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Early Parenting Intervention: Bio-behavioral Outcomes in Infants With Neurodevelopmental Disabilities (EPI-BOND)

Primary Purpose

Epigenomics, Developmental Disability, Early Intervention

Status
Completed
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
Video-Feedback Intervention
Phone-Call Intervention
Sponsored by
IRCCS Eugenio Medea
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Epigenomics focused on measuring DNA methylation, Epigenetic regulation, Video-feedback intervention, Developmental disability, Cerebral palsy, Genetic syndromes, Parent-infant interaction, Early intervention, Neuroendocrine regulation

Eligibility Criteria

3 Months - 18 Months (Child)All SexesDoes not accept healthy volunteers

ELIGIBILITY CRITERIA FOR INFANTS

Inclusion Criteria:

  • Infants with equivalent age range 3-to-18-months
  • Mild to moderate psychomotor delay

Exclusion Criteria:

  • Presence of severe sensorial (auditory, visual) deficits
  • Genetic syndrome with known functional implications for the epigenetic regulation of target genes

ELIGIBILITY CRITERIA FOR MOTHERS

Inclusion Criteria:

  • Mastery of Italian language
  • Age > 18 years
  • Living with the father of the infant

Exclusion Criteria:

  • Documented mental disorder
  • Documented disability

Sites / Locations

  • IRCCS E. Medea
  • Università degli Studi di Brescia
  • Fondazione Istituto Neurologico Casimiro Mondino

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Sham Comparator

Arm Label

Video-Feedback Group (VFG)

Phone-Call Group (PCG)

Arm Description

Dyads of mothers and their infant with developmental disability who are exposed to the video-feedback intervention focused on different domains of mother-infant quality of interaction (number of sessions: 6).

Dyads of mothers and their infant with developmental disability who are not exposed to the video-feedback intervention, instead they receive phone calls focused on obtaining descriptions of different domains of infant behavioral development (number of sessions: 6)

Outcomes

Primary Outcome Measures

Change in maternal sensitivity
Coded micro-analitically from videotapes of mother-infant interactions.
Change in infant behavioral regulation
Coded micro-analitically from videotapes of mother-infant interactions.

Secondary Outcome Measures

Change in hormones salivary concentrations
Salivary cortisol and oxytocin obtained from infants by trained collaborators.
Change in DNA methylation status
The methylation status of target genes (e.g., NR3C1, SLC6A4, BDNF, OXTR) will be assessed from salivary samples obtained from infants.

Full Information

First Posted
February 19, 2019
Last Updated
October 17, 2023
Sponsor
IRCCS Eugenio Medea
Collaborators
Fondazione Istituto Neurologico Casimiro Mondino, Università degli Studi di Brescia
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1. Study Identification

Unique Protocol Identification Number
NCT03853564
Brief Title
Early Parenting Intervention: Bio-behavioral Outcomes in Infants With Neurodevelopmental Disabilities
Acronym
EPI-BOND
Official Title
Clinical Trial of an Early Parenting Empowerment Intervention to Promote Socioemotional Development in Infants With Developmental Disabilities: Parent and Infant Behavioral, Neuroendocrine and Epigenetics Outcomes
Study Type
Interventional

2. Study Status

Record Verification Date
October 2023
Overall Recruitment Status
Completed
Study Start Date
September 1, 2019 (Actual)
Primary Completion Date
February 5, 2023 (Actual)
Study Completion Date
April 5, 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
IRCCS Eugenio Medea
Collaborators
Fondazione Istituto Neurologico Casimiro Mondino, Università degli Studi di Brescia

