Effectiveness of a Prenatal Educational Intervention to Prevent Positional Occipital Plagiocephaly
POP2019
1 other identifier
interventional
400
1 country
1
Brief Summary
Positional occipital plagiocephaly (POP) is a morphological abnormality of the cranium which, in the absence of early synostosis of the cranial sutures, is caused by external forces acting on the skull, which is highly malleable in newborns. The most common form of POP is the "acquired" type, which manifests around 2-3 months of age and reaches its peak severity around 4 months. The incidence of POP is 46.6% at 7-12 weeks of life, and 78.3% of cases are mild severity. In addition to being an aesthetic problem, POP can alter the first phase of a child's postural-motor development, causing postural asymmetries in the neck or spine, or asymmetries in the functional motor skills. Often, attention is only paid to the condition at a later stage, when the situation is very evident and often associated with other issues, resulting in longer, more expensive physiotherapy treatments and poorer outcomes. Recently, interest has emerged in the possibility of preventing POP: studies have been conducted showing that preventive and educational intervention with families on the most appropriate ways of caring for their babies after birth effectively reduces the incidence and severity of POP in the first months of life and that good nationwide training of healthcare professionals on this topic could help minimize public healthcare costs. The Specialist Interest Group (GIS) in Pediatric Physiotherapy of the AIFI Italian Association of Physiotherapists (AIFI) has produced a brochure for parents on the prevention of POP. Primary endpoint: to assess whether the educational intervention for the prevention of POP carried out by the physiotherapist, as part of the prenatal program, reduces the incidence of POP in infants at 3 months of age. Secondary endpoints: to assess whether the educational intervention is effective in preventing the problems often associated with POP (postural torticollis, muscle contracture in the neck, benign scoliosis, immaturity in axial control).
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Jan 2023
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 12, 2023
CompletedStudy Completion
Last participant's last visit for all outcomes
April 30, 2024
CompletedFirst Submitted
Initial submission to the registry
September 9, 2025
CompletedFirst Posted
Study publicly available on registry
September 19, 2025
CompletedSeptember 19, 2025
September 1, 2025
12 months
September 9, 2025
September 16, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Difference in the ODDI index measured with a craniometer
0,3 months post born
Secondary Outcomes (1)
Difference in number of children affected by torticollis, benign scoliosis, axial immaturity in control group and intervention group
0,3 months afther birth
Study Arms (2)
Experimental group
EXPERIMENTALParents who received the educational program on POP prevention
Standard of care
NO INTERVENTIONParents who do not received the educational program on POP prevention
Interventions
During a regular prenatal class meeting, parents belonging to this group received information about POP and how to prevent it (a presentation by a physiotherapist, a video shown to all centers participating in the study, practical demonstrations of activities using a doll, and a brochure with prevention tips). The children were then assessed at birth to rule out congenital disorders and at 3 months to detect any POP and associated postural problems. They were then sent a questionnaire to assess their perceived quality of the educational intervention carried out by the physiotherapist during the prenatal course.
Eligibility Criteria
You may qualify if:
- Participation of parents in the prenatal course at 34-38 weeks of gestation;
- Signing of the informed consent form;
You may not qualify if:
- parents (mother or both) aged \< 18 years;
- foreign parents with difficulty in understanding the Italian language and therefore giving informed consent to the study.
- In addition, children who present the following conditions at birth has been excluded from the study:
- prematurity with gestational age \< 36 weeks;
- neonatal distress;
- congenital occipital plagiocephaly - with cranial asymmetry measurable using a craniometer and ODDI (cranial asymmetry index) \> 112.6%;
- clavicle fractures;
- congenital clubfoot, metatarsus varus;
- congenital spinal and pelvic abnormalities.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Meyer Children's Hospital IRCCSlead
- Azienda Ospedaliero-Universitaria Careggicollaborator
- Azienda Ospedaliero-Universitaria di Parmacollaborator
- Ospedale Infermi Riminicollaborator
Study Sites (1)
Viola Fortini
Florence, FI, 50139, Italy
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- SUPPORTIVE CARE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Physiotherapist
Study Record Dates
First Submitted
September 9, 2025
First Posted
September 19, 2025
Study Start
January 1, 2023
Primary Completion
December 12, 2023
Study Completion
April 30, 2024
Last Updated
September 19, 2025
Record last verified: 2025-09
Data Sharing
- IPD Sharing
- Will not share