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PaREnting ProgrAm to Enhance PREterm Infants' Health and Development (PREPARE Trial)

Not Applicable
Active, not recruiting
Conditions
Behavioral Assessment of Children
Early Intervention
Interventions
Behavioral: Comprehensive structured parent intervention
Registration Number
NCT04783220
Lead Sponsor
American University of Beirut Medical Center
Brief Summary

Preterm infants are at high risk of developmental delay or disabilities and they do benefit from early intervention programs. Many programs aiming at improving preterm infants' developmental outcome have been proposed with mixed results. In low to middle-income countries, clinically relevant and effective low cost interventions empowering parents have yet to be established.

Detailed Description

Education and intervention programs targeting parents of premature infants are lacking in low to middle income countries (LMIC) and in Arabic countries in particular. The main concept of this proposal is to develop a program in Arabic for parents of premature infants with the aim to increase their knowledge about short and long term problems of prematurity, increase their involvement in the care during their stay in the neonatal intensive care unit (NICU) and promote responsive and sensitive parenting in the NICU and after discharge. This is to empower parents and have them become active contributors to enhancing their infant's development through play activities and tracking of developmental milestones.

Recruitment & Eligibility

Status
ACTIVE_NOT_RECRUITING
Sex
All
Target Recruitment
72
Inclusion Criteria
  • Couplets of parents and their preterm infants admitted to the NICU, who are <35 weeks gestation at birth and who are deemed medically stable by their treating neonatologist.
Exclusion Criteria
  • Infants with significant neurologic disorder precluding meaningful interaction with the parents as determined by the neurologist
  • Infants with major congenital anomalies precluding meaningful interaction with the parents as determined by the neurologist
  • Infants with systemic medical and/ or surgical conditions precluding interaction with the parents, other than preterm-related intraventricular hemorrhage (IVH) and periventricular leukomalacia (PVL).
  • Parental refusal to participate
  • Absence of clearance from the neonatologist
  • Infants planned to be transferred to another facility for their NICU care.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
InterventionComprehensive structured parent interventionThe parents of babies in this group will receive an educational and intervention program
Primary Outcome Measures
NameTimeMethod
Child developmental outcome9 months

The developmental outcome of preterm children will be assessed using the Ages and Stages Questionnaire at 9 months of corrected age.

The ASQ-3 covers 5 area of child development : Gross Motor, Fine Motor, Problem Solving, Personal-Social, Communication.

Scores for each area should range between minimum 0 and maximum 60. Higher scores indicate that the child is developing properly.

Secondary Outcome Measures
NameTimeMethod
Physiological state- Respiratory rate1 year

Physiological parameters including respiratory rate will be retrieved from the bedside monitors.

Physiological state - Oxygen saturation1 year

Physiological parameters including oxygen saturation will be retrieved from the bedside monitors.

Neurobehavioral state1 year

Behavioral state will be assessed by a cerified trained developmental specialist using a 7-point score that include: (i) Quiet/deep sleep, (ii) Active sleep, (iii) Awake State, (iv) drowsy, (v) quiet alert, (vi) active alert, (vii) crying

Parental Knowledge assessmentBefore hospital discharge

Parental knowledge assessment test will be administered before and after the education sessions using 10 true/false questions regarding topics addressed in the sessions.

Parental stress1 year

The Arabic parenting stress index short form questionnaire will be used. The PSI-SF is a self-administered questionnaire and consists of 36 items divided into three subscales of 12 items each: parental distress, parent-child dysfunctional interaction and difficult child.

For each subscales scores ranges should be between 12 and 60. For the total stress score , the minimum score is 36 and the maximum is 180. Higher scores mean more depressive symptoms.

Behavioral parenting activities1 year

A questionnaire derived from the UNICEF MICS 6 questionnaire will be used. MICS or "MULTIPLE INDICATOR CLUSTER SURVEY" is a tool used to assess the activities of parents with their infants.

Parents perceptions1 year

The Perceived Maternal Parenting Self-Efficacy questionnaire is a standardized valid and reliable instrument to assess parent's perceptions of their ability to care for their infants.

PMP-SE is composed of 20 items divided into four subscales: care taking procedures, evoking behaviours, reading behaviours or signalling, and situational beliefs.

Those items are formulated as statements using a five-point Likert scale. Scoring ranges from 20 to 80 where a higher score indicates a higher self-efficacy.

Trial Locations

Locations (1)

American University of Beirut

🇱🇧

Beirut, Hamra, Lebanon

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