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N/A N=360 Randomized Single-blind Health Services Research

The CHICA Developmental Screening Study

Developmental Delay

Enrolled (actual)
360
Serious AEs
0.0%
Results posted
Jun 2017
Primary outcome: Primary: Number of Children Screened for Developmental Delay — 153; 44 Participants

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
CHICA DevScreen Module (Other)
Age
Pediatric · 0+ yrs
Sex
All
Sponsor
Indiana University
Primary completion
Dec 2012

Outcome Measures

OutcomeResultp-value
PRIMARY
Number of Children Screened for Developmental Delay
153; 44
SECONDARY
Age of Children Diagnosed With Developmental Delay
19.8; 23.8

Summary

The aims of this study are to (1) Expand and modify an existing computer-based decision support system (CHICA) to include the 2006 AAP developmental surveillance and screening algorithm; (2) Evaluate the effect of the CHICA system on the developmental surveillance and screening practices of four pediatric clinics; (3) Evaluate the effect of the CHICA system on referrals for developmental and medical evaluations as well as early developmental intervention/early childhood services for those children identified as having concerning developmental screening results; and (4) Develop a cohort of children with identified developmental disabilities that can be followed over time in order to look at the end results/effects of developmental screening

Eligibility Criteria

Inclusion Criteria

  • This study will involve the analysis of data collected in the care of children seen in four IUMG-PC pediatric clinics. For aim 2 of the study all children between the ages of 0 and 3 seen in the four study clinics will be eligible for and will be participants in the study.

For aim 3 of the study, a child is eligible for participation if they are younger than 5 years of age, have a concerning developmental screening result, and are seen in one of the four clinics participating in this study. Additionally, these children cannot have a previous diagnosis of a developmental disorder and at least one of the child's parents must speak English.

Exclusion Criteria

  • For aim 3, having no parents who can speak English
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01351077). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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