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Evaluation of an Early Preventive and Educational Care Pathway for Moderate and Late Preterm Infants. A Randomized Controlled Study (PREKINOU)

4. November 2026 aktualisiert von: University Hospital, Caen

Prematurity is associated with a high risk of neurodevelopmental disorders (NDDs). The prognosis for moderate and late preterm infants (32 to <37 weeks of gestational age) is better than that for very preterm infants (<32 weeks of gestational age).

According to the French National Authority for Health (Haute Autorité de Santé, HAS), moderate and late preterm (MLPT) infants are at moderate risk of NDDs. However, although their risk is lower than that of very preterm infants, it remains significant. Recent research has challenged the misconception that MLPT births are associated with little or no increase in developmental delays compared with full-term births. The risk of NDDs is two to three times higher in these infants than in infants born at term. Prematurity, regardless of its degree, affects the motor and cognitive performance of children born preterm. Impaired neurological development persists at different follow-up ages.

Moderate and late preterm infants account for 85% of all preterm births. Consequently, the number of infants with NDDs is substantial, highlighting the need for appropriate care to limit the impact on the healthcare system.

When an NDD is suspected, the HAS recommends providing parental guidance to help parents initiate activities at home while awaiting the implementation of early intervention. However, these children currently receive no standardised follow-up. The lack of specific assessment of MLPT infants, due to underestimation of their neuromotor risk, leads to delays in care. These delays may result in delayed neuromotor development and potentially long-term sequelae. Yet interventions initiated before discharge from the neonatal unit have the greatest positive impact on the neuromotor development of preterm infants.

Parental education is an effective early intervention strategy. It provides a significant opportunity to improve young children's motor, language, cognitive and socio-emotional development, as well as attachment. It also helps parents develop a better understanding of their infants and promotes parent-infant interactions.

We hypothesise that an early preventive care pathway (PREKINOU) could improve the motor development scores of MLPT infants at 9 months of corrected age.

The objective of the study is to evaluate the effectiveness of an early preventive and educational care pathway (PREKINOU) on the motor development of MLPT infants at 9 months of corrected age (41 weeks ± 14 days), compared with standard care.

This study will include 92 infants born moderately or late preterm. The infants will be randomised into two groups. Infants in the experimental group (n = 46) will follow the PREKINOU pathway in addition to standard care and mandatory medical examinations, both in the maternity unit and after discharge home, until 13 weeks of corrected age (CA).

At 9 months of corrected age (41 weeks ± 14 days), infants in both the experimental and control groups will undergo a blinded assessment using the motor, cognitive and language subscales of the Bayley Scales of Infant and Toddler Development, Fourth Edition (Bayley-4). The assessment will be conducted by a psychomotor therapist trained in the administration of this scale.

Parents' perceptions of their ability to care for their infants will also be assessed at 9 months of corrected age using the Maternal Perceived Parental Self-Efficacy questionnaire (PMP-SE).

The level of parental engagement in the experimental group will be measured using logbooks. Parental support for the development of infants in both the experimental and control groups will be assessed at 9 months of corrected age using a questionnaire.

Studienübersicht

Status

Noch keine Rekrutierung

Bedingungen

Intervention / Behandlung

Studientyp

Interventionell

Einschreibung (Geschätzt)

92

Phase

  • Unzutreffend

Teilnahmekriterien

Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.

Zulassungskriterien

Studienberechtigtes Alter

7 Monate bis 8 Monate (Kind)

Akzeptiert gesunde Freiwillige

Nein

Studienberechtigte Geschlechter

Alle

Beschreibung

Inclusion Criteria:

  • Birth between 32 weeks + 0 days and 36 weeks + 6 days of gestational age at Flers Hospital or Caen University Hospital (CHU de Caen).
  • Maternal and paternal age ≥ 18 years.
  • At least one parent present in the hospital for more than 3 hours per day.
  • Residence within a 60-kilometre radius of the place of birth.
  • Parents' ability to understand and communicate in French, both orally and in writing.
  • Written informed consent signed by the legal representatives holding parental responsibility.
  • Affiliation with a social security system.

