Program Intensive Habilitation (PIH) for Young Children With Early Brain Damage (PIHMulti)
Primary Purpose
Brain Injuries, Cerebral Palsy, Motor Skills Disorders
Status
Recruiting
Phase
Not Applicable
Locations
Norway
Study Type
Interventional
Intervention
Program Intensified Habilitation
Habilitation as usual
Sponsored by
About this trial
This is an interventional treatment trial for Brain Injuries focused on measuring brain injury, cerebral palsy, motor disability, GMFCS level, Pedi-Cat, Family Empowerment scale, Parenting stress index
Eligibility Criteria
Inclusion Criteria:
- age 2 - 6 years at the start of the program
- a diagnosis of severe cerebral palsy or similar motor disability of non-progressive etiology (GMFCS level IV-V),
- being able to participate in group sessions
- having parents who want to take an active part in their child's training
- least one of the parents must speak fluent Norwegian or English.
Exclusion Criteria:
- children with progressive disorders
- co-morbidity like autism spectrum disorder, severe visual and hearing impairments or intractable epilepsy that worsen with physical activity.
Sites / Locations
- Sørlandet HospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Other
Arm Label
Intervention group
Control group
Arm Description
Half of the study participants will be randomized to the intensive habilitation program the first year of program. The second year of program this group of participants will be offered habilitation "as usual".
Half of the study participants will be randomized to "treatment as usual" the first year of program, then offered the intensive program during the second year ("stepped wedge design").
Outcomes
Primary Outcome Measures
Change in Pediatric Evaluation of Disability Inventory - Computer Adaptive Test (PEDI-CAT)
Primary evaluation measure for the child
Change in Family Empowerment Scale (FES)
Primary evaluation measure for the parents
Secondary Outcome Measures
Change in Gross motor function measure (GMFM-88)
Secondary evaluation measure for the child
Change in Parenting Stress Index (PSI)
Secondary evaluation measure for the parents
Full Information
NCT ID
NCT05093777
First Posted
September 28, 2021
Last Updated
January 1, 2023
Sponsor
Sorlandet Hospital HF
Collaborators
Haukeland University Hospital, St. Olavs Hospital, University Hospital of North Norway
1. Study Identification
Unique Protocol Identification Number
NCT05093777
Brief Title
Program Intensive Habilitation (PIH) for Young Children With Early Brain Damage
Acronym
PIHMulti
Official Title
Evaluation of a Norwegian Model of an Intensive Habilitation Program for Young Children With Early Brain Damage - a Multicentre Randomized Controlled Trial.
Study Type
Interventional
2. Study Status
Record Verification Date
January 2023
Overall Recruitment Status
Recruiting
Study Start Date
October 10, 2021 (Actual)
Primary Completion Date
March 31, 2024 (Anticipated)
Study Completion Date
March 31, 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Sorlandet Hospital HF
Collaborators
Haukeland University Hospital, St. Olavs Hospital, University Hospital of North Norway
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief 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.
Detailed Description
Evidence-based knowledge about the effects of intensive training programs for children with severe early brain damage is limited since research on this topic has methodological weaknesses and shows conflicting results. As intensive training programs require extensive efforts from the child, parents and professionals and represent major costs, the importance of scientifically proven effects is considerable. This research project aims to measure the effects of an intensive habilitation program for young children with severe early brain damage on the child's adaptive, motor, language and social functioning and on parental empowerment, family functioning and stress. In this randomized controlled trial (RCT) 90 children will be divided into an intervention group participating in a Norwegian developed program of intensified habilitation of 12 months duration and a control group, who will receive "services as usual" during the same time period. Between-group analyses will then be performed. Due to a stepped wedge design, the control participants will then be offered training in year two of participation. Within-group analysis of results before and after training will then be performed for all participants. Standardized measures with high responsiveness in documenting intervention effectiveness will be used as primary outcome measures. Intensive training groups will be offered in all Health Regions in Norway and if successful be implemented as standard clinical practice.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Brain Injuries, Cerebral Palsy, Motor Skills Disorders, Empowerment, Parent-Child Relations, Parenting
Keywords
brain injury, cerebral palsy, motor disability, GMFCS level, Pedi-Cat, Family Empowerment scale, Parenting stress index
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Model Description
Randomized controlled trial (RCT) with blinded evaluation by independent researchers at baseline, at 12 months and at 24 months. A stepped-wedge design will be applied so that all study participants eventually will be offered the intervention program. Those who are randomized to control group in the first year of study, will be offered intensive training during the second year, and vice versa.
Masking
Outcomes Assessor
Masking Description
Blinded evaluation by independent researchers at baseline, at 12 months and at 24 months.
Allocation
Randomized
Enrollment
90 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Intervention group
Arm Type
Experimental
Arm Description
Half of the study participants will be randomized to the intensive habilitation program the first year of program. The second year of program this group of participants will be offered habilitation "as usual".
Arm Title
Control group
Arm Type
Other
Arm Description
Half of the study participants will be randomized to "treatment as usual" the first year of program, then offered the intensive program during the second year ("stepped wedge design").
Intervention Type
Other
Intervention Name(s)
Program Intensified Habilitation
Other Intervention Name(s)
PIH Multi
Intervention Description
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.
Intervention Type
Other
Intervention Name(s)
Habilitation as usual
Other Intervention Name(s)
Control
Intervention Description
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.
Primary Outcome Measure Information:
Title
Change in Pediatric Evaluation of Disability Inventory - Computer Adaptive Test (PEDI-CAT)
Description
Primary evaluation measure for the child
Time Frame
Change from baseline measure at 12 months and after 24 months
Title
Change in Family Empowerment Scale (FES)
Description
Primary evaluation measure for the parents
Time Frame
Change from baseline measure at12 months and after 24 months
Secondary Outcome Measure Information:
Title
Change in Gross motor function measure (GMFM-88)
Description
Secondary evaluation measure for the child
Time Frame
Change from baseline measure at 12 months and after 24 months
Title
Change in Parenting Stress Index (PSI)
Description
Secondary evaluation measure for the parents
Time Frame
Change from baseline measure at 12 months and after 24 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
2 Years
Maximum Age & Unit of Time
7 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
age 2 - 6 years at the start of the program
a diagnosis of severe cerebral palsy or similar motor disability of non-progressive etiology (GMFCS level IV-V),
being able to participate in group sessions
having parents who want to take an active part in their child's training
least one of the parents must speak fluent Norwegian or English.
Exclusion Criteria:
children with progressive disorders
co-morbidity like autism spectrum disorder, severe visual and hearing impairments or intractable epilepsy that worsen with physical activity.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jon S Skranes, MD PhD
Phone
99390285
Email
joskra@online.no
First Name & Middle Initial & Last Name or Official Title & Degree
Ida Vestrheim, MSc
Email
ida.vestrheim@sshf.no
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jon Skranes
Organizational Affiliation
Sørlandet Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Sørlandet Hospital
City
Kristiansand
ZIP/Postal Code
4626
Country
Norway
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jon Skranes
Phone
99390285
Email
joskra@online.no
First Name & Middle Initial & Last Name & Degree
Ida Vestrheim
Email
ida.vestrheim@sshf.no
12. IPD Sharing Statement
Plan to Share IPD
No
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Program Intensive Habilitation (PIH) for Young Children With Early Brain Damage
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