Actively Recruiting

Phase Not Applicable
Age: 0 - 1Day
All Genders
NCT04380051

Evaluation of a Sensory-tonic Stimulation on Development of Parent-infant Interactions and Social Cognition in Very Premature Children

Led by CHU de Reims · Updated on 2026-02-19

120

Participants Needed

1

Research Sites

521 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Attachment is built primarily on the first interactions of the first 9 months of a baby's life. These first interactions and their effects of stress, pleasure and displeasure are retained to establish some of the baby's attachment behaviours and future relationships with others. Extreme prematurity strongly modify these first interactions between parents and child. Very preterm child is separated from his parents and is placed in a stressful, technical and potentially painful environment. Early interventions stimulate neuroplasticity and can positively affect the neurological development of very preterm infant. Tactile stimuli such as skin-to-skin contact and massages carried out by parents can be pleasant experiences that can support early interactions between parents and child.

CONDITIONS

Official Title

Evaluation of a Sensory-tonic Stimulation on Development of Parent-infant Interactions and Social Cognition in Very Premature Children

Who Can Participate

Age: 0 - 1Day
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Very preterm child born before 32 weeks of pregnancy
  • Parents agree to participate in the study
Not Eligible

You will not qualify if you...

  • Baby born before 25 weeks of pregnancy
  • Baby with birth weight less than 600 grams
  • Baby with congenital malformations
  • Baby with unstable blood circulation (hemodynamic instability)

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Chu Reims

Reims, France, 51092

Actively Recruiting

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Research Team

G

Gauthier Loron

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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