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Developmental Care Program in Neonatal Intensive Care Unit (CIN)

Primary Purpose

Premature Birth

Status
Enrolling by invitation
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
Family Education and Active Listening
Family Education
Sponsored by
University of Pisa
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Premature Birth focused on measuring Family-Centered Care, Neonatology, Early intervention, Counseling

Eligibility Criteria

1 Week - 10 Weeks (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Parents of preterm <34 weeks without brain lesion

Exclusion Criteria:

  • Parents of infants with brain Lesions
  • Parents of clinically unstable infants, based on standard medical evaluation of preterm infants (eg: children with mechanical ventilation or under sedation)
  • Parents of infants with genetic-malformative conditions
  • Parents with severe psychiatric disorders

Sites / Locations

  • IRCCS Fondazione Stella Maris

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Family Education Only

Family Education and Active Listening

Arm Description

Family Education Only. Parents will be asked to participate in an evidence based program s that includes 6-8 visits with a a trained healthcare provider. This program of early intervention based on the promotion of the parent-child relationship through the recognition of behavioral states, methods of interaction, facilitation strategies in the relationship. Active listening Visits includes a cycle of 5-6 consecutive meetings lasting about an hour. The meetings will take place in a defined and dedicated space (private room) or if possible (if no other parents are present) at the baby's cradle. The meeting will take place between a single parent and a trained direct operator. This is not a psychotherapeutic intervention but a support that is provided to the parent. The support is mainly based on active listening, on the problems posed by the parent and on the subject's empowerment.

Family Education and Active Listening. Parents of infants will be asked to participate in an evidence based program for parents of NICU infants that includes 6-8 visits with a a trained healthcare provider operator. This evidence-based program of early intervention based on the promotion of the parent-child relationship through the recognition of behavioral states, methods of interaction, facilitation strategies in the relationship. The program takes its conceptual basis from the Mother Infant Transaction Program (MITP). It involves about 6 meetings (1-2 a week) of 30-45 minutes that are carried out during the hospitalisation in the NICU directly at the child's bed between the operator and one or both parents.

Outcomes

Primary Outcome Measures

Parent Infant interaction behaviours coding
Video footage of key vocal, facial, and motor parental and infant interactive behaviours are analysed using micro coding system.
Parent Infant interaction behaviours coding
Video footage of key vocal, facial, and motor parental and infant interactive behaviours are analysed using micro coding system.
Parent Infant interaction behaviours coding
Video footage of key vocal, facial, and motor parental and infant interactive behaviours are analysed using micro coding system.
Developmental outcome assessment
Bayley Scales of Infant Development Third Edition will be conducted including the Cognitive, Language (Receptive & Expressive), Motor (Gross & Fine), Social-Emotional and Adaptive sub scales. Each sub scale score will be calculated based on the age (months of age) of the infant at the time assessment. Higher scores mean a better outcome.

Secondary Outcome Measures

Family well-being questionnaires
The Infant Toddler Quality of Life QuestionnaireTM (ITQOL)
Family well-being questionnaire
Edinburg Postnatal Depression Scale (EPDS)
Family well-being questionnaire
Depression Anxiety Stress Scale (DASS-21)
Family well-being questionnaire
Coping Orientation to Problems Experienced (COPE - NVI)

Full Information

First Posted
September 15, 2022
Last Updated
October 6, 2022
Sponsor
University of Pisa
Collaborators
Azienda Ospedaliero, Universitaria Pisana, IRCCS Fondazione Stella Maris
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1. Study Identification

Unique Protocol Identification Number
NCT05573945
Brief Title
Developmental Care Program in Neonatal Intensive Care Unit
Acronym
CIN
Official Title
Developmental Family Centred Care Program in Neonatal Intensive Care Unit
Study Type
Interventional

2. Study Status

Record Verification Date
October 2022
Overall Recruitment Status
Enrolling by invitation
Study Start Date
May 10, 2022 (Actual)
Primary Completion Date
April 30, 2024 (Anticipated)
Study Completion Date
December 31, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Pisa
Collaborators
Azienda Ospedaliero, Universitaria Pisana, IRCCS Fondazione Stella Maris

4. Oversight

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

5. Study Description

Brief Summary
This project is a Randomised Clinical Trial that includes a family centred education intervention and/or non-directive active listening counselling intervention with families of preterm infants at risk for sensori-motor disorders.
Detailed Description
Preterm babies, specifically with gestational age < 33+6 weeks, will be recruited and assigned (randomized) into an a Family Education + Active Listening Group (intervention A) or a Family Education Only Group (intervention B). When the clinical condition of the child is stable the parents are approached for consent and randomised. All families (in intervention A and intervention B) will receive the evidence-based program of Family Education which is based on the promotion of the parent-child relationship through the recognition of behavioral states, methods of interaction, facilitation strategies in the relationship. It takes its conceptual basis from the Mother Infant Transaction Program (MITP). It is a specific and re-adapted version for the preterm infant hospitalized in NICU The family education sessions involve about 6 meetings (1-2 a week) of 30-45 minutes that are carried out during the hospitalization in the NICU directly at the child's bed between the operator and one or both parents. Each meeting involves the discussion of one of the following topics. The Families in intervention group A will also receive 4-6 weekly meetings with a psychologist for an active listening counselling session.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Premature Birth
Keywords
Family-Centered Care, Neonatology, Early intervention, Counseling

