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A Clinical Trial of A Pacifier-Activated Music Player

Primary Purpose

Prematurity

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Pacifier-Activated-Lullaby system (PAL).
Sponsored by
Vanderbilt University Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Prematurity focused on measuring Neonatal Intensive Care Unit (NICU), Music therapy, Premature infant, Oral feeds, Non-Nutritive Sucking, Suck rate, Suck efficiency, Contingent music, Mother's voice

Eligibility Criteria

34 Weeks - 36 Weeks (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • All infants at 34 0/7 to 35 6/7 weeks post-conceptional age cared for in the Vanderbilt NICU who are receiving more than 50 % of their nutrition as enteral feeds, and are in individual rooms or in the room with their sibling.

Exclusion Criteria:

  • infants on ventilators or Continuous Positive Airway Pressure (CPAP),
  • infants determined to be unsafe to feed orally by the medical team or the feeding/speech specialists at Vanderbilt.

Sites / Locations

  • Monroe Carell Jr. Children's Hospital at Vanderbilt

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Pacifier-Activated-Lullaby system (PAL)

No PAL group

Arm Description

Pacifier-Activated-Lullaby system (PAL) group.

No PAL. Standard of care procedures.

Outcomes

Primary Outcome Measures

Suck Rate and Efficiency: Change From Pre-test (Day 0) to Post-test (Day 5)
Feeding rate when nippling was calculated by dividing the number of cc of nippled nutrition by time for consumption. This data was recorded at two time points: pre and post intervention

Secondary Outcome Measures

Discharge Weight
Description: Growth measures.
Change From Pre-test(Day 0)in Salivary Cortisol Levels to Post-test (Day 5)
Description: Stress: Salivary cortisol levels at baseline and after 1 week of PAL in the intervention group.
Hospital Length of Stay
Description: Data on hospital stay was recorded from the chart. The participants were be followed for the duration of the hospital stay from the time of consent for participation to the time discharge from the NICU is documented.
Number of Days to Full Oral Feeds
Aim: Quantify the effect of the PAL intervention on efficiency of sucking and time to reaching full oral feeds in comparison to controls. Data on the number of days from Day 0 of the study to the date of first documented full oral feed, up to 70 days (or date of death from any cause) were be recorded from the chart.

Full Information

First Posted
May 9, 2012
Last Updated
April 4, 2018
Sponsor
Vanderbilt University Medical Center
Collaborators
Vanderbilt Kennedy Center, National Center for Research Resources (NCRR)
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1. Study Identification

Unique Protocol Identification Number
NCT01600586
Brief Title
A Clinical Trial of A Pacifier-Activated Music Player
Official Title
A Pacifier-Activated Music Player With Mother's Voice Improves Oral Feeding in Preterm Infants
Study Type
Interventional

2. Study Status

Record Verification Date
April 2018
Overall Recruitment Status
Completed
Study Start Date
April 2012 (undefined)
Primary Completion Date
June 2013 (Actual)
Study Completion Date
June 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Vanderbilt University Medical Center
Collaborators
Vanderbilt Kennedy Center, National Center for Research Resources (NCRR)

