LongSTEP: Longitudinal Study of Music Therapy's Effectiveness for Premature Infants and Their Caregivers

Sponsor
NORCE Norwegian Research Centre AS (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT03564184
Collaborator
Haukeland University Hospital (Other), University Hospital, Akershus (Other), Oslo University Hospital (Other), Meir Medical Center (Other), Clinica de La Mujer (Other), University of Haifa (Other), University of Gdansk (Other), King's College London (Other), Universidad de Ciencias Empresariales y Sociales (Other), Szpital Miejski w Rudzie Śląskiej (Other), SONO - Centro de Musicoterapia (Other), Hospital Materno Infantil Ramón Sardá (Other), Hospital Fernandez (Other)
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Study Details

Study Description

Brief Summary

Background: Preterm birth has major medical, psychological and socio-economic consequences worldwide. A recent systematic review suggests positive effects of music therapy (MT) on physiological measures of preterm infants and maternal anxiety, but methodologically rigorous studies including long-term follow-up of infant and parental outcomes are missing. Drawing upon caregivers' inherent resources, this study emphasizes caregiver involvement in MT to promote attuned, developmentally-appropriate musical interactions that may be of mutual benefit to infant and parent. This study will determine whether MT, as delivered by a qualified music therapist during neonatal intensive care unit (NICU) hospitalization and/or in home/municipal settings following discharge, is superior to standard care in improving bonding between primary caregivers and preterm infants, parent well-being and infant development.

Methods: Design: International multi-center, assessor-blind, 2x2 factorial, pragmatic randomized controlled trial. A feasibility study has been completed; ethical approval for the main trial is pending. Participants: 250 preterm infants and their parents. Intervention: MT focusing on singing specifically tailored to infant responses, will be delivered during NICU and/or during a post-discharge 6-month period. Primary outcome: Changes in mother-infant bonding until 6 months corrected age (CA), as measured by the Postpartum Bonding Questionnaire. Secondary outcomes: Mother-infant bonding at discharge and over 12 months CA; child development over 24 months; and parental depression, anxiety, and stress, and infant re-hospitalization, all over 12 months.

Discussion: This study fills a gap by measuring the long-term impact of MT for preterm infants/caregivers, and of MT beyond the hospital context. Outcomes related to highly involving parents in MT will directly inform the development of clinical practice in Scandinavia and other contexts with similar social welfare practices. By incorporating family-centered care, continuity of care, user involvement, and cultural relevance, this study can potentially contribute to improved quality of care for premature infants and their parents worldwide.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: MT during NICU
  • Behavioral: MT after NICU
  • Other: Standard care
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
213 participants
Allocation:
Randomized
Intervention Model:
Factorial Assignment
Intervention Model Description:
2x2 factorial, multinational, single-blind trial2x2 factorial, multinational, single-blind trial
Masking:
Single (Outcomes Assessor)
Masking Description:
Data collectors (for self-reports) and assessors (for observational measures) will be trained in assessment procedures and blinded to participant allocation. This will be ensured by using assessors from a different ward and by asking participants not to reveal their treatment assignments. Success of blinding will be verified.
Primary Purpose:
Treatment
Official Title:
Longitudinal Study of Music Therapy's Effectiveness for Premature Infants and Their Caregivers: International Randomized Trial
Actual Study Start Date :
Aug 25, 2018
Actual Primary Completion Date :
Dec 31, 2020
Anticipated Study Completion Date :
Jun 30, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: MT during and after NICU

Consists of music therapy during NICU hospitalization, and music therapy after discharge from initial NICU hospitalization, along with standard care.

Behavioral: MT during NICU
Music therapy (MT) by trained music therapist, 3 times/week for 30-40 minutes/session during NICU hospitalization. Involves primary caregiver and infant in musical communication matched to infant post-menstrual age, family/cultural preferences, and infant readiness for stimulation. Music therapist assesses infant´s needs and behavior state, supports caregiver in using basic touch (e.g., hand lightly and statically on infant´s chest or back to perceive breathing pattern) and caregiver´s hummed/sung voice matched to infant behavioral responses, to promote infant state regulation and bonding. Music includes input from music therapist as needed, and multimodal aspects such as gentle dynamic touch when infant demonstrates readiness. MT may occur while infant is held in a static manner by caregiver or is resting in his/her isolette or basinet. MT may occur during skin-to-skin care, if such care is part of standard care.