Exclusion Criteria:

  • Suspected hypoxic-ischaemic encephalopathy requiring therapeutic hypothermia.
  • Perinatal arterial ischaemic stroke, diagnosed between 20 weeks of fetal life and 28 days after birth.
  • Abnormal brain growth: microcephaly, defined as a head circumference ≤ -2 standard deviations (SD) at birth and subsequently confirmed, or macrocephaly ≥ +3 SD for gestational age, persisting after a second measurement.
  • First-degree family history of severe neurodevelopmental disorders (sibling or parent).
  • Symptomatic congenital cytomegalovirus infection or other congenital infections affecting the fetus, including toxoplasmosis, Zika virus infection and rubella.
  • Bacterial or herpesvirus encephalitis and meningoencephalitis.
  • Complex congenital heart disease requiring surgery, including transposition of the great arteries and hypoplastic left heart syndrome.
  • Prenatal exposure to a major toxic agent, including certain antiepileptic drugs or severe alcohol exposure and/or exposure associated with signs of fetal alcohol spectrum disorder.
  • Major, prolonged and repeated surgery (cardiac, cerebral, abdominal or thoracic).
  • Cortical blindness or retinopathy of prematurity resulting in blindness.
  • Congenital musculoskeletal abnormality.
  • Chromosomal or genetic abnormality.
  • Infants born to mothers or fathers with documented histories of social problems (including child abuse, neglect or parental substance misuse) or mental illness.
  • Multiple pregnancy involving three or more premature infants.
  • Bronchopulmonary dysplasia with ongoing oxygen dependency after 36 weeks of gestational age.
  • Any gastrointestinal or other condition preventing the infant from being placed in the prone position.

Studienplan

Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.

Wie ist die Studie aufgebaut?

Designdetails

  • Hauptzweck: Verhütung
  • Zuteilung: Zufällig
  • Interventionsmodell: Parallele Zuordnung
  • Maskierung: Keine (Offenes Etikett)

Waffen und Interventionen

Teilnehmergruppe / Arm
Intervention / Behandlung
Experimental: Experimental group

Infants will receive early preventive and educational care pathway (PREKINOU) in addition to standard care and mandatory medical examinations

Specific early preventive and educational care pathway for moderately and late preterm (MLPT) infants.

Kein Eingriff: Control group

Infants will receive only standard care

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Motor subscale of the Bayley Scales
Zeitfenster: 9 month

Infants' motor development will be assessed at 9 months of corrected age (41 weeks ± 14 days) using the Bayley Scales of Infant and Toddler Development, Fourth Edition (2022).

Scores will be compared with the normative data from the French adaptation of the Bayley-4

9 month

Sekundäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Language and Cognitive Subscales of the Bayley-4
Zeitfenster: 9 months

Infants' language and cognitive development will be assessed at 9 months of corrected age (41 weeks ± 14 days) using the Bayley Scales of Infant and Toddler Development, Fourth Edition (2022).

Scores on the Cognitive and Language subtests will be compared with the normative data from the French adaptation of the Bayley-4.

9 months
General Movement Assessment
Zeitfenster: 13 weeks

General Movements (GMs) will be assessed on two occasions in the experimental group: immediately before discharge from hospital or the maternity unit, and at 13 weeks of corrected age (3 months). In the control group, GMs will be assessed only at 13 weeks of corrected age.

The Revised Motor Optimality Score (MOS-R) will be calculated for each infant during the video analysis of GMs performed at 13 weeks of corrected age

13 weeks
Maternal Perceived Parental Self-Efficacy Questionnaire (PMP-SE)
Zeitfenster: 9 months

Parents in both groups will complete this questionnaire at 9 months of corrected age (41 weeks ± 14 days).

9 months
Level of Parental Engagement
Zeitfenster: From enrollment to the end of the programme"

Parents will be asked to record the frequency of activities completed each week in logbooks .

Adherence to the educational programme will be classified as follows:

  • Excellent adherence: parents complete at least two activities per day, on 5 out of 7 days.
  • Good adherence: parents complete at least two activities per day, on 3 out of 7 days.
  • Poor adherence: parents complete fewer than two activities per day, on 3 out of 7 days.
From enrollment to the end of the programme"
Questionnaire on Parental Support for the Development of MLPT Infants
Zeitfenster: 9 months

To assess the impact of the PREKINOU pathway on parental support for infant development, parents will be asked to complete a questionnaire at the final assessment, at 9 months of corrected age (41 weeks ± 14 days).

The questionnaire will address the following areas: The infant's environment, Positioning and daily routines, Sensory and motor stimulation and responses and adaptations to the infant's needs.

9 months

Mitarbeiter und Ermittler

Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.

Ermittler

  • Hauptermittler: VIRGILE FILLION BROQUET, CMPR (Center for Physical Medicine and Rehabilitation) La Clairière

Studienaufzeichnungsdaten

Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.

Haupttermine studieren

Studienbeginn (Geschätzt)

1. Januar 2027

Primärer Abschluss (Geschätzt)

1. November 2030

Studienabschluss (Geschätzt)

1. November 2030

Studienanmeldedaten

Zuerst eingereicht

4. November 2026

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

4. November 2026

Zuerst gepostet (Tatsächlich)

10. November 2026

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Tatsächlich)

10. November 2026

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

4. November 2026

Zuletzt verifiziert

1. Oktober 2026

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

Arzneimittel- und Geräteinformationen, Studienunterlagen

Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt

Nein

Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt

Nein

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