Kangroo Mother Care

NCT ID: NCT05955404

Last Updated: 2023-07-21

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

21 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-11-02

Study Completion Date

2023-02-28

Brief Summary

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infants had a condition that might influence their responses to pain, e.g., congenital anomalies or severe illnesses requiring treatment with antiepileptics, muscle relaxants, or analgesic drugs.

Detailed Description

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infants had a condition that might influence their responses to pain, e.g., congenital anomalies or severe illnesses requiring treatment with antiepileptics, muscle relaxants, or analgesic drugs and comparing the pain intensity with preterm infants who receive conventional care.

Conditions

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Preterm Birth Complication

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

This study uses the Kangaroo mother care as a non-pharmacological strategy to alleviate the pain that preterm infants experience in the NICU.
Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

NONE

Study Groups

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Kangaroo mother care

This study uses the Kangaroo mother care as a non-pharmacological strategy to alleviate the pain that preterm infants experience in the NICU.

Group Type EXPERIMENTAL

Kangaroo mother care

Intervention Type OTHER

This study uses the Kangaroo mother care as a non-pharmacological strategy to alleviate the pain that preterm infants experience in the NICU.

Interventions

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Kangaroo mother care

This study uses the Kangaroo mother care as a non-pharmacological strategy to alleviate the pain that preterm infants experience in the NICU.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Preterm infants whose corrected gestational age from (32 - \<37) weeks of pregnancy
* Preterm infants who do not experience any painful procedure for last 24 hours
* Preterm infants do not receive any sedation for last 24 hours

Exclusion Criteria

* full-term infants whose corrected gestational age is \>37 weeks
* extremely preterm (\< 28 weeks)
* very preterm (28-\<32 weeks)
* proven or suspected sepsis
* major congenital malformations
* all heart defect except neonatal Patent ductus arteriosus (PDA)
* necrotizing enterocolitis
* neurodevelopmental disability
* who receive respiratory support {Mechanical Ventilation, Continuous Positive Airway Pressure, or high-flow support
* indicated for surgery
* contraindication to oral sucrose
* Twins
* infants had a condition that might influence their responses to pain, e.g., congenital anomalies or severe illnesses requiring treatment with antiepileptics, muscle relaxants, or analgesic drugs
Minimum Eligible Age

32 Weeks

Maximum Eligible Age

37 Weeks

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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University of Baghdad

OTHER

Sponsor Role lead

Responsible Party

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Hiba Abdulwahid Dawood

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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College of Nursing- The University of Baghdad

Baghdad, , Iraq

Site Status

Countries

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Iraq

Other Identifiers

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kangroo mother care

Identifier Type: -

Identifier Source: org_study_id

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