Application of the Best Evidence of Neonatal Individualized Developmental Care Assessment Program (NIDCAP) in Very Low Birth Weight Infant (VLBWI)

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

COMPLETED

Clinical Phase

NA

Total Enrollment

14 participants

Study Classification

INTERVENTIONAL

Study Start Date

2021-03-01

Study Completion Date

2022-03-01

Brief Summary

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In order to help THE GROWTH and development of VLBWI in Neonatal Intensive Care Unit (NICU) and reduce the interference of external environment to them, we summarized the best evidence of NIDCAP care, and applied the evidence to the intervention group, and observed the compliance of nurses in the intervention group to the application of evidence, and the short-term outcomes of VLBWI.

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Detailed Description

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Conditions

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NIDCAP

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

SINGLE

Outcome Assessors

Study Groups

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NIDCAP care

The training core group was formed by the project team. After a one-month clinical unified training on the best evidence of NIDCAP for the VLBW nursing professional group, the best evidence of NIDCAP was applied to the intervention group.

Group Type EXPERIMENTAL

NIDCAP care

Intervention Type BEHAVIORAL

NIDCAP care was performed according to the best evidence of NIDCAP

routine nursing care

routine nursingPerform routine care for NICU infants according to the nursing routine of each hospital

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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NIDCAP care

NIDCAP care was performed according to the best evidence of NIDCAP

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* Birth weight \<1500g;
* admit within 24 hours of birth;
* The guardian signs the informed consent;
* OI (oxygenation index \>300)

Exclusion Criteria

* Newborn with severe congenital malformations or various chromosomal diseases, genetic metabolic diseases, severe neurological diseases;
* Newborn who did not achieved discharge or death at the end of the study period

Maximum Eligible Age

1 Day

Eligible Sex

ALL

Accepts Healthy Volunteers

No