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Clinical Trials/NCT02801331
NCT02801331
Completed
Not Applicable

A Randomized Controlled Study of Stochastic Vibrotactile Stimulation for Neonatal Abstinence Syndrome: Therapeutic Efficacy and Neurobehavioral Outcomes

Elisabeth B Salisbury1 site in 1 country208 target enrollmentMarch 9, 2017

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Neonatal Abstinence Syndrome
Sponsor
Elisabeth B Salisbury
Enrollment
208
Locations
1
Primary Endpoint
Number of Participants Administered Morphine Treatment
Status
Completed
Last Updated
10 months ago

Overview

Brief Summary

The purpose of this study is to examine the efficacy of a specially-constructed crib mattress that delivers gentle vibrations (stochastic vibrotactile stimulation) as a complementary, non-pharmacological intervention for treating drug withdrawal in newborns exposed to opioids in utero.

Detailed Description

This study will test the therapeutic efficacy of stochastic vibrotactile stimulation (SVS) for reducing withdrawal symptoms, pharmacological treatment and hospitalization, and for improving neurobehavioral developmental outcomes in opioid-exposed newborns. Candidates at-risk for NAS due opioid exposure in utero will be identified to investigators by medical caregiver and/or prescreened using HIPAA Waiver for recruitment (maternal-prenatal; infant-postnatal). Infants will be randomized into either SVS (complementary to standard of care) or Treatment as Usual (TAU), restricted by equipment (mattress) availability. Infants will be enrolled and assigned to a condition within 48 hours post birth and participate throughout hospitalization. Infants assigned SVS will receive daily intervention of continuous intervals of SVS throughout hospitalization using a specially constructed crib mattress that delivers gentle vibrations at preset intervals. Specific Aim 1. Determine the efficacy of SVS as a non-pharmacological therapy complementary to standard of care for reducing severity and duration of opioid withdrawal in newborns compared to TAU alone. Quantify clinical variables: NAS severity, treatment days, days in hospital, velocity of weight gain, cumulative morphine dose. Specific Aim 2. Compare neurobehavioral outcomes in fetal drug-exposed infants between infants who received SVS and those who received TAU. Longitudinal outcomes assessment at 6-months and 1 year to test whether early intervention with SVS compared to standard care improves physical, social, emotional and cognitive development.

Registry
clinicaltrials.gov
Start Date
March 9, 2017
End Date
June 6, 2021
Last Updated
10 months ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Elisabeth B Salisbury
Responsible Party
Sponsor Investigator
Principal Investigator

Elisabeth B Salisbury

Visiting Associate Professor

University of Pittsburgh

Eligibility Criteria

Inclusion Criteria

  • Eligible subjects are infants currently in the NICU or Newborn Nursery at University of Massachusetts Memorial Hospital or at Magee Women's Hospital of UPMC and:
  • Full-term infants (≥37 wks gestational age)
  • Newborns at risk for NAS due to opioid-exposure in utero
  • At-risk infants will be infants who present with confirmed meconium and/or urine toxicology report and/or documented medical record for opioids (e.g., methadone, buprenorphine/subutex, oxycodone, heroin); may also have prenatal exposure to benzodiazepines, barbiturates, amphetamines, cannabinoids, alcohol, nicotine and/or caffeine.

Exclusion Criteria

  • Eligible infants meeting the inclusion criteria above will be excluded from participation in the study if he/she:
  • Born less than \<37weeks.
  • Has a clinically significant congenital abnormality
  • Has a clinically significant fetal anomaly
  • Has hydrocephalus or intraventricular hemorrhage \>grade 2
  • Has a seizure disorder not related to drug withdrawal
  • Has a clinically significant cardiac shunt
  • Has anemia (hemoglobin\<8g/dL)
  • Requires mechanical respiratory support
  • Has MRSA or infection at time of the study

Outcomes

Primary Outcomes

Number of Participants Administered Morphine Treatment

Time Frame: Participants will be monitored for the duration of their newborn nursery stay, which is an expected mean of 7 days

Number of infants treated with morphine (first line pharmacotherapy at both sites). Number of infants who received pharmacotherapy (met clinical criteria to treat), index of NAS severity (per Finnegan scores).

Cumulative Pharmacological Treatment- Morphine Dose

Time Frame: Participants will be monitored for the duration of their hospitalization, which is an expected mean of 21 days

Normalized cumulative morphine dose for infants who completed treatment at respective hospital site (mg/kg).

Hospitalization Length of Stay for Untreated Infants

Time Frame: Day of life untreated infants discharged home, which is an expected mean of 21 days.

Day of life discharged home for untreated infants (infants whose Finnegan scores did not meet criteria to treat) who completed hospitalization at study site. Duration of infant hospitalization-Days

Velocity of Weight Gain

Time Frame: Participants will be monitored for the duration of their hospitalization, which is an expected mean of 21 days

Weight loss precedes weight gain in newborns. Days to weight nadir, defined as the lowest weight following birthweight. Velocity of weight gain was measured as days to return to birthweight, i.e., the day on which weight reached or surpassed birthweight following initial weight loss from birth.

Hospitalization Length of Stay

Time Frame: Day of life infants discharged home, which is an expected mean of 21 days.

Day of life discharged home for untreated and treated infants who completed hospitalization at study site. Duration of infant hospitalization-Days

Neurobehavioral Outcomes Assessment

Time Frame: 6 month and 12 months of life

Scores for Cognitive Domain Bayley Scales of Infant and Toddler Development Third Edition. The standardized scores have a mean of 100 and standard deviation (SD) of 15. Scores below 1 SD (= or less than 84) is considered below normal. Scores above 1 SD (\>115) represent higher than normal functioning.

Hospitalization Length of Stay for Treated Infants

Time Frame: Day of life treated infants discharged home, which is an expected mean of 21 days.

Day of life discharged home for treated infants (infants whose Finnegan scores met criteria to treat) who completed hospitalization at study site. Duration of infant hospitalization-Days

Length of Pharmacological Treatment-Duration

Time Frame: Participants will be monitored for the duration of their hospitalization, which is an expected mean of 21 days

For infants who received pharmacotherapy, total days of morphine treatment.

Trajectory of Symptom Severity Among Treated Infants

Time Frame: Day of life infant started morphine treatment

Days to start morphine treatment based on Finnegan severity scores among infants who met clinical criteria to treat

Study Sites (1)

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