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Infants with developmental disabilities present a high risk of behavioral and socio-emotional problems. Their parents are themselves at risk of developing emotional and affective disorders which can impact the quality of the interaction with the infant. Early parenting empowerment focused on parent-infant interaction are beneficial in supporting infants development and parental adjustment. By using a multi-layer approach to outcomes assessment (i.e., behavioral, neuroendocrine and epigenetic outcomes), the present longitudinal, multi-center, change-promoting clinical trial is aimed at assessing the effectiveness of an early parenting empowerment intervention based on video-feedback technique to support maternal responsiveness and the socio-emotional development of infants with developmental disabilities.
Detailed Description
RATIONALE: Infants with developmental disabilities (e.g., cerebral palsy and genetic syndrome) present a high risk of behavioral and socio-emotional problems. Their parents are themselves at risk of developing emotional and affective disorders which can impact the quality of the interaction with the infant. Typical development research is highlighting the potentials of biological markers of less-than-optimal mother-infant interaction, such as altered neuroendocrine regulation (i.e., cortisol and oxytocin). Increased infants' salivary cortisol reactivity has been found in response to experimental suspension of maternal responsiveness (Still-Face paradigm, SFP). On the other hand, oxytocin administration to mothers increases responsiveness to infants socio-emotional signals and oxytocin has also been associated with socioemotional stress regulation in humans. Interestingly, previous research suggests that the epigenetic regulation of specific genes (i.e., SLC6A4, NR3C1, BDNF, OXTR) transcription might be affected by alterations of maternal caregiving behavior. Nonetheless, to the best of our knowledge, to date there is no investigation of the epigenetic vestiges of the effects of an early parenting intervention (i.e., video-feedback) on the behavioral outcomes of infants with developmental disabilities. SPECIFIC AIM 1: To assess the effectiveness of the video-feedback intervention to enhance the socio-emotional behavior of infants with developmental disabilities. EXPERIMENTAL DESIGN AIM 1: The present research project will include two groups (Video-Feedback Group, VFG; Phone-Call Group, PCG) and four phases: T0, baseline assessment; T1, post-intervention assessment ; T2, follow-up#1 (3 months after the intervention); T3, follow-up#2 (6 months after the intervention). All infants and their mothers will be enrolled at three Child Neuropsychiatric Units in Lombardia Region (OU1, Scientific Institute IRCCS E. Medea; OU2, Fondazione Istituto Neurologico Casimiro Mondino, Pavia, Italy; OU3, Università degli Studi, Brescia, Italy). At each phase, mother-infant interactions will be videotaped during SFP. The VFG dyads will participate to a 6-session videofeedback intervention The aim of the video-feedback intervention is to support maternal sensitivity to the infants' behaviors focusing on different aspects of mother-infant interactions. PCG mothers will be contacted by telephone weekly for 6 weeks, and will be asked for information on their infants' development. No advice about sensitive parenting will be given to the control PCG mothers during these conversations. In each of the three Units, the intervention will be conducted by psychologists/developmental neuropsychiatrists trained on the video-feedback intervention. Infant behavior regulation will be observationally assessed at each of the four phases of the research project. SPECIFIC AIM 2: To examine the effects of the intervention on maternal responsiveness. EXPERIMENTAL DESIGN AIM 2: Paralleling infants' behavioral assessment, maternal responsiveness will be assessed at each project phase by means of video-tapes. Additionally, maternal reports of emotional and affective states, including depressive and anxious symptoms and stress perception in taking care of the infant, will be obtained and controlled for. The rate of change over the phases of the project in maternal self-reported emotional states, feelings of attachment and coded sensitivity will concur in defining the efficacy of the intervention in the VFG subjects against the PCG counterparts. SPECIFIC AIM 3: To investigate the immediate and follow-up pre/post intervention variations in the neuroendocrine functioning (i.e., salivary cortisol and oxytocin) and in the DNA methylation of specific genes associated with infants' behavioral regulation such as: NR3C1, BDNF, SLC6A4, OXTR. EXPERIMENTAL DESIGN AIM 3: Salivary samples will be collected from the infant at each phase before and after the SFP interaction. For what pertains neuroendocrine markers (i.e., salivary cortisol and oxytocin) saliva will be collected from the infants (and mothers) using an oral cotton swab and it will be collected in eppendorf, centrifuged and conserved according to kit producer guidelines. Samples will be obtained before (1 sample) and after (3 samples: +10, +20, and +30 minutes) the SFP procedure. Due to circadian rhythm of the neuroendocrine systems, all the interactions will occur in the morning, between 9.00 and 12.00 AM. For what pertains the epigenetic profiling, saliva will be collected once per phase. DNA methylation will be assessed at the different CpG sites within the promoter regions of specific target genes (NR3C1, SLC6A4, BDNF, OXTR) previously associated with infants' behavioral development. The rate of change in neuroendocrine concentrations of cortisol and oxytocin as well as the alterations in global and site-specific DNA methylation of the selected genes will be used as independent biomarkers of the effects of the video-feedback intervention. SIGNIFICANCE AND INNOVATION: First, the study has the potential to bring new evidence in the clinical practices promoting an early intervention for mothers of infants with developmental disabilities. Second, the multi-center nature of this clinical trial will provide a common early intervention program in the Italian context, with potential indirect implication for healthcare costs optimization. Indeed, it has been shown that interventions starting earlier in childhood may be more effective and efficient than those provided in a later period of life. Consistently, the project will be conducted during the first year of life of infants with the potential to permanently alter infants' development trajectories and to yield a significant economic return for the healthcare system. Finally, examining the epigenetic variations related to early parenting intervention the project introduces an innovative approach to early intervention research for families of infants with developmental disabilities.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Epigenomics, Developmental Disability, Early Intervention, Parent-Child Relations
Keywords
DNA methylation, Epigenetic regulation, Video-feedback intervention, Developmental disability, Cerebral palsy, Genetic syndromes, Parent-infant interaction, Early intervention, Neuroendocrine regulation

