ClinicalTrials.Veeva

Menu

The TOBY Children Study

Imperial College London logo

Imperial College London

Status

Completed

Conditions

Cerebral Palsy
Hypoxia-Ischemia, Brain

Study type

Observational

Funder types

Other

Identifiers

NCT01092637
ISRCTN89547571
G0801320 (Other Grant/Funding Number)

Details and patient eligibility

About

The aim of this study is to determine the efficacy of therapeutic hypothermia following perinatal asphyxia on neurological and neuropsychological outcomes and also to assess academic attainment and any additional health, societal or educational costs associated with changes in outcome as a result of the intervention. This study will determine whether the apparent initial benefits of cooling are maintained in the longer term.

Perinatal asphyxia (a lack of oxygen occurring around the time of birth) may have long term consequences on brain functioning, which may be altered by treatment with hypothermia (cooling). Currently, there is no information on the effect of cooling on outcome beyond 18 months of age. We intend to assess at 6 - 7 years of age, the children that participated in the TOBY trial of whole body cooling following perinatal asphyxia and compare between the children that had received the cooling treatment soon after birth and those that were not treated with cooling, the number that survived with an intelligence quotient (IQ) greater than 84, the presence and severity of disabilities, educational attainment and the economic impact on families and service providers. If possible, children will be assessed in their school, with the option of alternative venues such as home or clinic if required.

During the assessment a paediatrician will conduct a neurological examination. A psychologist will administer psychometric tests to evaluate cognitive, behavioural and motor development. Questionnaires completed by parents and teachers will complete the data collection. Economic factors will also be assessed in the parent questionnaire.

Each child will have contact with the assessors during one school day with appropriate breaks. Assessments will take place over a period of 3 years.

Full description

  • Assessment tools used:

    • Wechsler Preschool and Primary Scale of Intelligence Third Edition (WPPSI-III; 2004) or Wechsler Intelligence Scales for Children
    • NEPSY Second Edition
    • Working Memory Test Battery for Children
  • Neurological examination by paediatrician

  • Questionnaire data from parents/guardians and teachers

Enrollment

280 patients

Sex

All

Ages

72 to 87 months old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • participant in the TOBY Study

Exclusion criteria

  • previously documented instruction not to approach for inclusion in further TOBY projects

Trial design

280 participants in 2 patient groups

Cooled
Description:
Child was allocated standard intensive care plus moderate whole body hypothermia treatment within 6 hours of birth
Non-cooled
Description:
Child was allocated standard intensive care only within 6 hours of birth

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems