CClinicalTrials.gg
RecruitingNCT06231485STEPS2Updated Jan 30, 2024

Socialization To Enrich Participation & Support Sexuality for Young People With I/DD

An interventional study of STEPS2 and STYH in Knowledge and Behavior, sponsored by City University of New York, School of Public Health. Recruiting at 1 site in United States. Open to participants aged 16 Years to 27 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2024-01-30.

Sponsored by City University of New York, School of Public Health · Not applicable, Interventional, and Other

From the registry’s dates

  • Started Oct 2023; still recruiting 2 years 11 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
856
Allocation
Randomized
Ages
16 Years to 27 Years
Sex
All
01

Study 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.

Read the 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.

02

Conditions studied

  • Knowledge
  • Behavior
03

In context

Lead sponsor

City University of New York, School of Public Health is the lead sponsor of 14 studies on the registry; 4 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
16 Years to 27 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

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

Exclusion Criteria:

  • if female sex, self-reports pregnant at screening
05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
856 participants (estimated)

Study arms

  • Experimental
    Socialization and sex education (STEPS2)

    Weekly virtual one hour one-on-one sessions with Study Health Educator on the STEPS2 curriculum for 6-weeks. Topics include: the human body, decision-making, sexually transmitted diseases, pregnancy, birth control, pregnancy and parenting, and going to the doctor.

    Behavioral: STEPS2

  • Other
    Nutrition and physical activity (STYH)

    The comparison curriculum has been shown in a previous study to improve knowledge around nutrition and exercise, but should not change sexual and reproductive health outcomes. Weekly virtual one hour group sessions (6-10 participants) with Study Health Educator on the Steps To Your Health (STYH) curriculum for 6-weeks. Topics include: nutrition, exercise, stress management, changing your way of thinking, and behaviors to stay healthy.

    Behavioral: STYH

Interventions

  • BehavioralSTEPS2

    One of the two health education curricula as described in arm/group descriptions.

  • BehavioralSTYH

    One of the two health education curricula as described in arm/group descriptions.

06

What researchers measure

Primary outcomes

  1. Proportion who have had a sexual health discussion with medical professional

    Have had a sexual health discussion with medical professional

    Time frame: One year post enrollment

  2. Proportion who know their HPV vaccination status

    Know whether they have been vaccinated for HPV

    Time frame: One year post enrollment

  3. Proportion who have been vaccinated for HPV

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

    Time frame: One year post enrollment

  4. Proportion who can accurately describe what sex is

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

    Time frame: One year post enrollment

  5. Proportion who can accurately describe how a person gets pregnant

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

    Time frame: One year post enrollment

Secondary outcomes

  1. Average sexual health knowledge score (1-25, with 25 being high knowledge)

    Score based on sexual health knowledge survey questions

    Time frame: One year post enrollment

  2. Average sexual health knowledge score (1-25, with 25 being high knowledge)

    Score based on sexual health knowledge survey questions

    Time frame: 6 months post enrollment

  3. Average sexual health knowledge score (1-25, with 25 being high knowledge)

    Score based on sexual health knowledge survey questions

    Time frame: Two months post enrollment (after completion of 6 week intervention)

  4. Proportion using birth control among those reporting vaginal sex

    Self-reported use of birth control among those reporting vaginal sex

    Time frame: One year post enrollment

  5. Proportion using condoms among those reporting vaginal and/or anal sex

    Self-reported use of condoms among those reporting vaginal and/or anal sex

    Time frame: One year post enrollment

  6. Proportion tested for STDs among those reporting vaginal and/or anal sex

    Self-reported STD testing among those reporting vaginal and/or anal sex

    Time frame: One year post enrollment

  7. Average satisfaction with intervention score (1 to 5, with 5 being very satisfied)

    Average of self-reported satisfaction with 1. curriculum, 2. health educator and 3. participant manual (on a scale of 1 to 5 for each question)

    Time frame: Two months post enrollment (after completion of 6 week intervention)

07

Study locations

1 of 1 sites recruiting
08

References and documents

Individual participant data

Plan to share: Yes — Anonymized survey data from baseline, month 2, 6 and 12 will be made available for other researchers.

Supporting information: Study protocol, Sap, Icf, Analytic code

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 30, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06231485
Lead sponsor
City University of New York, School of Public Health
Collaborators
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), National Institutes of Health INCLUDE Project, National Institutes of Health Office of Disease Prevention
Responsible party
Sponsor
First posted
Jan 30, 2024
Start date
Oct 20, 2023
Primary completion
Feb 2027 (estimated)
Completion
Feb 2027 (estimated)
Last update
Jan 30, 2024

Study contacts

Heidi E Jones, PhD
Contact
heidi.jones@sph.cuny.edu
646-364-9529
Suzanne McDermott, PhD
Contact
suzanne.mcdermott@sph.cuny.edu
Suzanne McDermott, PhD
principal investigator · CUNY School of Public Health
Heidi E Jones, PhD
principal investigator · CUNY School of Public Health

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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