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Completed

NCT Number: NCT01092637

The TOBY Children Study

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.

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Key information

About this study

  • 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

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • participant in the TOBY Study

Exclusion criteria

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

Treatment and study plan

Primary outcomes

  1. Number of Survivors With an IQ > 84

    Time frame: 7 years 3 months

    IQ was measured using WPPSI III core tests

Secondary outcomes

  1. Number of Survivors Without Disability

    Time frame: 7 years 3 months

    IQ =>85, no neurological abnormalities, normal hearing, normal vision

  2. Number of Survivors With Cerebral Palsy

    Time frame: 7 years 3 months

    Number of participants diagnosed with Cerebral Palsy

Sponsors and collaborators

Lead sponsor

Imperial College London

Other

Collaborators

  • University of Oxford

Registry information

Official study title

School Age Outcomes Following a Newborn Cooling Trial

Important dates

Study start
2009
Primary completion
2013
Study completion
2014
First posted
Mar 25, 2010
Registry last updated
Jan 21, 2016

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

View the official ClinicalTrials.gov record (opens in a new tab)

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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