Behavioral: MT after NICU
Music therapy offered by trained music therapist, 7 times for approximately 45 minutes/session across first 6 months following discharge from initial NICU hospitalization. Sessions include infant and caregiver, and siblings, if desired, and occur at home or in municipal settings. MT after NICU consists of a consult-to-parent model with each session including a brief verbal check-in regarding infant´s progress, musical interactions with music therapist modelling musical engagement, discussion of current challenges and strategies for using musical interactions to address needs in areas such as infant self-regulation, parent/infant interaction, and challenges with bonding. Caregivers will demonstrate techniques discussed during session, and form a brief plan for use of musical interaction in the interim before next session. Sessions will be adapted to infant developmental level and ongoing needs.

Other: Standard care
Includes necessary medical care and standard supportive interventions offered as part of care during hospitalization, and standard follow-up procedures post-hospitalization.

Experimental: MT during NICU

Consists of music therapy during NICU hospitalization, along with standard care.

Behavioral: MT during NICU
Music therapy (MT) by trained music therapist, 3 times/week for 30-40 minutes/session during NICU hospitalization. Involves primary caregiver and infant in musical communication matched to infant post-menstrual age, family/cultural preferences, and infant readiness for stimulation. Music therapist assesses infant´s needs and behavior state, supports caregiver in using basic touch (e.g., hand lightly and statically on infant´s chest or back to perceive breathing pattern) and caregiver´s hummed/sung voice matched to infant behavioral responses, to promote infant state regulation and bonding. Music includes input from music therapist as needed, and multimodal aspects such as gentle dynamic touch when infant demonstrates readiness. MT may occur while infant is held in a static manner by caregiver or is resting in his/her isolette or basinet. MT may occur during skin-to-skin care, if such care is part of standard care.

Other: Standard care
Includes necessary medical care and standard supportive interventions offered as part of care during hospitalization, and standard follow-up procedures post-hospitalization.

Experimental: MT after NICU

Consists of music therapy after discharge from initial NICU hospitalization, along with standard care.

Behavioral: MT after NICU
Music therapy offered by trained music therapist, 7 times for approximately 45 minutes/session across first 6 months following discharge from initial NICU hospitalization. Sessions include infant and caregiver, and siblings, if desired, and occur at home or in municipal settings. MT after NICU consists of a consult-to-parent model with each session including a brief verbal check-in regarding infant´s progress, musical interactions with music therapist modelling musical engagement, discussion of current challenges and strategies for using musical interactions to address needs in areas such as infant self-regulation, parent/infant interaction, and challenges with bonding. Caregivers will demonstrate techniques discussed during session, and form a brief plan for use of musical interaction in the interim before next session. Sessions will be adapted to infant developmental level and ongoing needs.

Other: Standard care
Includes necessary medical care and standard supportive interventions offered as part of care during hospitalization, and standard follow-up procedures post-hospitalization.

Experimental: No MT

Consists of standard care.

Other: Standard care
Includes necessary medical care and standard supportive interventions offered as part of care during hospitalization, and standard follow-up procedures post-hospitalization.

Outcome Measures

Primary Outcome Measures

  1. Bonding between primary caregiver and infant [6 months]

    Total score of the Postpartum Bonding Questionnaire (PBQ), a parent-rated screening instrument for disorders of the early mother-infant relationship consisting of 25 statements on a six-point Likert scale (each 0-5; sum score ranging from 0 to 125; high = problematic).

Secondary Outcome Measures

  1. Bonding between primary caregiver and infant [12 months]

    Total score of the Postpartum Bonding Questionnaire (PBQ), a parent-rated screening instrument for disorders of the early mother-infant relationship consisting of 25 statements on a six-point Likert scale (each 0-5; sum score ranging from 0 to 125; high = problematic).

  2. Child development [24 months]

    Bayley Scales of Infant and Toddler Development, 3rd edition (Bayley-III), standardized with a population mean of 100 (SD 15), with higher scores indicating better development

  3. Infant development [12 months]

    Ages and Stages Questionnaire, 3rd edition (ASQ-3), an age-specific parent-reported screening questionnaire consisting of 30 items, total sum score ranging from 0 to 300, with higher scores indicating better development.

