Effectiveness of Home Based Early Intervention of Extremely Premature Infant by Parent

NCT ID: NCT05334550

Last Updated: 2022-06-08

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

110 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-06-02

Study Completion Date

2024-03-02

Brief Summary

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This study is to prove the effectiveness of home based early intervention of extremely premature infant by Parent.

Detailed Description

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The perpose of this study to prove the significance of the hypothesis that there will be a significant improvement in motor development when remote tele-rehabilitation treatment is performed for extremely premature infants. The investigators plan to recruit subjects who meet the inclusion criteria and do not meet the exclusion criteria from among extremely premature infants born at Samsung Hospital, Seoul, Korea, whose gestational age is from 23 weeks to 28 weeks. The target number of n is 110, 55 per group. After randomization into an intervention group and a control group, the intervention group get the intervention starting at 0 months of correctional age and runs for 3 months. In both groups, motor outcomes are measured at the time of enrollment, at 3 months of correction age, 6 months of correction age and 12 months of correction age

Conditions

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Preterm Extreme Prematurity Early Intervention Developmental Delay Motor Outcome Home Exercise Parents

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Outcome Assessors

Study Groups

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Intervention group

Allocated to intervention group through randomization process.

Group Type EXPERIMENTAL

Home Based Early Intervention by Parent

Intervention Type OTHER

Through a video communication program called ZOOM, the parents of intervention group are educated once every two weeks for three months. Parent education consists of a program developed by our pediatric rehabilitation therapist to help premature infants develop motor skills. Parents provide daily exercise training to their children as educated.

Control group

Allocated to control group through randomization process.

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Home Based Early Intervention by Parent

Through a video communication program called ZOOM, the parents of intervention group are educated once every two weeks for three months. Parent education consists of a program developed by our pediatric rehabilitation therapist to help premature infants develop motor skills. Parents provide daily exercise training to their children as educated.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Extreme premature baby (gestationl age 23\~28 weeks)
* Corrected age under one month at the time of enroll of this study
* Children of those who voluntarily decided to participate after hearing detailed explanations about this study and gave their written consent.
* Children whose parents are Korean

Exclusion Criteria

* Congenital anomalies in the central nervous system
* Hereditary diseases
* Chromosomal abnormalities (Down syndrome, etc.)
* Stage 3 or more intraventricular hemorrhage
* If surgery was performed for hydrocephalus
* Leukomalacia confirmed by ultrasound examination (not applicable to increase in white matter shading)
* Neonatal asphyxia
* Other central nervous system diseases
* If taking medications for convulsions or epilepsy
* Metabolic disease
* In the case of premature infants undergoing surgery for retinal disease
* Hearing loss
* In case of surgery due to complex congenital anomaly or planned operation (not excluded if surgery is not required)
* In case of oxygen dependence due to lung disease in premature infants
* Musculoskeletal disorders (hip dislocation, polyarthrosis, etc.)
* Neuromuscular disease, etc.
* Those whose family has social problems
* Those whose parents cannot participate in this study
* Those who have other serious complications that cannot proceed with the study
Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Samsung Medical Center

OTHER

Sponsor Role lead

Responsible Party

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Jeong Yi Kwon

Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Kwon Jeong-Yi, PhD

Role: PRINCIPAL_INVESTIGATOR

Samsung Medical Center

Central Contacts

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Lee Jinuk, resident

Role: CONTACT

+8210-4555-3349

Kwon Jeong-Yi, PhD

Role: CONTACT

+82-2-3410-2818

References

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통계청, 『2019년 출생통계(확정), 국가승인통계 제10103호 출생통계』

Reference Type BACKGROUND

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Reference Type BACKGROUND

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Reference Type BACKGROUND
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Reference Type BACKGROUND
PMID: 8250792 (View on PubMed)

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Reference Type BACKGROUND
PMID: 1468050 (View on PubMed)

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Reference Type BACKGROUND

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Other Identifiers

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2022-02-28

Identifier Type: -

Identifier Source: org_study_id

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