Actively Recruiting

Age: 15Years - 25Years
All Genders
NCT06090383

Feasibility and Discriminant Validity of Monitoring Movement Behavior of Adolescents With Cerebral Palsy

Led by Rigshospitalet, Denmark · Updated on 2025-06-22

25

Participants Needed

1

Research Sites

115 weeks

Total Duration

On this page

Sponsors

R

Rigshospitalet, Denmark

Lead Sponsor

U

University of Copenhagen

Collaborating Sponsor

AI-Summary

What this Trial Is About

A new artificial intelligence network has been developed to monitor real-world daytime and nighttime movement behavior of adolescents with cerebral palsy (CP). The network uses seven wearable sensors to recognize lying, sitting, and standing, as well as walking and movements of both arms and legs. This information can be useful for healthcare professionals to understand and influence change in movement behavior, leading to benefits for the health of adolescents with cerebral palsy. This study aims to examine the acceptability and technical dependability of monitoring the movement behavior of adolescents with cerebral palsy for 72 hours using wearable sensors. Additionally, the study aims to evaluate the network's ability to discriminate between control and individuals with CP, different subgroups of individuals with CP, as well as the incidence of sleep disturbance in the entire cohort.

CONDITIONS

Official Title

Feasibility and Discriminant Validity of Monitoring Movement Behavior of Adolescents With Cerebral Palsy

Who Can Participate

Age: 15Years - 25Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Clinical diagnosis of Cerebral Palsy at GMFCS-E&R levels I-V or typically developed without neurological impairment
  • Age between 15 and 25 years
  • Able to provide informed consent or have a legal guardian provide consent
Not Eligible

You will not qualify if you...

  • Unable to provide informed consent when another young adult with the capacity can provide similar data
  • Recent musculoskeletal surgery or injury with incomplete recovery of normal movement
  • Skin wounds in areas where sensors need to be attached

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University Hospital Copenhagen, Rigshospitalet

Copenhagen, Denmark, 2100

Actively Recruiting

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Research Team

I

Ivana Bardino Novosel, Ph.d. student

CONTACT

J

Jakob Lorentzen, Prof.

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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