Skip to main content
Clinical Trials/NCT06724328
NCT06724328
Completed
Not Applicable

Maternal Heartbeat Sounds and Therapeutic Touch

Dokuz Eylul University1 site in 1 country120 target enrollmentAugust 30, 2023

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Comfort
Sponsor
Dokuz Eylul University
Enrollment
120
Locations
1
Primary Endpoint
comfort
Status
Completed
Last Updated
11 months ago

Overview

Brief Summary

This randomized controlled study aims to evaluate the effects of maternal heartbeat sounds and gentle human touch (GHT), a form of therapeutic touch, on heart rate, comfort, and behavioral scores in neonates born between 32 and 40 weeks and admitted to the neonatal intensive care unit (NICU).

Detailed Description

This parallel, randomized controlled trial will be conducted in the Neonatal Intensive Care Unit of a regional hospital. The sample will consist of 120 neonates with gestational ages of 32 to ≤40 weeks and randomly assigned to four groups (maternal heart sound, therapeutic touch, maternal heart sound + therapeutic touch, and control group). The data of the study are the Newborn Information Form, the Anderson Behavioral Status Scoring System, and Newborn Comfort Behavior Scale. Demographic data will be compared between groups (maternal heartbeat sound group (Group 1), light human touch group (Group 2), combined maternal heartbeat sound and light human touch group (Group 3), and control group (Group 4)). Video recordings will be used to compare heart rate, behavioral status, and comfort scale scores obtained before, during, and after the interventions. The time it takes to fall asleep will also be evaluated. A t-test will be applied to evaluate the score differences between groups.

Registry
clinicaltrials.gov
Start Date
August 30, 2023
End Date
September 30, 2024
Last Updated
11 months ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Gülçin Özalp Gerçeker

Proffesor, Pediatric Nursing Department

Dokuz Eylul University

Eligibility Criteria

Inclusion Criteria

  • • Newborns between \>32 and ≤40 weeks gestational age.
  • Admission to neonatal intensive care unit (NICU) after birth.
  • Parental consent form obtained.

Exclusion Criteria

  • • Absence of neurological and cardiac problems.
  • No use of corticosteroids.
  • No use of muscle relaxants.
  • Not past the postnatal 10th day.
  • Not receiving non-invasive or invasive respiratory support.

Outcomes

Primary Outcomes

comfort

Time Frame: 0 minutes (pre-intervention), 5 minutes, 15 minutes, and 20 minutes (post-intervention)

It is a Likert-type scale consisting of seven parameters: alertness, calmness/agitation, respiratory response, crying, body movements, facial tension, and muscle tonus. As well as determining comfort, the COMFORTneo scale is a tool that includes numeric rating scales, which allow nurses to assess the pain and distress of the infant. The lowest score on the scale is 6, and the highest is 30. If the total score on the scale is between 14 and 30, the infant has pain or distress, is uncomfortable, and needs intervention to provide comfort. In addition, 4-6 points indicate moderate pain and distress, and 7-10 points indicate severe pain and distress

Secondary Outcomes

  • behavior(0 minutes (pre-intervention), 5 minutes, 15 minutes, and 20 minutes (post-intervention))

Study Sites (1)

Loading locations...

Similar Trials