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Clinical Trials/NCT06231485
NCT06231485
Recruiting
Not Applicable

A Randomized Intervention Trial to Increase Access to Reproductive Health Services Among Adolescents and Young Adults With Intellectual and Developmental Disabilities

City University of New York, School of Public Health1 site in 1 country856 target enrollmentOctober 20, 2023

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Knowledge
Sponsor
City University of New York, School of Public Health
Enrollment
856
Locations
1
Primary Endpoint
Proportion who have had a sexual health discussion with medical professional
Status
Recruiting
Last Updated
2 years ago

Overview

Brief Summary

The goal of this clinical trial is to test the effectiveness of a 6-week socialization and sex education curriculum (STEPS2) in young people (aged 16-27 years) with intellectual and developmental disabilities (I/DD), including people with Down syndrome.

The main question it aims to answer is:

Does the STEPS2 health education curriculum increase the proportion of individuals who:

  1. have had a discussion with a medical professional about their sexual health (including sexually transmitted infection testing for those who are sexually active);
  2. know whether they have had the HPV vaccination;
  3. have had the HPV vaccination;
  4. know what sex is; and
  5. know how people get pregnant.

These are the primary outcomes which are being measured one year after study enrollment. Secondary outcomes include knowledge around sexual health and behaviors around contraception and STI prevention among those sexually active at baseline, as well as satisfaction with the intervention.

Participants are randomized to receive either the socialization and sex education curriculum in the experimental group, called the STEPS2 curriculum, or a nutrition and physical exercise curriculum in the comparison group, called Steps To Your Health (STYH).

Participants in the STEPS2 experimental group meet with a health educator in one-on-one individually tailored sessions virtually once a week for one hour for 6 weeks. Participants in the STYH comparison group meet with a health educator in small group sessions of 6-10 participants virtually once a week for one hour for 6 weeks.

Researchers will compare sexual and reproductive health knowledge and behaviors one year after study enrollment to see if the STEPS2 curriculum is effective at increasing knowledge and healthy behaviors.

Detailed Description

The goal of this clinical trial is to test the effectiveness of a 6-week socialization and sex education curriculum (STEPS2) among 856 adolescent and young adults (aged 16-27 years) with mild to moderate intellectual or developmental disabilities (I/DD), including people with Down syndrome. The investigators are recruiting participants through collaboration with the New York State Office of People with Developmental Disabilities (OPWDD), Service Providers, Care Coordination Organizations and special programs, such as the Special Olympics. For participants who meet eligibility criteria and have consented or assented (as appropriate), a video call meeting is arranged to complete the baseline interview survey of socio-demographic characteristics and sexual and reproductive health knowledge and behaviors. The interview takes up to 45 minutes to complete. Once the baseline interview is completed the participant is randomly assigned to either the STEPS2 or the STYH arm of the study. Half of the participants will be randomized to STEPS2, and half to the STYH arm. Participants begin the intervention within 2 weeks of having completed the baseline survey. For the intervention, participants in both arms receive virtual video call one hour weekly health education sessions for 6 weeks. The STEPS2 socialization and sexuality curriculum (experimental arm) is provided during one-on-one sessions between a Study Health Educator and the participant. The STYH curriculum (comparison arm) is provided during group sessions with 6-10 participants and a Study Health Educator. For both arms, participants choose whether they wish for a guardian or helper to also attend for a given session. Participants have follow-up interview surveys at month 2 (after completing the health education intervention), month 6, and month 12, with the same sexual and reproductive health measures as included in the baseline survey. The month 2 interviews also include measures of participant satisfaction with the curriculum and with the Study Health Educator. Each survey takes up to 45 minutes to complete. Survey interviewers are blinded to which curriculum participants have received. The investigators are comparing the proportion of participants who have had a conversation with a doctor about sex, know their HPV vaccination status, have had the HPV vaccine, and show an understanding of sex and pregnancy at the month 12 interview between the two arms, after adjusting for baseline measures of these indicators, to test whether participation in the STEPS2 arm had an effect on these measures. Analysis will include intention-to-treat estimates, as well as instrumental variable estimates to adjust for incomplete attendance to the 6-week curricula. Analyses will also be stratified by gender, age, and mild versus moderate I/DD. If the STEPS2 curriculum is found to improve reproductive and sexual health knowledge and behaviors, the investigators will email the curriculum to all participants in the STYH arm at study completion. Both curricula will be made publicly available at the end of the study.

Registry
clinicaltrials.gov
Start Date
October 20, 2023
End Date
February 2027
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
City University of New York, School of Public Health
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • 16-27 years of age
  • resides in New York State
  • mild/moderate I/DD
  • willing to receive either STEPS2 or STYH curricula
  • able to complete curriculum in English

Exclusion Criteria

  • if female sex, self-reports pregnant at screening

Outcomes

Primary Outcomes

Proportion who have had a sexual health discussion with medical professional

Time Frame: One year post enrollment

Have had a sexual health discussion with medical professional

Proportion who know their HPV vaccination status

Time Frame: One year post enrollment

Know whether they have been vaccinated for HPV

Proportion who have been vaccinated for HPV

Time Frame: One year post enrollment

Have been vaccinated for HPV (self-report with verification using NYS and NYC immunization registry when possible)

Proportion who can accurately describe how a person gets pregnant

Time Frame: One year post enrollment

Can describe that vaginal sex can lead to pregnancy and the general mechanics of how this works in an open-ended question

Proportion who can accurately describe what sex is

Time Frame: One year post enrollment

Understand what sex is based on response to an open-ended question

Secondary Outcomes

  • Proportion using birth control among those reporting vaginal sex(One year post enrollment)
  • Proportion using condoms among those reporting vaginal and/or anal sex(One year post enrollment)
  • Proportion tested for STDs among those reporting vaginal and/or anal sex(One year post enrollment)
  • Average sexual health knowledge score (1-25, with 25 being high knowledge)(Two months post enrollment (after completion of 6 week intervention))
  • Average satisfaction with intervention score (1 to 5, with 5 being very satisfied)(Two months post enrollment (after completion of 6 week intervention))

Study Sites (1)

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