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Validity and Reliability of the PROprioception Measurement Tool (PROMT)

NCT05405881 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 99

Last updated 2023-12-01

No results posted yet for this study

Summary

This project assesses the feasibility, reliability, and validity of the PROMT in children with a UMN lesion. The study questions are: is the newly developed PROMT a feasible, reliable, and valid tool to assess lower limb proprioception in children with UMN lesions? Does the PROMT differ between children with UMN lesion and controlled neurotypically developing peers? Further, does the proprioception modalities assessed with the PROMT correlate with motor function in this group of children?

Conditions

  • Child Development
  • Upper Motor Neurone Lesion
  • Cerebral Palsy
  • Proprioceptive Disorders

Interventions

OTHER

Proprioception measurement tool

No intervention, as it is a psychometric properties study

Sponsors & Collaborators

  • Queen Margaret University

    collaborator OTHER

  • University Children's Hospital, Zurich

    lead OTHER

Principal Investigators

  • Hubertus JA van Hedel · University children's Hospital Zurich, Swiss children's Rehab

Study Design

Allocation
NON_RANDOMIZED
Purpose
OTHER
Masking
NONE
Model
CROSSOVER

Eligibility

Min Age
5 Years
Max Age
19 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2022-10-01
Primary Completion
2023-08-30
Completion
2023-08-30

Countries

  • Switzerland

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05405881 on ClinicalTrials.gov