CClinicalTrials.gg
Status unknownNCT06071000Updated Oct 6, 2023

Preschool Children Motor Development

An interventional study of Neuro-developmental stimulation (Neuro-vývojová stimulace). in Persisting Primitive Reflexes, sponsored by Charles University, Czech Republic. Status unknown. Open to participants aged 4 Years to 6 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2023-10-06.

Sponsored by Charles University, Czech Republic · Not applicable, Interventional, and Supportive care

The sponsor has not verified this record recently (last verified Jan 2023), so the status shown — last known as Not yet recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
80
Allocation
Randomized
Ages
4 Years to 6 Years
Sex
All
01

Study summary

The preschool age period is crucial for motor and cognitive development, which retention primary reflexes can negatively influence. Primary reflexes are fixed motor patterns controlled from developmentally lower areas of CNS and are necessary for delivery, survival or rudimentary movement activation during infancy and should be progressively inhibited. Primary reflexes' retention increases the risk of blocks for further cognitive and motor development in higher, mainly cortical areas. Children in preschool and school age with non-inhibited primary reflexes displayed a poor level of fundamental movement skills and worse attention, self-regulation or working memory capacity. Children with the problems above usually pass a movement program based on developmental kinesiology, like Neurodevelopmental stimulation (NVS). NVS contains exercises that simulate situations for adequate processing of the primary reflex and allow the brain to correct and inhibit this reflex. Even though in the Czech preschool environment, almost 13% of children with neurotypical development have significant positive responses to at least one primary reflex, there are no methods to inhibit primary reflexes to improve motor and cognitive development positively. Therefore, this project aims to find how the NVS intervention will influence the performance in the selected area of motor and cognitive development, with the follow-up three-month retesting. Population for this project are preschool children aged 4-6 years old.

02

Conditions studied

  • Persisting Primitive Reflexes

Keywords

  • motor development
  • fundamental motor skills
  • executive functions
  • neurodevelopmental
03

In context

Lead sponsor

Charles University, Czech Republic is the lead sponsor of 220 studies on the registry; 76 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
4 Years to 6 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • healthy

Exclusion criteria

Exclusion Criteria:

  • strong ADHD/learning disorders diagnosed
05

Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
80 participants (estimated)

Study arms

  • Experimental
    Experimental group

    Behavioral: Neuro-developmental stimulation (Neuro-vývojová stimulace).

  • No intervention
    Control group

Interventions

  • BehavioralNeuro-developmental stimulation (Neuro-vývojová stimulace).

    Neuro-developmental stimulation is exercise based intervention program that is focused on repeating reflex movements and thus inhibiting reflexive response.

06

What researchers measure

Primary outcomes

  1. TGMD-2

    Test of gross motor development

    Time frame: 8 months

  2. IDS / IDS-P

    Intelligence and Development Scale (preschool)

    Time frame: 8 months

  3. Primitive (primary) reflexes

    Tests for persisting (retained) primitive reflexes

    Time frame: 8 months

07

Study locations

No study locations are listed for this record.

08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 6, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT06071000
Lead sponsor
Charles University, Czech Republic
Responsible party
Sponsor
First posted
Oct 6, 2023
Start date
Mar 1, 2024 (estimated)
Primary completion
Jun 1, 2024 (estimated)
Completion
Sep 30, 2024 (estimated)
Last update
Oct 6, 2023

Study contacts

Adam Provazník
Contact
pro.vaz.nik@seznam.cz
774138660

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Jan 2023. You cannot join it, but the record below documents what was studied.

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