  4. Infant socio-emotional development [12 months]

    Ages and Stages Questionnaire Social-Emotional (ASQ:SE), a parent-completed questionnaire with 19 or 22 Likert-scaled items (each 0-5-10), plus additional items for whether an item is of concern to the parent (each 0-5), resulting in a score ranging from 0-285 or 0-300, at 6 and 12 months respectively. Lower scores indicate better socio-emotional development.

  5. Re-hospitalization [12 months]

    Re-hospitalization excluding outpatient visits, based on electronic health records. This will be calculated as the time from initial discharge until first re-hospitalization.

  6. Maternal depression [12 months]

    Edinburgh Postnatal Depression Scale (EPDS), a 10-item validated self-report instrument assessing mothers' postpartum depressive symptoms, excluding somatic symptoms of depression that are common in new mothers (such as loss of energy, feeling tired, changes in appetite and sexual drive). Sum scores can range from 0 to 30, with high scores indicating more depressive symptoms.

  7. Parental anxiety [12 months]

    Generalized Anxiety Disorder Assessment (GAD-7), a self-report 7-item questionnaire serving as a screening tool and severity measure for generalized anxiety disorder. Sum scores can range from 0 to 21, with higher scores indicating higher anxiety.

  8. Parental stress [12 months]

    Parental Stress Scale (PSS), a self-report 18-item questionnaire that assesses stress associated with parenting. Sum scores can range from 18 to 90, with higher scores indicating higher stress.

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria (infants):
  • born below 35 weeks gestational age

  • determined by medical staff to have achieved sufficient medical stability to start MT

  • likely to be hospitalized longer than 2 weeks from time of recruitment

Inclusion Criteria (parents):
  • willing to engage in at least 2 of 3 MT sessions per week during NICU and/or in 5 of 7 MT post-discharge sessions, if randomized to receive MT

  • live with reasonable commuting distance from the treating NICU

  • sufficient understanding of the respective national language(s) to answer questionnaires and participate in MT

Exclusion Criteria (parents):
  • documented mental illness or cognitive impairment that prevents them from being able to complete the study intervention or outcome assessments

Contacts and Locations

Locations

Site City State Country Postal Code
1 Hospital Materno Infantil Ramón Sardá Buenos Aires Caba Argentina 1246
2 Sanatorio Mater Dei Buenos Aires Caba Argentina C1425DND
3 Hospital Fernandez Buenos Aires Argentina
4 Clinica de la Mujer Bogotá Colombia
5 Fundación Santa Fe de Bogotá Bogotá Colombia
6 Meir Medical Center Kfar Saba Israel 4428164
7 Haukeland University Hospital, Barne-og ungdomsklinikken Bergen Hordaland Norway 5006
8 Akershus University Hospital Oslo Lørenskog Norway 1478
9 Oslo University Hospital, Rikshospitalet Oslo Norway 0424
10 Szpital Miejski w Rudzie Śląskiej Ruda Śląska Poland 41-703

Sponsors and Collaborators

  • NORCE Norwegian Research Centre AS
  • Haukeland University Hospital
  • University Hospital, Akershus
  • Oslo University Hospital
  • Meir Medical Center
  • Clinica de La Mujer
  • University of Haifa
  • University of Gdansk
  • King's College London
  • Universidad de Ciencias Empresariales y Sociales
  • Szpital Miejski w Rudzie Śląskiej
  • SONO - Centro de Musicoterapia
  • Hospital Materno Infantil Ramón Sardá
  • Hospital Fernandez

Investigators

  • Study Chair: Christian Gold, PhD, NORCE Norwegian Research Centre
  • Principal Investigator: Claire Ghetti, PhD, Grieg Academy, University of Bergen

Study Documents (Full-Text)

None provided.

More Information

Additional Information:

Publications

Responsible Party:
Christian Gold, Research Professor, NORCE Norwegian Research Centre AS
ClinicalTrials.gov Identifier:
NCT03564184
Other Study ID Numbers:
  • RCN 273534
First Posted:
Jun 20, 2018
Last Update Posted:
Apr 1, 2021
Last Verified:
Mar 1, 2021
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Christian Gold, Research Professor, NORCE Norwegian Research Centre AS
Additional relevant MeSH terms:

Study Results

No Results Posted as of Apr 1, 2021