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CompletedNCT02919540Updated Apr 12, 2018

Effect of "Kangaroo Mother Care" on Premature Infants Physiological Outcomes

An interventional study of Kangaroo care approach in Premature Neonate, sponsored by Jordan University of Science and Technology. Completed. Per ClinicalTrials.gov, last updated 2018-04-12.

Sponsored by Jordan University of Science and Technology · Not applicable, Interventional, and Supportive care

Phase
Not applicable
Study type
Interventional
Enrollment
35
Allocation
Randomized
Sex
All
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Study summary

This project aims at testing the effect of applying the KMC on the premature infants' physiological outcomes. The findings of this project are expected to contribute to the discipline of preterm infants' care by providing evidence of the benefits, barriers, and facilities of providing the KMC in our Jordanian NICUs.

Read the detailed description

Premature infants are often unable physiologically to adapt well to the stressful environment of the NICU. These neonates are commonly at risk for the development of short and long term outcomes ranging from mild developmental delay to severe disability. The Kangaroo mother care approach (KMC) is developed to minimize the effect of prematurity and the NICU environmental stressors on premature infants. This project aims at assessing the neonatal nurses' knowledge and attitudes of the application of the KMC approach in the neonatal intensive care unit (NICU), testing the effect of applying the KMC on the premature infants' physiological outcomes, and exploring the mothers' lived experiences of providing KMC for their premature infants. The findings of this project are expected to contribute to the discipline of preterm infants' care by providing evidence of the benefits, barriers, and facilities of providing the KMC in our Jordanian NICUs.

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Conditions studied

  • Premature Neonate

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03

In context

Premature Birth

2,554 studies on the registry are indexed under Premature Birth; 498 are open to participants now.

This study's enrollment of 35 is below the median of 84 across 1,689 interventional studies indexed under Premature Birth.

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Lead sponsor

Jordan University of Science and Technology is the lead sponsor of 88 studies on the registry; 7 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • all stable preterm or low birth weight infants (stable infants are those who are able to breath unassisted and have no major health problems (WHO, 2003)), weighing more than 1800gm, who are admitted to the NICUs at the time of study and whose mothers consent to participate and willing to practice the KMC with her infant

Exclusion criteria

Exclusion Criteria:

  • high risk preterm or low birth weight infants.
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Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Outcomes assessor)
Enrollment
35 participants (actual)

Study arms

  • Experimental
    kangaroo care approach

    the kangaroo care approach will be implemented for dyads who agree to participate

    Other: Kangaroo care approach

  • No intervention
    control group

    routine care will be implemented

Interventions

  • OtherKangaroo care approach

    skin to skin contact between stable preterm infants and their naked mother's chest

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What researchers measure

Primary outcomes

  1. Breastfeeding outcome

    Breastfeeding outcome will be measured for both groups by the numbers of preterm infants discharged on either exclusive or partial breastfeeding

    Time frame: 4-6 months

Secondary outcomes

  1. Body temperature

    Axillary body temperature will be measured using an electronic thermometer

    Time frame: 4-6 months

  2. Heart rate (beat per minute)

    Continuous electrocardiogram (ECG) data will be recorded from two surface chest electrodes

    Time frame: 4-6 months

  3. Respiratory activity (breath per minute)

    A non-invasive signal monitor connected to the infant cardio-respiratory monitor that captures ECG and respiratory data will be used

    Time frame: 4-6 months

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Study locations

No study locations are listed for this record.

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References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 12, 2018, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT02919540
Lead sponsor
Jordan University of Science and Technology
Responsible party
Sponsor
First posted
Sep 29, 2016
Start date
Sep 2016
Primary completion
Feb 24, 2018
Completion
Feb 24, 2018
Last update
Apr 12, 2018

Study contacts

khulood K. Shattnawi, PhD
principal investigator · Jordan University of Science and Technology

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Apr 2018. You cannot join it, but the record below documents what was studied.

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