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Social Adjustment and Quality of Life After Very Preterm Birth

U

University Hospital Bonn (UKB)

Status

Completed

Conditions

Premature Birth
Low Birth Weight

Study type

Observational

Funder types

Other
Industry

Identifiers

NCT01163188
01ER0801

Details and patient eligibility

About

The major aim is the follow-up of the highest risk group (< 32 weeks gestation/ < 1500 birthweight) and their controls of the Bavarian Longitudinal Study (BLS) at the age of 24-27 years. The focus will be the identification of risk, protective and resiliency factors for cognitive and behavioural development and quality of life.

MRIs of the central nervous system will be conducted to examine aberrant activation patterns during the "attention network task" in stratified subgroups. Data driven MRI methods will be evaluated in relation to clinical, behavioural and developmental parameters.

Full description

The major aim is the follow-up of the highest risk group (< 32 weeks gestation/ < 1500 birthweight) and their controls of the Bavarian Longitudinal Study (BLS) at the age of 24-27 years. All probands have been assessed previously, neonatally and at additional six time points, the last time at the age of 12-13 years. The focus will be the identification of risk, protective and resiliency factors for cognitive and behavioural development and quality of life. On the basis of previously assessed data statistical modelling of child development until age 8.5 years will be conducted across the total range of gestation from 26-42 weeks to identify social factors amenable to intervention which could be associated with a positive development especially in moderate prematurity. In addition, cross-validation of the findings is planned by means of comparisons with three international studies (Millenium Cohort, GB; POPS, NL; EPICure, GB). MRIs of the central nervous system will be conducted to examine aberrant activation patterns during the "attention network task" in stratified subgroups. Data driven MRI methods will be evaluated in relation to clinical, behavioural and developmental parameters. In line with the objectives of funding there will be a further follow-up of the BLS to answer important questions regarding health and development of very small preterms.

Enrollment

520 patients

Sex

All

Ages

24 to 28 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • very low birth weight VLBW (< 1500g birthweight)and/ or
  • very preterm birth VPT (< 32 weeks of gestation)
  • Members of the Bavarian Longitudinal Study

Exclusion criteria

  • missing compliance

Trial design

520 participants in 2 patient groups

Proband
Description:
Very low birth weight children (\< 32 weeks of gestation) and/ or Very preterm children (\< 1500 g birthweight) of the Bavarian Longitudinal Study
Controls
Description:
Term born children of the Bavarian Longitudinal Study

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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