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Clinical Trials/NCT01092637
NCT01092637
Completed
Not Applicable

School Age Outcomes Following a Newborn Cooling Trial

Imperial College London1 site in 1 country280 target enrollmentSeptember 2009

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Cerebral Palsy
Sponsor
Imperial College London
Enrollment
280
Locations
1
Primary Endpoint
Number of Survivors With an IQ > 84
Status
Completed
Last Updated
10 years ago

Overview

Brief Summary

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.

Detailed 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

Registry
clinicaltrials.gov
Start Date
September 2009
End Date
July 2014
Last Updated
10 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • participant in the TOBY Study

Exclusion Criteria

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

Outcomes

Primary Outcomes

Number of Survivors With an IQ > 84

Time Frame: 7 years 3 months

IQ was measured using WPPSI III core tests

Secondary Outcomes

  • Number of Survivors Without Disability(7 years 3 months)
  • Number of Survivors With Cerebral Palsy(7 years 3 months)

Study Sites (1)

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