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
45 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Video-Feedback Group (VFG)
Arm Type
Experimental
Arm Description
Dyads of mothers and their infant with developmental disability who are exposed to the video-feedback intervention focused on different domains of mother-infant quality of interaction (number of sessions: 6).
Arm Title
Phone-Call Group (PCG)
Arm Type
Sham Comparator
Arm Description
Dyads of mothers and their infant with developmental disability who are not exposed to the video-feedback intervention, instead they receive phone calls focused on obtaining descriptions of different domains of infant behavioral development (number of sessions: 6)
Intervention Type
Behavioral
Intervention Name(s)
Video-Feedback Intervention
Intervention Description
Mothers and infants of the VFG arm will participate to a 6-session video-feedback intervention structured as follows: 4 sessions of video-review discussions with a trained clinician + 2 sessions of integrative intervention aimed at translating into practical caregiving the insights developed during the video-review discussions.
Intervention Type
Other
Intervention Name(s)
Phone-Call Intervention
Intervention Description
Mothers of the PCG arm will participate in 6-session of telephone call during which a trained collaborator will ask details on different domains of infants behavioral development.
Primary Outcome Measure Information:
Title
Change in maternal sensitivity
Description
Coded micro-analitically from videotapes of mother-infant interactions.
Time Frame
Through study completion: at intervention start (Baseline, T0), 2 months after intervention start (post-intervention, T1), 3 months after intervention end (follow-up, T2), and 6 months after intervention end (follow-up, T3)
Title
Change in infant behavioral regulation
Description
Coded micro-analitically from videotapes of mother-infant interactions.
Time Frame
Through study completion: at intervention start (Baseline, T0), 2 months after intervention start (post-intervention, T1), 3 months after intervention end (follow-up, T2), and 6 months after intervention end (follow-up, T3)
Secondary Outcome Measure Information:
Title
Change in hormones salivary concentrations
Description
Salivary cortisol and oxytocin obtained from infants by trained collaborators.
Time Frame
Through study completion: at intervention start (Baseline, T0), 2 months after intervention start (post-intervention, T1), 3 months after intervention end (follow-up, T2), and 6 months after intervention end (follow-up, T3)
Title
Change in DNA methylation status
Description
The methylation status of target genes (e.g., NR3C1, SLC6A4, BDNF, OXTR) will be assessed from salivary samples obtained from infants.
Time Frame
Through study completion: at intervention start (Baseline, T0), 2 months after intervention start (post-intervention, T1), 3 months after intervention end (follow-up, T2), and 6 months after intervention end (follow-up, T3)
Other Pre-specified Outcome Measures:
Title
Feasibility and acceptability
Description
Mothers included in the two arms will rate feasibility and acceptability of the respective intervention received.
Time Frame
Through study completion, 2 months after intervention start (post-intervention, T1)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
3 Months
Maximum Age & Unit of Time
18 Months
Accepts Healthy Volunteers
No
Eligibility Criteria
ELIGIBILITY CRITERIA FOR INFANTS Inclusion Criteria: Infants with equivalent age range 3-to-18-months Mild to moderate psychomotor delay Exclusion Criteria: Presence of severe sensorial (auditory, visual) deficits Genetic syndrome with known functional implications for the epigenetic regulation of target genes ELIGIBILITY CRITERIA FOR MOTHERS Inclusion Criteria: Mastery of Italian language Age > 18 years Living with the father of the infant Exclusion Criteria: Documented mental disorder Documented disability
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Rosario Montirosso, PsyD
Organizational Affiliation
IRCCS E. Medea
Official's Role
Principal Investigator
Facility Information:
Facility Name
IRCCS E. Medea
City
Bosisio Parini
State/Province
Lecco
ZIP/Postal Code
23842
Country
Italy
Facility Name
Università degli Studi di Brescia
City
Brescia
ZIP/Postal Code
25123
Country
Italy
Facility Name
Fondazione Istituto Neurologico Casimiro Mondino
City
Pavia
ZIP/Postal Code
27100
Country
Italy

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
32699128
Citation
Montirosso R, Rosa E, Giorda R, Fazzi E, Orcesi S, Cavallini A, Provenzi L; Early Intervention Study Group. Early Parenting Intervention - Biobehavioral Outcomes in infants with Neurodevelopmental Disabilities (EPI-BOND): study protocol for an Italian multicentre randomised controlled trial. BMJ Open. 2020 Jul 21;10(7):e035249. doi: 10.1136/bmjopen-2019-035249.
Results Reference
derived

Learn more about this trial

Early Parenting Intervention: Bio-behavioral Outcomes in Infants With Neurodevelopmental Disabilities

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