Clin2
NCT03836300Possibly a fitEnrolling by invitation

Parent-infant coaching for families with young diagnoses

Fragile X SyndromeAngelman SyndromePrader-Willi SyndromeDup15Q SyndromeDuchenne Muscular DystrophyPhelan-McDermid SyndromeRett SyndromeSmith Magenis Syndrome

Part of Blood & lymphatic, Bones, joints & muscles, Brain & nervous system, Cancer, Genetic & congenital, Heart & circulation, Hormones & metabolism, Kidney & urinary, Mental health, Women’s health & pregnancy clinical trials.

This study tests a parent-and-infant coaching program for babies and caregivers. It aims to see whether the program helps after an early diagnosis when English is used at home.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
120 people
Ages
Up to 99 years
Study type
Interventional

Who can take part

  • Your baby is 15 months old or younger.
  • Your baby has had a diagnosis that was not only because a parent was worried (for example, it came from prenatal or newborn screening, or from family testing).
  • English is the main language spoken at home, because the study activities and questionnaires are in English.
  • Your baby can take part in the study with normal vision (the study is not set up for blind infants).
  • Your baby does not have severe hearing loss (the study requires hearing to follow the activities and assessments).

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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