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NCT Number: NCT05921422

Cognitive Functioning in Children and Adolescents With Cerebral Palsy

Background: Cerebral palsy (CP) is characterized by motor impairment but commonly involves more widespread difficulties, including cognitive impairment. However, cognitive impairment in CP - especially of a more subtle nature - is often overlooked, despite being associated with substantial academic, social, and emotional problems. In Denmark, the CP follow-up program (CPOP) includes systematic assessment of physical functions, but cognitive assessment is omitted. Prior to starting school, professionals evaluate the school readiness of children with CP, sometimes including a test of general cognitive functioning. Thereafter, cognitive assessments are rarely offered in mainstream schools (Folkeskolen) and can only be accessed if the difficulties are clearly disabling. Recent studies indicate that cognitive assessment needs to be implemented in the follow-up program for school children. For example, one study found that only 42% of students with CP complete mainstream school in Denmark, and international neurocognitive studies have found global cognitive difficulties (lower IQ) and specific impairments in visuo-spatial functions, executive functions, and processing speed in youth with CP. User organizations in the Nordic countries have called for action in recent years, leading to the development of a proposed cognitive follow-up program for children and adolescents with CP, the CPCog, which has yet to be evaluated and implemented in Denmark. Taken together, prior studies and patient experiences emphasize the need for systematic assessment of cognitive functioning in children and adolescents with CP to document the type and extent of cognitive difficulties, secure qualified intervention, and prevent the development of social and emotional problems.

Objective: The main purpose of this study is to characterize cognitive functioning in children and adolescents with CP in Danish mainstream schools. By documenting the extent and type of cognitive impairment associated with CP, we aim to inform future clinical practice and make recommendations for systematic assessment and intervention.

Method: The study is a cross-sectional study with 100 children and adolescents with CP (11-15 years). Each participant will undergo cognitive assessment with the core battery proposed in the Nordic CPCog protocol, including assessment of general cognitive functioning (intelligence), executive functions, and visuo-motor skills. Additionally, participants will undergo supplemental tests of memory, attention, fatigue, and symptoms of psychopathology. Cognitive assessments will take place at two sites: the Neurocenter for Children and Adolescents, Center for Rehabilitation of Brain Injury, and the Center for Clinical Neuropsychology, Children and Adolescents, Rigshospitalet, Copenhagen, Denmark. The project is carried out in collaboration between the neuropediatric and neuropsychological teams associated with the two sites of assessment, as well as the Center for Cerebral Palsy, Rigshospitalet, Aarhus University Hospital, CPOP, and an external advisory board including leading international CP experts.

Results: The CPCog-Youth-DK study will help characterize the cognitive difficulties associated with CP in children and adolescents in mainstream school, which will guide clinical practice and the development and implementation of systematic cognitive assessment and intervention programs. The cognitive assessment protocol will also be evaluated from the perspectives of children and adolescents with CP, parents, and professionals (e.g., assessors and school personnel) to evaluate whether the protocol is tolerable and helpful. Study results will be published in international, peer-reviewed journals, and will be made publicly available via other relevant platforms (such as the websites for the CP clinic at Rigshospitalet, Center for Rehabilitation of Brain Injury, and the Elsass Foundation). Several of the study investigators are directly involved in the current CP follow-up program in Denmark which will aid the process of turning our research into practice.

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Key information

Age range

11 year–15 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Center for Rehabilitation of Brain Injury (Center for Hjerneskade), Copenhagen, Denmark

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Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

CASE GROUP:

Inclusion criteria

  • 11-15 years old
  • Diagnosed with CP (irrespective of type and severity)
  • Attends a Danish mainstream school at time of enrollment

Exclusion criteria

  • Does not speak or understand Danish at the level necessary to participate (as evaluated by the research team)

CONTROL GROUP:

Inclusion criteria

  • 11-15 years old
  • Attends a Danish mainstream school at time of enrollment

Exclusion criteria

  • Does not speak or understand Danish at the level necessary to participate (as evaluated by the research team)
  • Diagnosed with CP (irrespective of type and severity), traumatic brain injury or other neurological disorder (e.g., epilepsy)

Treatment and study plan

Cognitive Assessment

Other

All participants will receive cognitive assessment with a core battery (CPCog) and a supplemental battery.

The core battery includes standardized tests of general cognitive functioning (intelligence) and visual-spatial abilities, as well as a questionnaire on executive functioning in daily life. The supplemental battery assesses attention, executive functioning, memory, fatigue, and symptoms of mental health issues (including symptoms of anxiety, depression, and attention deficit hyperactivity disorder/ADHD).

Primary outcomes

  1. Global cognitive functioning (IQ)

    Time frame: At first day of assessment

    General cognitive functioning as measured by the GAI from the Wechsler Intelligence Scale for Children, Fifth Edition (WISC-V)

  2. Visuo-spatial functioning

    Time frame: At first day of assessment

    Score from the Beery-Buktenica Developmental Test of Visual Motor Integration (Beery VMI)

  3. Executive functioning

    Time frame: At first day of assessment

    Cognitive regulation index score from the Behavior Rating Inventory of Executive Function - second edition (BRIEF-2), parent version.

Secondary outcomes

  1. Task switching ability

    Time frame: At second day of assessment

    Number of correct words named on the D-KEFS verbal fluency task, and completion time in seconds on the D-KEFS Trail Making task

  2. Attention

    Time frame: At second day of assessment

    Response sensitivity score (d') on the Test of Variables of Attention (T.O.V.A.)

  3. Verbal memory

    Time frame: At second day of assessment

    Scale scores of selected verbal subtests (Word Selective Reminding; Object Recall) from 6the Test of Memory and Learning, Second edition (TOMAL-2)

  4. Visual memory

    Time frame: At second day of assessment

    Scale scores of selected nonverbal subtests (Abstract Visual Memory; Visual Sequential Memory) from the Test of Memory and Learning, Second Edition (TOMAL-2)

  5. Working memory

    Time frame: At second day of assessment

    Working Memory Index score from the WISC-V

Other outcomes

  1. ADHD symptomatology

    Time frame: At second day of assessment

    Total scores of inattention, hyperactivity, and behavior scales of the ADHD-rs questionnaire

  2. Symptoms of autism spectrum disorder

    Time frame: At second day of assessment

    Index score from the Behavior Assessment System for Children, third edition (BASC-3), parent and child version

  3. Symptoms of emotional behavioral disturbance

    Time frame: At second day of assessment

    Index score from the Behavior Assessment System for Children, third edition (BASC-3), parent and child version

  4. Fatigue

    Time frame: At second day of assessment

    PedsQL MFS score

  5. Adaptive functioning

    Time frame: At second day of assessment

    General Adaptive Composite (GAC) score from the Adaptive Behavior Assessment System, Third Edition (ABAS-3)

Study contacts

Contact information is provided by the study sponsor or research team.

Camilla Funch Uhre, MSc, PhD

CONTACT

[email protected]

+4530537166

Christina Høi-Hansen, MD, PhD

CONTACT

[email protected]

+4535455095

Sponsors and collaborators

Lead sponsor

Rigshospitalet, Denmark

Other

Collaborators

  • Aarhus University Hospital
  • Center for Rehabilitation of Brain Injury (Center for Hjerneskade)
  • University of Copenhagen

Registry information

Acronym: CPCog-Youth-DK

Important dates

Study start
2023
Primary completion
2026
Study completion
2026
First posted
Jun 27, 2023
Registry last updated
Jun 27, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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