Actively Recruiting

Age: 0 - 3Years
All Genders
Healthy Volunteers
ID07296003

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

Led by Masaryk University · Updated on 2026-01-06

60

Participants Needed

3

Research Sites

52 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are investigating early motor behavior in infants to understand how it relates to their later psychomotor development. The study includes both preterm and full-term infants and aims to determine if early motor quality can predict later developmental outcomes. It also explores whether infants with similar early motor scores develop differently depending on their birth status, and if early therapy might improve outcomes for those with low motor scores. The study uses a combined retrospective and prospective observational design. It involves analyzing previously recorded videos of early spontaneous movements scored with the Motor Optimality Score - Revised (MOS-R). Caregivers are then contacted when the child reaches 18 and 36 months to complete questionnaires about motor skills, communication, sensory processing, and social behavior. Some infants with atypical early motor behavior may have received the Vojta method, a therapy using specific pressure points to improve motor control, although this therapy is not assigned by the study. Participants are involved through initial video recordings from routine care and later follow-up questionnaires completed by caregivers at 18 and 36 months. Researchers assess the association between early movement quality and later development in various domains. The study monitors developmental outcomes over several years, combining retrospective data with prospective follow-up to provide a comprehensive view of early predictors of neurodevelopmental trajectories.

CONDITIONS

Brief Title

Motor Development and Early Predictors of Psychomotor Outcomes in Preterm and Term Infants Assessed by MOS-R and Caregiver Questionnaire at 18 and 36 Months

Who Can Participate

Age: 0 - 3Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • The child was born either preterm or full-term.
  • 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.
Not Eligible

You will not qualify if you...

  • 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.

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

No additional visits; eligibility is based on existing video recordings and consent.

Diagnostic Evaluation

Duration - Retrospective review of recordings from the neonatal and early infant period

Participants' early spontaneous motor behavior and postural control are assessed using previously recorded videos collected during routine clinical examinations in infancy.

No visits; assessments are based on existing clinical video recordings.

Long-term Monitoring

Duration - From 18 to 36 months of age

Caregivers complete developmental questionnaires assessing motor, cognitive, sensory, and socio-emotional domains when the child reaches 18 and 36 months of age.

2 remote questionnaire completion points (at 18 and 36 months)

Trial Site Locations

Total: 3 locations

1

Nemocnice Pardubického kraje, a.s.

Pardubice, Czechia, Czechia, 53002

Actively Recruiting

2

Lentilka - integrated kindergarden and rehabilitation center

Pardubice, Česká Republika, Czechia, 530 02

Actively Recruiting

3

Lentilka - integrated kindergarden and rehabilitation center

Pardubice, Česká Republika, Czechia, 530 02

Actively Recruiting

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Research Team

L

Lukas Teply, Master degree

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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