Program Intensive Habilitation (PIH) for Young Children With Early Brain Damage

NCT05093777 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 93

Last updated 2026-05-07

No results posted yet for this study

Summary

By longitudinal, prospective research in children with neurodisabilities including severe motor impairments and their parents to explore the beneficial effects of participating in an intensive habilitation program on the child's adaptive functioning and parental empowerment in order to treat and reduce the consequences of early brain damage.

Conditions

  • Brain Injuries
  • Cerebral Palsy
  • Motor Skills Disorders
  • Empowerment
  • Parent-Child Relations
  • Parenting

Interventions

OTHER

Program Intensified Habilitation

The program is based on a holistic and family-centered concept, which acknowledges parents as experts on their child's abilities and needs. The program involves both parents and local professionals, and includes goal setting and goal-directed treatment targeted to the needs of the individual child. The program lasts for about one year and contains three in-patient group sessions over 2 weeks. In between the children are receiving individualized home training programs at home and in pre-school/kindergarten. The children train on a daily basis, both during the inpatient sessions and in the home setting.

OTHER

Habilitation as usual

When the participants are not joining the study year containing the intervention program, they will be offered habilitation services "as usual" administered by the primary health care services in the local community.

Sponsors & Collaborators

  • Haukeland University Hospital

    collaborator OTHER
  • St. Olavs Hospital

    collaborator OTHER
  • University Hospital of North Norway

    collaborator OTHER
  • Sorlandet Hospital HF

    lead OTHER_GOV

Principal Investigators

  • Jon Skranes · Sørlandet Hospital

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
CROSSOVER

Eligibility

Min Age
2 Years
Max Age
7 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-10-10
Primary Completion
2025-12-31
Completion
2025-12-31

Countries

  • Norway

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05093777 on ClinicalTrials.gov