CRUSH curriculum for romance and sexual health for autistic young adults
Official title: A Pilot Investigation of the Competence in Romance and Understanding Sexual Health Curriculum
Run by Boston Children's Hospital · NCT07406100 · Data updated 2026-11-12
This project will try the CRUSH program—a group course plus one-to-one coaching—to teach sexual health and dating skills to autistic adults ages 18 to 30.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years to 30 Years |
| Sex | All |
| Enrollment | 40 (estimated) |
| Sponsor | Boston Children's Hospital Academic / other |
| Locations | 1 site (Brookline, Massachusetts) |
| Status | Recruiting |
| Started | April 1, 2026 |
| Main results expected | July 31, 2027 |
| Study ends | July 31, 2027 |
| Registry record updated | April 24, 2026 |
| Trial ID | NCT07406100 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are autistic adults aged 18 to 30 who are fluent in English, can provide consent, and meet clinical confirmation of autism with cognitive ability sufficient to participate (typically IQ around 70+ or clinician approval).
✕Probably not a fit
People who are non-English-speaking, have a known genetic etiology for autism, have major uncontrolled mental illness, cannot consent, or cannot attend in-person sessions are unlikely to benefit from this pilot.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This pilot interventional program enrolls 40 autistic adults to receive the Competence in Romance and Understanding Sexual Health (CRUSH) curriculum, which combines group-based behavioral sessions with individual coaching across about 20 sessions. Participants are randomized with a waitlist control and complete screening, clinical confirmation of autism features, and three assessment visits before, midway, and after the curriculum to measure knowledge and behaviors related to dating and sexual health. The study will also pilot the measurement battery for use in future trials and explore possible mechanisms of change. Eligibility requires English fluency and the ability to consent, with cognitive level reviewed by a clinician when needed.
Why it matters
Potential benefit: If successful, CRUSH could improve dating skills, sexual health knowledge, and confidence in forming safer intimate relationships for autistic young adults.
How similar studies have gone: This approach is relatively novel for autistic adults—CRUSH was piloted on a small group but there are currently no established evidence-based interventions for dating and sexual health in this population.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * 18;0 to 30;11 years old; * Either documentation of a prior diagnosis of autism spectrum disorder or receipt of services based on an autism spectrum diagnosis OR self identification as being autistic / on the autism spectrum and meeting the clinical cut-off on either the Autism Diagnostic Observation Schedule or the Autism Spectrum Quotient; * Ability to provide consent for the protocol and understand task demands. The Wechsler Abbreviated Scale of Intelligence, Second Edition (WASI-2) may be used to confirm cognitive level. In prior work, adults with full scale IQ of 70 or above on the WASI-2 typically meet this criterion, but a licensed clinician will review individuals who fall below an IQ of 70 on an individual basis to determine eligibility; * Fluent in English. Exclusion Criteria: * Non-English-speaking participants (less than 50% of speech in English); * Known genetic etiology of ASD (e.g., Fragile X); * Major mental illness (e.g., bipolar disorder, schizophrenia, or psychosis); * Medical conditions that impact sexual function (e.g., pituitary tumor); * Significant sensory, motor, or physical conditions that would prevent valid participation in assessments or intervention; * Live more than 50 miles from the site in Brookline, MA where intervention and assessment sessions will be offered. * Receipt of other sexual health/dating curricula as an adult.
Where it's running
-
Boston Children's Hospital, Two Brookline Place
Brookline, Massachusetts, United States Recruiting
Study contacts
- Study coordinator: Susan Faja, PhD
- Email: ProjectCRUSH@childrens.harvard.edu
- Phone: 6179194108
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
AdiaVita and glutathione for autism in kids and teens
This study tests whether adding AdiaVita (cord-blood stem cells and exosomes) to glutathione helps improve ASD symptoms in children and other participants compared with glutathione alone.
-
Online test of BlinkLab Dx1 for autism in kids aged 2–11
This study tests whether the BlinkLab Dx1 smartphone app can help identify autism in children aged 2 to 11 by comparing app-based measurements with prior clinical diagnoses.
-
Gut barrier and gut microbes in children with autism
This trial will test whether a one-month course of postbiotic supplements can improve gut symptoms and behavior in children with autism aged 3–8.
-
Trauma‑Focused Cognitive Behavioral Therapy adapted for autistic children and teens (pilot implementation)
This pilot will try TF‑CBT adapted for autistic children and teens with trauma-related symptoms to see if community mental health clinicians can deliver it and families find it acceptable.
-
Static balance testing in children with autism using a virtual reality system
This project tests whether a virtual reality rehabilitation system can measure static balance differences in children with autism aged 6–10.
-
Virtual reality to improve emotion understanding in children with autism
This project will test whether an Oculus virtual-reality program helps children with autism better recognize and understand emotions compared with a traditional intervention.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.