Actively Recruiting

Phase Not Applicable
Age: 3Years - 6Years
All Genders
NCT07532395

FMS-CrossFit Training Program (FCTP) to Improve School Readiness in Preschool Children With Autism Spectrum Disorder

Led by Peking University · Updated on 2026-05-11

184

Participants Needed

1

Research Sites

74 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Autism spectrum disorder (ASD) is an increasing public health concern, with preschool children often exhibiting persistent deficits in school readiness. However, targeted and developmentally comprehensive interventions remain limited. This randomized controlled trial will evaluate a 12-week Fundamental Movement Skills-CrossFit Training Program (FCTP) in 184 children with ASD aged 3-6 years, compared with a Treatment As Usual (TAU) control group. The program integrates progressive FMS training with CrossFit-style circuit training to improve motor competence, social interaction, and self-regulation. Primary outcomes focus on school readiness assessed by the Strengths and Difficulties Questionnaire (SDQ), while secondary outcomes include motor development, executive function, social responsiveness, and biomarkers. Assessments will be conducted at baseline, mid-intervention (8 weeks), post-intervention (12 weeks), and follow-up (20 weeks).

CONDITIONS

Official Title

FMS-CrossFit Training Program (FCTP) to Improve School Readiness in Preschool Children With Autism Spectrum Disorder

Who Can Participate

Age: 3Years - 6Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age between 3 and 6 years
  • Confirmed diagnosis of Autism Spectrum Disorder by DSM-5 or ADOS-2
  • Ability to understand basic verbal instructions
  • Written informed consent provided by parent or caregiver
Not Eligible

You will not qualify if you...

  • Participation in structured exercise programs during the past 6 months
  • Severe neurological disorders (e.g., epilepsy, phenylketonuria, fragile X syndrome, tuberous sclerosis)
  • Major psychiatric conditions (e.g., schizophrenia, bipolar disorder)
  • Visual, auditory, or intellectual impairments interfering with participation
  • History of significant head trauma or brain injury
  • Medical conditions that prevent physical activity
  • Other factors deemed unsuitable by the research team

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Fujian Provincial Maternity and Children's Hospital

Fuzhou, Fujian, China, 350001

Actively Recruiting

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Research Team

Y

Yuelong Ji, PHD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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