Skip to main content
OpenTrials
Recruiting

NCT Number: NCT05501678

Trial of Diphenhydramine for Sleep in Children With Autism

The purpose of this study is to examine the effect of diphenhydramine on sleep in children and adolescents with Autism Spectrum Disorder (ASD). Diphenhydramine is an anti-histaminergic agent with strong hypnotic properties. To accomplish this, the investigators will use a randomized double-blind placebo-controlled crossover 8-week study design to examine the effect of diphenhydramine on sleep physiology as assessed by polysomnography (PSG), actigraphy, circadian rhythm, and clinical measures.

Recruiting

Interested in participating?

Request Info

Key information

Age range

8 year–17 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Participants will meet the following

  • Outpatients between 8 and 17 years of age at the time of consent
  • Diagnostic and Statistical Manual, 5th edition (DSM-5) criteria for Autism Spectrum Disorder (ASD) on the basis of clinical evaluation, confirmed with the Autism Diagnostic Interview-Revised (ADI-R) and the Autism Diagnostic Observation Schedule, 2nd Ed (ADOS-2) or the Childhood Autism Rating Scale, Second Edition (CARS-2).
  • Males and females
  • Availability of polysomnography (PSG) or actigraphy data
  • Sleep disturbances as assessed using Children's Sleep Habits Questionnaire (CSHQ) with a score of 41 or higher
  • care provider who can reliably bring participant to clinic visits, provide trustworthy ratings, and interacts with participant on a regular basis
  • stable medications for at least 2 weeks, with the exception of Prozac which is required to be stable for at least 4 weeks
  • no planned changes in psychosocial and biomedical interventions during the trial
  • willingness to provide additional saliva samples and participate in key study procedures (i.e., safety measurements every visit, PSG at weeks 4 and 8, and wear the actigraphy watch for 2 weeks before the beginning of trial as well as during the 8 weeks of the trial).

Exclusion criteria

Participants will be excluded if one or more of the following is met

  • active suicidal ideation or DSM-5 diagnosis of schizophrenia, schizoaffective disorder, or psychotic disorder
  • active medical problems: migraine, asthma, seizure disorder, significant physical illness (e.g., anaphylaxis, serious liver, renal, or cardiac pathology)
  • evidence of a metabolic, or infectious etiology for the participant's autism on the basis of medical history, neurologic history, and available tests for inborn errors of metabolism and chromosomal analysis
  • pregnant or sexually active females not using a reliable method of contraception (urinary tests for pregnancy will be employed in this study)
  • individuals taking benzodiazepines, antiepileptic medications when prescribed for seizure disorder/epilepsy, melatonin and centrally-acting antihistamines
  • history of hypersensitivity to diphenhydramine
  • history of severe side effects from diphenhydramine
  • history of adequate trial of diphenhydramine
  • current use of any medications known to interact with diphenhydramine such as medications inhibiting CYP2D6
  • taking anticholinergic agents (e.g., trihexyphenidyl, thioridazine).

Treatment and study plan

diphenhydramine

Drug

25mg (and up to 50mg) Diphenhydramine given orally

Other names: Benadryl

Placebo

Drug

Matching Placebo given orally

Primary outcomes

  1. Change from baseline in sleep latency as measured by polysomnography (PSG) and/or actigraphy

    Time frame: Baseline, Week 4 and Week 8

  2. Change from baseline in duration of non-rapid eye movement (NREM) sleep as measured by polysomnography (PSG)

    Time frame: Baseline, Week 4 and Week 8

Secondary outcomes

  1. Change from baseline in sleep efficiency as measured by polysomnography (PSG) and actigraphy

    Time frame: Baseline, Week 4 and Week 8

Other outcomes

  1. Change from baseline on Children's Sleep Habits Questionnaire (CSHQ) subscale scores

    Time frame: Baseline, Week 4, Week 8

  2. Change from baseline on Aberrant Behavior Checklist, Second Edition (ABC-2) subscale scores

    Time frame: Baseline, Week 4, Week 8

  3. Change from baseline on Parent Sleep Habits Questionnaire Parent (PSHQ) scores

    Time frame: Baseline, Week 4, Week 8

  4. Change from baseline on Clinical Global Impression Scale (CGI) scores

    Time frame: Baseline, Week 1, Week 2, Week 3, Week 4, Week 5, Week 6, Week 7, and Week 8

  5. Change from baseline on Child Behavior Checklist (CBCL) scores

    Time frame: Baseline, Week 4, Week 8

  6. Change from baseline on Social Responsiveness Scale, Second Edition (SRS-2) scores

    Time frame: Baseline, Week 4, Week 8

  7. Change from baseline on Repetitive Behavior Scale - Revised (RBS-R) scores

    Time frame: Baseline, Week 4, Week 8

  8. Change from baseline on Sensory Profile Questionnaire (SPQ) scores

    Time frame: Baseline, Week 4, Week 8

  9. Change from baseline on Stanford Social Dimension Scale (SSDS) scores

    Time frame: Baseline, Week 4, Week 8

  10. Change from baseline on Dimensional Assessment of Repetitive Behaviors (DARB) scores

    Time frame: Baseline, Week 4, Week 8

  11. Change from baseline on NEuroPSYchological Assessment, 2nd Edition (NEPSY-2) Affect Recognition scores

    Time frame: Baseline, Week 4, Week 8

Study contacts

Contact information is provided by the study sponsor or research team.

Robin Libove

CONTACT

[email protected]

(650)736-1235

Ryan Villacrucis

CONTACT

[email protected]

(650)736-1235

Sponsors and collaborators

Lead sponsor

Stanford University

Other

Collaborators

  • National Institutes of Health (NIH)

Registry information

Official study title

Randomized Placebo-controlled Crossover Trial of Diphenhydramine for Sleep in Children With Autism

Important dates

Study start
2023
Primary completion
2027
Study completion
2027
First posted
Aug 15, 2022
Registry last updated
Mar 27, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.