Actively Recruiting

Age: 6Months - 24Months
All Genders
Healthy Volunteers
NCT07011082

Hair Biomarkers Study

Led by Stanford University · Updated on 2025-06-24

600

Participants Needed

1

Research Sites

262 weeks

Total Duration

On this page

Sponsors

S

Stanford University

Lead Sponsor

E

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

Collaborating Sponsor

AI-Summary

What this Trial Is About

Young children aged 0-4 years may be exposed to adverse childhood experiences (ACEs) and/or early life adversity (ELA), which are linked with worse physical and mental health across their lifespan. On the other hand, positive childhood experiences (PCEs) can build resilience and prevent or protect against these detrimental outcomes. Data analyses will assess the interactions of ACEs, PCEs, parenting, and poverty on the early social psychology of childhood and develop objective measures for altered stress regulation using hair cortisol as a chronic stress biomarker.

CONDITIONS

Official Title

Hair Biomarkers Study

Who Can Participate

Age: 6Months - 24Months
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Children aged 6 months to 24 months who are healthy as defined by the American Academy of Pediatrics
  • Living in Santa Clara, San Mateo, or Alameda Counties in Northern California
  • Willing to provide a home address to receive study kits
  • Committed to follow-up visits every 6 months for 2 years
Not Eligible

You will not qualify if you...

  • Children with scalp conditions like tinea capitis, alopecia areata, eczema, or dermatitis
  • Children who had systemic steroid therapy in the 3 months before joining the study
  • Children using prescription drugs that affect cortisol or stress hormones for 2 weeks or longer in the past 3 months
  • Children with chronic diseases such as cystic fibrosis, sickle cell disease, asthma, eczema, or other chronic illnesses
  • Children with developmental delays, chromosomal anomalies, seizure disorders, cerebral palsy, chronic pain, or disabilities
  • Children whose hair was chemically treated (dyeing, bleaching, straightening, perming) within 90 days before enrollment or before each follow-up visit during the study period

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

Stanford University

Palo Alto, California, United States, 94304

Actively Recruiting

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Research Team

K

Kanwaljeet J.S. Anand, MBBS, DPhil

CONTACT

C

Cynthia R Rovnaghi, PhD

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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