Study Results
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View full resultsBasic Information
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COMPLETED
NA
100 participants
INTERVENTIONAL
2012-04-30
2013-06-30
Brief Summary
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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.
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Detailed Description
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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.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
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Pacifier-Activated-Lullaby system (PAL)
Pacifier-Activated-Lullaby system (PAL) group.
Pacifier-Activated-Lullaby system (PAL).
Pacifier-Activated-Lullaby system (PAL).
No PAL group
No PAL. Standard of care procedures.
No interventions assigned to this group
Interventions
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Pacifier-Activated-Lullaby system (PAL).
Pacifier-Activated-Lullaby system (PAL).
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* infants determined to be unsafe to feed orally by the medical team or the feeding/speech specialists at Vanderbilt.
34 Weeks
36 Weeks
ALL
No
Sponsors
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Vanderbilt Kennedy Center
OTHER
National Center for Research Resources (NCRR)
NIH
Vanderbilt University Medical Center
OTHER
Responsible Party
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Principal Investigators
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Olena D Chorna, MM, MT-BC
Role: PRINCIPAL_INVESTIGATOR
Vanderbilt University Medical Center
Locations
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Monroe Carell Jr. Children's Hospital at Vanderbilt
Nashville, Tennessee, United States
Countries
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Other Identifiers
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VKC 4-30-100-9622
Identifier Type: -
Identifier Source: org_study_id
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