Facilitated Tucking Position During Endotracheal Suctioning

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

40 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-12-01

Study Completion Date

2023-07-30

Brief Summary

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Aim of the present study The present study will aimed to determine the effect of facilitated tucking position during endotracheal suctioning on physiological criteria and behavioural responses of the preterm neonates.

Research Hypotheses

1. Preterm neonates who receive facilitated tucking position during endotracheal suctioning exhibit more stable physiological criteria than those who do not.
2. Preterm neonates who receive facilitated tucking position during endotracheal suctioning exhibit more stable behavioral responses than those who do not.

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Detailed Description

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Conditions

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Respiratory Distress Syndrome

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

SINGLE

Investigators

Study Groups

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Study Group

Consisted of 20 neonates who will receive tucking position during endotracheal suctioning

Group Type EXPERIMENTAL

tucking position during endotracheal suctioning

Intervention Type PROCEDURE

, the staff nurse will perform the endotracheal suctioning while the researcher will carried out the intervention

Control group

Consisted of 20 neonates who will receive routine care during Endotracheal suctioning

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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tucking position during endotracheal suctioning

, the staff nurse will perform the endotracheal suctioning while the researcher will carried out the intervention

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* Gestational age between 32 and 36 weeks, weight 1200 grams or greater.
* Postnatal age: two days after delivery to allow for resolution of analgesia or anesthesia received by their mothers during labor.
* Have endotracheal intubation.

Exclusion Criteria

* Preterm neonates who have congenital anomalies or neurological malformations, intracranial hemorrhage, seizures.
* Preterm neonates who received sedatives within four hours before the intervention
* Preterm neonates who exposed to any uncomfortable procedure for at least 30 minutes prior to the intervention.

Minimum Eligible Age

32 Weeks

Maximum Eligible Age

36 Weeks

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes