Clinical trial Recruiting at 3 sites Observational Ages Any age to 3

Early spontaneous movements and later psychomotor outcomes in preterm and full-term infants

Official title: A Longitudinal Observational Study of Early Spontaneous Motor Activity, Postural Control, and Motor Optimality Score (MOS-R) as Predictors of Psychomotor, Cognitive, and Sensory Development at 18 and 36 Months in Preterm and Term Infants, With Consideration of Early Therapeutic Intervention

Run by Masaryk University · NCT07296003 · Data updated 2026-11-12

This project will test whether the quality of early spontaneous movements in preterm and full-term infants predicts their motor, communication, sensory, and social development at 18 and 36 months.

More Neurodevelopmental Disorders trials

Quick facts

Study typeObservational
AgesAny age to 3 Years
SexAll
Enrollment60 (estimated)
SponsorMasaryk University
Academic / other
Locations3 sites (Pardubice, Czechia and 2 other locations)
StatusRecruiting
StartedApril 19, 2024
Main results expectedJanuary 1, 2027
Study endsJanuary 1, 2027
Registry record updatedNovember 5, 2026
Trial IDNCT07296003 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Infants (preterm or full-term) who have a usable early video recording of spontaneous movements from routine care and whose caregivers can complete follow-up questionnaires at around 18 and 36 months.

Probably not a fit

Infants without usable early movement recordings, those with severe congenital conditions that prevent movement assessment, or those who cannot be reached for follow-up are unlikely to benefit from this protocol's findings.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This combined retrospective–prospective observational project uses anonymized video recordings of infants' spontaneous movements from neonatal and outpatient physiotherapy visits, scored with the Motor Optimality Score–Revised and detailed general movement assessment. The retrospective component provides high-quality early movement data that cannot be re-created, while the prospective component contacts caregivers when children reach about 18 and 36 months to complete validated questionnaires on motor skills, communication, sensory processing, and socio-emotional functioning. The design compares outcomes between preterm and full-term infants with similar early motor scores and examines whether low early scores identify children who might benefit from early therapy. Statistical analysis will link early MOS‑R and movement patterns to later questionnaire-based developmental outcomes.

Why it matters

Potential benefit: If successful, clinicians could identify infants at higher risk for developmental delays earlier and offer timely therapy to improve outcomes.

How similar studies have gone: Previous work using the General Movements Assessment and MOS‑R has shown predictive links between early movement quality and later neurodevelopment, though evidence that early therapy based on these scores improves long-term outcomes remains limited.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* The child was born either preterm or full-term. Both groups are included in the study.
* The child completed a video recording of early movements during routine check-ups in the first months of life.
* The parents or legal guardians agree to participate and give informed consent.
* The child will be available for follow-up at around 18-36 months of age, when parents will complete a developmental questionnaire.

Exclusion Criteria:

* There is no usable video recording of the child's early spontaneous movements from the neonatal or early infant period.
* The child has a diagnosed medical condition that makes movement assessment impossible (for example, severe congenital anomalies or conditions preventing typical movement).
* Parents do not wish to participate or withdraw their consent.
* The child is not available for follow-up, meaning that the developmental questionnaire at 18-36 months cannot be completed.

Where it's running

  • Nemocnice Pardubického kraje, a.s.
    Pardubice, Czechia, Czechia
    Recruiting
  • Lentilka - integrated kindergarden and rehabilitation center
    Pardubice, Česká Republika, Czechia
    Recruiting
  • Lentilka - integrated kindergarden and rehabilitation center
    Pardubice, Česká Republika, Czechia
    Recruiting

Study contacts

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.