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OpenTrials
Completed

NCT Number: NCT05930522

Psychomotor Performance of Preterm Infants

The first part involved 120 children in grades II and III of elementary schools. From this group, children were qualified for the second part of the study - 35 randomly selected children born on time (BoT) and 35 children born before 35 weeks of pregnancy (PB). EUROFIT tests, Vienna Tests and postural stability tests were carried out in both groups.

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Key information

Age range

7 year–9 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Gdansk University of Physical Education and Sport

Gdansk, Pomeranian Voivodeship, 80-336, Poland

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • preterm born (PB): born before 35 weeks of gestation
  • both groups: aged 7-9 y during the research project

Exclusion criteria

  • musculoskeletal injuries
  • neurological disorders or other CNS damage

Treatment and study plan

Primary outcomes

  1. Eurofit test

    Time frame: 20 minutes

    Motor abilities

  2. Biodex Balance System SD

    Time frame: 15 minutes

    Static and dynamic postural stability

  3. Vienna Test

    Time frame: 15 min minutes

    Speed reactions

Sponsors and collaborators

Lead sponsor

Gdansk University of Physical Education and Sport

Other

Registry information

Official study title

Psychomotor Performance of Preterm Infants Born Between 24 and 35 Weeks of Gestation

Important dates

Study start
2018
Primary completion
2020
Study completion
2020
First posted
Jul 5, 2023
Registry last updated
Sep 26, 2023

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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