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Two intervention groups, Randomised Controlled Trial
Masking
Outcomes Assessor
Masking Description
Double (Investigator, Outcomes Assessor) Investigator and Outcomes assessors are blind to the group assignment of the infant. Care provider (Parents and Research staff supporting parents in intervention can not be masked to the group assignment).
Allocation
Randomized
Enrollment
70 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Family Education Only
Arm Type
Experimental
Arm Description
Family Education Only. Parents will be asked to participate in an evidence based program s that includes 6-8 visits with a a trained healthcare provider. This program of early intervention based on the promotion of the parent-child relationship through the recognition of behavioral states, methods of interaction, facilitation strategies in the relationship. Active listening Visits includes a cycle of 5-6 consecutive meetings lasting about an hour. The meetings will take place in a defined and dedicated space (private room) or if possible (if no other parents are present) at the baby's cradle. The meeting will take place between a single parent and a trained direct operator. This is not a psychotherapeutic intervention but a support that is provided to the parent. The support is mainly based on active listening, on the problems posed by the parent and on the subject's empowerment.
Arm Title
Family Education and Active Listening
Arm Type
Active Comparator
Arm Description
Family Education and Active Listening. Parents of infants will be asked to participate in an evidence based program for parents of NICU infants that includes 6-8 visits with a a trained healthcare provider operator. This evidence-based program of early intervention based on the promotion of the parent-child relationship through the recognition of behavioral states, methods of interaction, facilitation strategies in the relationship. The program takes its conceptual basis from the Mother Infant Transaction Program (MITP). It involves about 6 meetings (1-2 a week) of 30-45 minutes that are carried out during the hospitalisation in the NICU directly at the child's bed between the operator and one or both parents.
Intervention Type
Behavioral
Intervention Name(s)
Family Education and Active Listening
Other Intervention Name(s)
Intervention A
Intervention Description
Bedside intervention directly with infant with trained healthcare providers and parents. Includes family education meetings completed with individual infant parent/s and trained operator. In addition, weekly meetings of parent/s with a psychologist in a private location for an active listening counselling session.
Intervention Type
Behavioral
Intervention Name(s)
Family Education
Other Intervention Name(s)
Intervention B
Intervention Description
Bedside intervention directly with infant with trained healthcare providers and parents. Includes family education meetings completed with individual infant parent/s and trained operator.
Primary Outcome Measure Information:
Title
Parent Infant interaction behaviours coding
Description
Video footage of key vocal, facial, and motor parental and infant interactive behaviours are analysed using micro coding system.
Time Frame
1 months corrected age
Title
Parent Infant interaction behaviours coding
Description
Video footage of key vocal, facial, and motor parental and infant interactive behaviours are analysed using micro coding system.
Time Frame
3 months corrected age
Title
Parent Infant interaction behaviours coding
Description
Video footage of key vocal, facial, and motor parental and infant interactive behaviours are analysed using micro coding system.
Time Frame
6 months corrected age
Title
Developmental outcome assessment
Description
Bayley Scales of Infant Development Third Edition will be conducted including the Cognitive, Language (Receptive & Expressive), Motor (Gross & Fine), Social-Emotional and Adaptive sub scales. Each sub scale score will be calculated based on the age (months of age) of the infant at the time assessment. Higher scores mean a better outcome.
Time Frame
12 months corrected age
Secondary Outcome Measure Information:
Title
Family well-being questionnaires
Description
The Infant Toddler Quality of Life QuestionnaireTM (ITQOL)
Time Frame
Before discharge from the Neonatal Unit (on average at 5 weeks post term age), 3, 6, 12 months corrected age
Title
Family well-being questionnaire
Description
Edinburg Postnatal Depression Scale (EPDS)
Time Frame
Before discharge from the Neonatal Unit (on average at 5 weeks post term age), 3, 6, 12 months corrected age
Title
Family well-being questionnaire
Description
Depression Anxiety Stress Scale (DASS-21)
Time Frame
Frame: Before discharge from the Neonatal Unit (on average at 5 weeks post term age), 3, 6, 12 months corrected age
Title
Family well-being questionnaire
Description
Coping Orientation to Problems Experienced (COPE - NVI)
Time Frame
Before discharge from the Neonatal Unit (on average at 5 weeks post term age), 3, 6, 12 months corrected age
Other Pre-specified Outcome Measures:
Title
General Movements (GM)
Description
The General Movements Assessment (GMA), an observation of infant spontaneous movements will be completed and scored based on a standard protocol of GMA. The observation allows for the understanding of the neurological risk category for neuromotor difficulties.
Time Frame
10-16 weeks corrected age

10. Eligibility

Sex
All
Minimum Age & Unit of Time
1 Week
Maximum Age & Unit of Time
10 Weeks
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Parents of preterm <34 weeks without brain lesion Exclusion Criteria: Parents of infants with brain Lesions Parents of clinically unstable infants, based on standard medical evaluation of preterm infants (eg: children with mechanical ventilation or under sedation) Parents of infants with genetic-malformative conditions Parents with severe psychiatric disorders
Facility Information:
Facility Name
IRCCS Fondazione Stella Maris
City
Pisa
State/Province
PI
ZIP/Postal Code
56125
Country
Italy

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
There is no plan to share the Individual Participant Data

Learn more about this trial

Developmental Care Program in Neonatal Intensive Care Unit

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