based clinic services.
  • The parent education component consists of a series of sessions for parents, covering reproductive health, teen pregnancy, and parent-teen communication, together with a parent education booklet for widespread use.
  • The in-school clinical services component provides "clinic without walls" health services on campus, including pregnancy and STI testing, contraceptive consultation and prescriptions, condom distribution, counseling, and referrals. It also trains teachers and school staff to distribute condoms to students as needed.

The evaluation design involves two levels of randomization: First, all schools are randomized into one of two conditions: receiving all three SEI school wide components (peer, parent, clinical services) or receiving only one of these three school wide components (clinical services). Schools are randomized within matched pairs of demographically similar schools. Second, within each school, classrooms are randomized into one of two conditions: a basic 3-session sex education curriculum (control) or the 12-session SEI curriculum (intervention). Thus, all participating 9th grade students will receive at least three sexuality education curriculum sessions and access to on-site clinic services.

The primary research questions for the evaluation are:

  1. Is the 12-session SEI gender-sensitive, rights-based sexuality education curriculum more effective than a 3-session comparison curriculum in reducing risk of unwanted pregnancy and sexually transmitted infections (STIs) among high school students?
  2. Is the full comprehensive program (all four components as a package) more effective than the two-component comparison condition (only the 3-session comparison curriculum and the clinical services linkages) in reducing risk of teen pregnancies and STIs?

The first hypothesis is that the 12-session SEI gender-sensitive, rights-based curriculum is more effective than the 3-session comparison curriculum in improving sexual health outcomes (as defined in section 7) among program participants one year after participation in the program. The second hypothesis is that the full SEI program (all four components as a package) is more effective than the comparison condition (only the 3-session comparison curriculum and the clinical services linkages) in improving sexual health outcomes one year after participation.

In addition to addressing these questions using the designated primary and secondary outcomes, this study will examine changes in the following short-term outcomes that measure critical concepts being addressed by the curriculum and serve as the hypothesized mediators in the SEI theory of change:

  • Attitudes about rights in sexual relationships
  • Communication about relationships, rights and sexuality with partners
  • Communication about relationships, rights and sexuality with parents/ guardians
  • Access to accurate information about sexuality and sexual health
  • Knowledge about sex, sexuality and sexual risk protection
  • Self-efficacy to assert sexual limits and manage risky situations
  • Intentions to protect self from sexual risk
  • Awareness of sexual and reproductive health services

Study Type

Interventional

Enrollment (Actual)

1909

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • California
      • Los Angeles, California, United States, 90007
        • Planned Parenthood Los Angeles

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

13 years to 16 years (Child)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • 9th grade student at a participating high school in East or South Los Angeles
  • Written parent/guardian consent and student assent to participate

Exclusion Criteria:

  • None

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

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
Experimental: SEI Classroom Curriculum
Participants receive the SEI classroom curriculum.
Participants receive the 12-session Sexuality Education Initiative (SEI) classroom curriculum. The SEI classroom curriculum covers anatomy, abstinence, contraception and protection, STIs and HIV/AIDS, media messages, gender, relationships, rights and responsibilities, pregnancy, sexuality, peer pressure, negotiation and coercion, and decision making. These sessions are delivered over a two-month period. Each curriculum session is about 45 minutes in length.
Active Comparator: Control Classroom Curriculum
Participants receive the control classroom curriculum.
Participants receive the 3-session basic control curriculum. The control curriculum includes 3 sessions on sexually transmitted infections, anatomy and birth control delivered over a two- or three-week period. Each curriculum session is about 45 minutes in length.
Experimental: SEI Curriculum + 3 School Components
Participants receive SEI classroom curriculum and three school wide components (peer advocacy and education, parent education, clinical services linkages).
Participants receive SEI classroom curriculum and all three school wide components. The peer education/advocacy component recruits, trains and supervises students through an after-school leadership program to serve as resources to peers, organize health events, and refer students to school-based clinic services. The parent education component provides sessions for parents of students, covering reproductive health, teen pregnancy, and parent-teen communication, together with a parent education booklet for widespread use. The clinical services linkages includes health services on campus, including pregnancy/STI testing, contraceptive consultation and prescriptions, condom distribution, counseling, and referrals. It includes training for teachers and staff to distribute condoms as needed.
Active Comparator: Control Curriculum + 1 School Component
Participants receive control classroom curriculum and one of the three school wide components (clinical services linkages).
Participants receive control classroom curriculum and one of the three school wide components, the clinical services linkages. This component includes health services on campus for students, including pregnancy and STI testing, contraceptive consultation and prescriptions, condom distribution, counseling, and referrals. It also includes training for teachers and school staff to distribute condoms to students as needed.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Percent of Participants With Pregnancy Risk
Time Frame: 1 year
Between-arm difference in percent of youth who report engaging in recent sexual intercourse but not using birth control and/or condoms
1 year
Percent of Participants With Sexually Transmitted Infection (STI) Risk
Time Frame: 1 year
Between-arm difference in percent of youth who report engaging in recent vaginal, anal and/or oral sexual intercourse but not using condoms
1 year
Percent of Participants With Multiple Sexual Partners
Time Frame: 1 year
Between-arm difference in percent of youth who report having more than one recent vaginal, anal and/or oral sexual partner
1 year
Percent of Participants Who Ever Used Sexual and Reproductive Health Services
Time Frame: 1 year
Between-arm difference in percent of youth who report ever using sexual and reproductive health services
1 year

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Percent of Participants Who Ever Had Sex
Time Frame: 1 year
Between-arm difference in percent of youth who report ever engaging in vaginal and/or anal sexual intercourse
1 year
Percent of Participants Who Ever Had Oral Sex
Time Frame: 1 year
Between-arm difference in percent of youth who report ever engaging in oral sexual intercourse
1 year
Percent of Participants With Recent Sexual Activity
Time Frame: 1 year
Between-arm difference in percent of youth who report engaging in vaginal and/or anal sexual intercourse during the last 3 months
1 year
Percent of Participants With Recent Oral Sex Activity
Time Frame: 1 year
Between-arm difference in percent of youth who report engaging in oral sexual intercourse in the last 3 months
1 year
Percent of Participants Who Used Condom at Last Sex
Time Frame: 1 year
Between-arm difference in percent of youth who report using a condom the last time they had sexual intercourse
1 year
Percent of Participants Who Used Contraceptive at Last Sex
Time Frame: 1 year
Between-arm difference in percent of youth who report using birth control and/or condoms the last time they had sexual intercourse
1 year
Percent of Participants Who Currently Have Condom
Time Frame: 1 year
Between-arm difference in percent of youth who report currently having a condom with them (e.g., in a pocket, purse or backpack)
1 year

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Norman A. Constantine, PhD, Public Health Institute
  • Principal Investigator: Louise A. Rohrbach, PhD, MPH, University of Southern California

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

September 1, 2011

Primary Completion (Actual)

May 1, 2014

Study Completion (Actual)

May 1, 2014

Study Registration Dates

First Submitted

November 18, 2013

First Submitted That Met QC Criteria

December 6, 2013

First Posted (Estimate)

December 11, 2013

Study Record Updates

Last Update Posted (Actual)

November 29, 2018

Last Update Submitted That Met QC Criteria

November 1, 2018

Last Verified

November 1, 2018

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

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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