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Who we are

For policy-makers, medicine, research, pharma and funders: the situation in Austria and our plan for a centre of excellence.

Basis for the need

What early intervention achieves

Early intervention – especially before the first birthday – leads to:

  • better gross motor skills (e.g. higher GMFCS levels),
  • improved hand function (e.g. MACS levels),
  • a lower risk of contractures and malpositions.

Positive effects on cognition & communication

  • Children who receive early support show better language and cognitive development.
  • Programmes that are playful, close to everyday life and parent-centred are particularly effective.

Strengthening parental competence

  • Early intervention reduces parental stress and strengthens the sense of control and competence.
  • Parents report better interaction with their child and a higher quality of life.

Sources: Bundesgesundheitsblatt – effectiveness of early help, Measuring Early Intervention Effectiveness (CEI Australia)

The studies behind this – CP-EDIT, LEAP-CP and the Cochrane analysis – are described under Evidence & studies.

Effects of early diagnosis on therapy options

1. Early start of therapy: if CP is detected at just a few months of age (e.g. through GMA and HINE),

  • targeted physiotherapy (such as the COPCA or Bobath approach) can start early,
  • parents can be more closely involved, e.g. through coaching,
  • the period of highest neuroplasticity can be used optimally.

2. Individually tailored support: early detection makes it possible to tailor support plans individually – whether with regard to:

  • motor skills,
  • sensory integration,
  • cognition or communication.

3. Better prognoses: studies (also outside Scandinavia) show that children who receive early intervention often:

  • achieve a higher level of independence,
  • develop less severe secondary complications,
  • can more often be included in mainstream schools.

Living with cerebral palsy: the CP-North study

The CP-North study is a large-scale, multidisciplinary research project investigating how people with cerebral palsy (CP) and their families live in the Nordic countries – with a particular focus on quality of life, health, education, employment and social participation.

Overview

  • Duration: 2017–2021 (with ongoing analysis)
  • Countries: Sweden, Norway, Denmark, Finland and Iceland
  • Data: a combination of national health and social registers and the CP-specific register CPUP (except in Finland)
  • Participants: people with CP and their parents – compared to the general population

Aims of the study

  1. Analysing the life course: how does CP affect health, education, the labour market, income and mortality across the entire lifespan?
  2. Focus on parents: how does caring for a child with CP affect parents' lives – e.g. in terms of stress, employment or financial burden?
  3. Comparison between countries: how do the effects differ depending on the social system and health policy in the Nordic countries?

Results

1. Health & quality of life: People with CP more often have chronic pain, orthopaedic complications (e.g. hip dislocation, scoliosis) and limited mobility. Nevertheless, many report high life satisfaction when they are well cared for and socially included.

2. Education & employment:

  • Children with CP attend mainstream schools less often, especially with more severe motor impairments.
  • Adults with CP have considerably lower employment rates and incomes compared to the general population.
  • The differences are gender-related: women with CP are less often employed than men with CP.

3. Parents & families:

  • Parents of children with CP more often report psychological strain, reduced employment and financial losses.
  • Mothers are particularly affected, often reducing their working hours or leaving work altogether.

4. Country comparisons:

  • Despite similar social systems, there are differences between the Nordic countries – for example in school inclusion or support benefits.
  • Finland, which does not use a nationwide CP register like CPUP, serves as a comparison group in the study.

The study thus provides a unique long-term perspective on life with CP – and shows how important coordinated care, inclusion and family-friendly policies are.

Special features

  • The world's largest data collection on CP and family across the lifespan
  • Focus on social participation and social justice
  • The findings are intended to help improve care systems – not only in Scandinavia but internationally

Sources: BMJ Open – CP-North protocol, Lund University, Arcada research overview

The situation in Austria

In Austria, GMA is increasingly used in neonatal units and developmental clinics, for example at centres such as AKH Vienna or the children's rehab centre Wildbad. Programmes such as “Early Steps” (in Vienna) are also based on family-centred early intervention models – similar to the CP-EDIT study.

However, comprehensive, structured use (as in the Danish study) is not yet standard everywhere. There is great potential to learn from models such as CP-EDIT – in screening, interdisciplinary early intervention, evidence-based therapy options or parent coaching.

AI has great potential, for example in gait analysis: instead of collecting data at isolated points and reacting to it, AI support makes it possible to compare large amounts of data, recognise patterns and intervene in time when deterioration threatens.

MedUni Vienna is currently researching this: model-cp.univie.ac.at