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CompletedNCT05408351Updated Jun 9, 2022

The Indonesian Version of Ages and Stages Questionnaire III Accuracy Compared to Bayley Scales of Infant Development III

An observational study in Child Development, Child Development Disorder and Development Delay, sponsored by Universitas Indonesia. Completed at 1 site in Indonesia. Open to participants aged 23 Months to 38 Months, including healthy volunteers. Per ClinicalTrials.gov, last updated 2022-06-09.

Sponsored by Universitas Indonesia · Observational

Study type
Observational
Model
Ecologic or community
Time perspective
Cross-sectional
Enrollment
131
Ages
23 Months to 38 Months
Sex
All
01

Study summary

This study aimed to evaluate the concurrent validity information of the 24-, 30-, and 36-month Indonesian ASQ-3 with the Bayley Scales of Infant and Toddler Development 3rd Edition (BSID-III) in Indonesian children. Children living in Tanah Tinggi subdistrict, Central Jakarta, were recruited conveniently from November to December 2019. Children within the 24-, 30-, or 36-month age group were assessed for Indonesian ASQ-3 concurrently with BSID-III as the reference standard according to their age groups. Screening test accuracy was measured in sensitivity, specificity, and predictive values for both overall dan specific domains.

02

Conditions studied

  • Child Development
  • Child Development Disorder
  • Development Delay
  • Developmental Delay
  • Global Developmental Delay
  • Motor Delay
  • Speech Delay

Keywords

  • ASQ-3
  • BSID-III
  • child development
  • Indonesia
  • screening test
  • validity
03

In context

Developmental Disabilities

291 studies on the registry are indexed under Developmental Disabilities; 65 are open to participants now.

This study's enrollment of 131 is below the median of 150 across 83 observational studies indexed under Developmental Disabilities.

Browse Developmental Disabilities studies →

Lead sponsor

Universitas Indonesia is the lead sponsor of 29 studies on the registry; 12 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
23 Months to 38 Months
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Probability sample

Study population

Parents with children aged 23-38 months living in Central Jakarta.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Parents with children aged 23 - 38 months
  • Parents who finished at least elementary school

Exclusion criteria

Exclusion Criteria:

  • Parents with communication difficulties
  • Parents who could not speak Indonesian language
05

Study design

Observational model
Ecologic or community
Time perspective
Cross-sectional
Enrollment
131 participants (actual)
Patient registry
No
06

What researchers measure

Primary outcomes

  1. Child development

    Measured once with Indonesian Ages and Stages-3 questionnaire (cross sectional study) with scores ranging between 0 to 60 per domain. Higher score means better development.

    Time frame: Day 1

  2. Child development

    Measured once with Bayley Scales Infant Development-III with scores ranging between 40 to 160 per domain. Higher score means better development.

    Time frame: Day 1

07

Study locations

1 site
  • Tanah Tinggi subdistrict community health centers
    Jakarta Pusat, 10430, Indonesia
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Ran from Nov 2019 to primary completion in Dec 2019, 1 month.

How these figures are worked out, and which studies are left out of them.

Registered
May 25, 2022
First posted
Jun 7, 2022
StartActual
Nov 1, 2019
Primary completionActual
Dec 31, 2019
CompletionActual
Dec 31, 2019
Last update
Jun 9, 2022
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Jun 9, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05408351
Lead sponsor
Universitas Indonesia
Responsible party
Prof. Hartono Gunardi, MD, PhD (Professor, Universitas Indonesia) — Principal investigator
First posted
Jun 7, 2022
Start date
Nov 1, 2019
Primary completion
Dec 31, 2019
Completion
Dec 31, 2019
Last update
Jun 9, 2022

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jun 2022. You cannot join it, but the record below documents what was studied.

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Discussion

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