Actively Recruiting

Phase Not Applicable
Age: 6Years - 10Years
All Genders
NCT07476937

Differences in Rest, Emotion, and Arousal Modulation in Youth

Led by University of Pittsburgh · Updated on 2026-05-06

60

Participants Needed

1

Research Sites

221 weeks

Total Duration

On this page

Sponsors

U

University of Pittsburgh

Lead Sponsor

E

Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

Collaborating Sponsor

AI-Summary

What this Trial Is About

The goal of this study is to examine the relationship between sensory responsivity, bedtime arousal levels, sleep disturbances, and daytime emotion dysregulation for autistic children (ages 6-10). In a subset of children with elevated sensory responsivity, a sensory-based bedtime manipulation targeting bedtime arousal levels will be tested.

CONDITIONS

Official Title

Differences in Rest, Emotion, and Arousal Modulation in Youth

Who Can Participate

Age: 6Years - 10Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Youth between the ages of 6 and 10 years old
  • Caregiver-reported autism diagnosis and >11 on Social Communication Questionnaire
  • Caregiver-reported bedtime resistance (>12 on Children's Sleep Habits Questionnaire-Autism; Sleep Initiation subscale - 3-point scale, 6 questions)
  • Caregiver willing to participate in all bedtimes during study
  • Stable medication use (no changes within 2 weeks)
Not Eligible

You will not qualify if you...

  • Does not understand English or unable to travel to the lab in Pittsburgh, PA
  • Diagnosis of sleep apnea, narcolepsy, or major psychiatric disorder (e.g., major depression, bipolar)
  • Unstable medication use (dose or timing)
  • Current behavioral treatment for sleep disorder

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

University of Pittsburgh

Pittsburgh, Pennsylvania, United States, 15219

Actively Recruiting

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Research Team

A

Amy G Hartman, PhD

CONTACT

T

Tracey Y Murray, BS

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

SEQUENTIAL

Primary Purpose

TREATMENT

Number of Arms

2

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