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Preventive Osteopathic Treatment of Plagiocephaly (TOPP PLAGIO)

University Hospital Center (CHU) logo

University Hospital Center (CHU)

Status

Completed

Conditions

Axial Hypertony
Head Turn Preference
Positilonal Deformation of the Skull

Treatments

Procedure: manual therapy/osteopathy

Study type

Interventional

Funder types

Other

Identifiers

NCT03780920
RECHMPL18_0207

Details and patient eligibility

About

Positional cranial deformities (PCD), plagiocephaly and brachycephaly are a common reason for pediatric consultation, which has increased significantly since the recommendation to lay babies on their backs to prevent unexpected infant death (ILD). CPD is a source of concern for parents about their impact on psychomotor development and the aesthetic risk of deformity. The High Authority for Health (HAS) will soon put in place recommendations with a fact sheet for health professionals and the public. The aim of this research is to study whether early treatment of rotation disorders and hypertonia in newborns by manual osteopathic techniques would prevent the occurrence of positional deformities of the skull.

The main objective is to evaluate the effectiveness of an early osteopathic treatment on the rate of CPP (plagiocephalic and postural brachycephalia) at 4 months in newborns at risk.

the secondary objective is: to evaluate the effectiveness of an early osteopathic treatment on the quality of life of the child at 4 months.

Methodology: Controlled, randomized monocentric two-arm parallel study between (1) osteopathic follow-up and (2) osteopathy-free follow-up. The inclusion period will be 18 months and the follow-up period is 4 months.

Procedure: The two groups will be evaluated at 3 days and 4 months. The experimental group will benefit from an osteopathic treatment of 3 days of life to 4 months with a frequency of 3 to 4 sessions. Both groups will benefit from sleeping, carrying, positioning and stimulation advice.

The perspectives are:

  • the decrease in the prevalence of CPP after early osteopathic treatment.
  • Defining a decision algorithm for early osteopathic treatment.
  • Subject to recommendations on the indication of early osteopathic treatment in neonates at risk.

Enrollment

101 patients

Sex

All

Ages

3 to 11 days old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Newborn baby aged 3 days and until the maternity leave

  • Newborn with at least one risk factor for cranial deformity:

    • Newborn who received instrumental vaginal delivery.

    • Newborn presenting:

      • a preferential side,
      • global axial hypertonia,
      • Localized suboccipital hypertonia
    • Newborn presenting:

      • cranial deformity at birth,
      • a deformation of the face,
      • deformity of the trunk in scoliosis, comma or hyperextension

Exclusion criteria

  • Newborn with congenital muscular torticollis (managed directly in physiotherapy)

    • Premature neonate (<37SA)
    • Newborn with a malformation pathology
    • Newborn with craniosynostosis.
    • Newborn with a contraindication to the practice of osteopathy.

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

101 participants in 2 patient groups

Osteopathic treatment
Active Comparator group
Treatment:
Procedure: manual therapy/osteopathy
Control group
No Intervention group

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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