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Neonatal intensive care unit infants are at high risk for oromotor difficulties including poor coordination of sucking swallowing and breathing. These feeding difficulties often result in prolonged hospitalization, with increased physiologic stressors and poor growth. In preliminary studies, Pacifier Activated Lullaby (PAL) use showed potential increased oromotor skills and decreased length of hospitalization. The investigators propose to test the hypothesis that a week-long PAL intervention can improve feeding skills and decrease stress compared to standard of care parental interactions in infants in the late preterm period. The investigators also hypothesize that these improvements will result in shorter hospital stays and increased growth in the intervention group. Our study design is a prospective randomized controlled trial design of 94 infants (Post-conceptional ages 34-36 weeks). The 47 intervention-group infant/mother dads will receive a book library with one lullaby book and record her voice to the PAL, which the music therapist will then administer in 15-minute sessions for 5 consecutive days. The 47 participants in the control group will receive the same library but no recording will be made or PAL used. Outcomes measured will include time to full oral feeds, suck rate and efficiency, salivary cortisol levels before and after intervention, daily growth parameters and nutritional data, and hospital length of stay.
Detailed Description
Objectives: We conducted a randomized trial to test the hypothesis that the mother's voice played through a pacifier-activated music (PAM) player during nonnutritive sucking would improve the development of sucking ability and promote more effective oral feeding in preterm infants. Methods: Preterm infants between 34 0/7 and 35 6/7 weeks postmenstrual age, including those with brain injury, who were taking at least half their feedings enterally and less than half orally, were randomly assigned to receive 5 daily 15-minute sessions of either PAM with mother's recorded voice or no PAM, along with routine nonnutritive sucking and maternal care in both groups. Assignment was masked to the clinical team.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prematurity
Keywords
Neonatal Intensive Care Unit (NICU), Music therapy, Premature infant, Oral feeds, Non-Nutritive Sucking, Suck rate, Suck efficiency, Contingent music, Mother's voice

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
100 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Pacifier-Activated-Lullaby system (PAL)
Arm Type
Experimental
Arm Description
Pacifier-Activated-Lullaby system (PAL) group.
Arm Title
No PAL group
Arm Type
No Intervention
Arm Description
No PAL. Standard of care procedures.
Intervention Type
Device
Intervention Name(s)
Pacifier-Activated-Lullaby system (PAL).
Intervention Description
Pacifier-Activated-Lullaby system (PAL).
Primary Outcome Measure Information:
Title
Suck Rate and Efficiency: Change From Pre-test (Day 0) to Post-test (Day 5)
Description
Feeding rate when nippling was calculated by dividing the number of cc of nippled nutrition by time for consumption. This data was recorded at two time points: pre and post intervention
Time Frame
Day 0, and Day 5
Secondary Outcome Measure Information:
Title
Discharge Weight
Description
Description: Growth measures.
Time Frame
day of hospital discharge (approximately 5-7 weeks)
Title
Change From Pre-test(Day 0)in Salivary Cortisol Levels to Post-test (Day 5)
Description
Description: Stress: Salivary cortisol levels at baseline and after 1 week of PAL in the intervention group.
Time Frame
Day 0, and Day 5
Title
Hospital Length of Stay
Description
Description: Data on hospital stay was recorded from the chart. The participants were be followed for the duration of the hospital stay from the time of consent for participation to the time discharge from the NICU is documented.
Time Frame
days from consent to discharge
Title
Number of Days to Full Oral Feeds
Description
Aim: Quantify the effect of the PAL intervention on efficiency of sucking and time to reaching full oral feeds in comparison to controls. Data on the number of days from Day 0 of the study to the date of first documented full oral feed, up to 70 days (or date of death from any cause) were be recorded from the chart.
Time Frame
Day 0 of the study to the date of first documented full oral feed (up to 70 days)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
34 Weeks
Maximum Age & Unit of Time
36 Weeks
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: All infants at 34 0/7 to 35 6/7 weeks post-conceptional age cared for in the Vanderbilt NICU who are receiving more than 50 % of their nutrition as enteral feeds, and are in individual rooms or in the room with their sibling. Exclusion Criteria: infants on ventilators or Continuous Positive Airway Pressure (CPAP), infants determined to be unsafe to feed orally by the medical team or the feeding/speech specialists at Vanderbilt.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Olena D Chorna, MM, MT-BC
Organizational Affiliation
Vanderbilt University Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Monroe Carell Jr. Children's Hospital at Vanderbilt
City
Nashville
State/Province
Tennessee
ZIP/Postal Code
37232
Country
United States

12. IPD Sharing Statement

Learn more about this trial

A Clinical Trial of A Pacifier-Activated Music Player

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