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Trial · NCT07882199

Efficacy of a Video-based, Parent-centered Home Developmental Intervention for Infants at High Risk for Developmental Delay: a Multicenter Randomized Controlled Trial

NCT07882199, Not applicable, Not yet recruiting, Seoul National University Hospital

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Efficacy of a Video-based, Parent-centered Home Developmental Intervention for Infants at High Risk for Developmental Delay: a Multicenter Randomized Controlled Trial. Trials, record NCT07882199. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07882199

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Efficacy of a Video-based, Parent-centered Home Developmental Intervention for Infants at High Risk for Developmental Delay: a Multicenter Randomized Controlled Trial
NCT number
NCT07882199
Status
Not yet recruiting
Phases
Not applicable
Enrollment
170 participants, estimated
Lead sponsor
Seoul National University Hospital
Conditions
Preterm
Interventions
Family-centered developmental training intervention
First posted
2026-10-20
Last updated
2026-10-20

Source ClinicalTrials.gov

Registered outcomes57

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryBayley-III Motor Composite Scorecorrected age 6 months
This measure assesses the developmental functioning of infants and toddlers. The standard composite scores for each primary domain (Cognitive, Language, and Motor) range from a minimum of 40 to a maximum of 160. Higher scores indicate better developmental performance and a better outcome.
SecondaryGeneral Movement Optimality Score-Revisedbaseline
This observational assessment evaluates the quality of general movements, typically during the writhing movements period in preterm and term infants. The total score ranges from a minimum of 0 to a maximum of 38. Higher scores indicate better quality of movements, representing more optimal motor performance and a better outcome.
SecondaryGeneral Movement Optimality Score-Revisedcorrected age 6 weeks
This observational assessment evaluates the quality of general movements, typically during the writhing movements period in preterm and term infants. The total score ranges from a minimum of 0 to a maximum of 38. Higher scores indicate better quality of movements, representing more optimal motor performance and a better outcome.
SecondaryBayley-III Cognitive Composite Scorecorrected age 6 months
This measure assesses the developmental functioning of infants and toddlers. The standard composite scores for each primary domain (Cognitive, Language, and Motor) range from a minimum of 40 to a maximum of 160. Higher scores indicate better developmental performance and a better outcome.
SecondaryBayley-III Cognitive Composite Scorecorrected age 9 months
This measure assesses the developmental functioning of infants and toddlers. The standard composite scores for each primary domain (Cognitive, Language, and Motor) range from a minimum of 40 to a maximum of 160. Higher scores indicate better developmental performance and a better outcome.
SecondaryBayley-III Cognitive Composite Scorecorrected age 18 months
This measure assesses the developmental functioning of infants and toddlers. The standard composite scores for each primary domain (Cognitive, Language, and Motor) range from a minimum of 40 to a maximum of 160. Higher scores indicate better developmental performance and a better outcome.
SecondaryBayley-III Cognitive Composite Scorecorrected age 24 months
This measure assesses the developmental functioning of infants and toddlers. The standard composite scores for each primary domain (Cognitive, Language, and Motor) range from a minimum of 40 to a maximum of 160. Higher scores indicate better developmental performance and a better outcome.
SecondaryBayley-III Cognitive Composite Scorecorrected age 36 months
This measure assesses the developmental functioning of infants and toddlers. The standard composite scores for each primary domain (Cognitive, Language, and Motor) range from a minimum of 40 to a maximum of 160. Higher scores indicate better developmental performance and a better outcome.
SecondaryMotor Optimality Score-Revisedcorrected age 3 months
This observational tool assesses the concurrent motor repertoire and the quality of fidgety movements in infants, typically between 3 and 5 months of post-term age. The total score ranges from a minimum of 5 to a maximum of 28. Higher scores indicate more optimal motor performance and a better outcome.
SecondaryGross Motor Function Measurecorrected age 6 months
This observational tool evaluates changes in gross motor function. The total score is calculated as a percentage, ranging from a minimum of 0 to a maximum of 100. Higher scores indicate better gross motor function and a better outcome.

Outcomes0

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

None in this release.

Results by group0

Each measurement the trial posted, group by group, in the words and numbers it posted.

None in this release.

Participant flow0

How many started, completed or left each group, period by period.

None in this release.

Adverse events0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

None in this release.

Adverse event totals0

The totals the trial posted for each group.

None in this release.

Papers0

The papers the trial lists on ClinicalTrials.gov.

None in this release.

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

None in this release.

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT07882199

GET https://conductscience.org/api/trials/v1/NCT07882199/registered?page=2