Status:

COMPLETED

Walking Pattern Characteristics in Normal Pressure Hydrocephalus

Lead Sponsor:

University of Zurich

Collaborating Sponsors:

ETH Zurich

Conditions:

Idiopathic Normal Pressure Hydrocephalus (INPH)

Eligibility:

All Genders

18-100 years

Phase:

NA

Brief Summary

20 patients who are diagnosed with NPH receive a set of 5 wearable gyroscopes (IMUs, ZurichMove sensors) for a period of 3 days for measurement and characterization of their walking in an ambulatory s...

Detailed Description

Temporary attachment of IMUs to wrists and ankles of the patients and probands for a period of three days and recording of movement during a 10 meter-walking test, 180° turnaround and during normal mo...

Eligibility Criteria

Inclusion

  • Age limits for the NPH patient group and the matched healthy vonunteers group are 60-100 years.
  • Age limits for the young healthy volunteers group are 18-40 years.
  • NPH patient group:
  • Informed Consent as documented by signature prior to any study related procedures or informed consent by a legal representative in case of cognitive deficits.
  • Male and female patients alike
  • Age between 60 and 100 years
  • Clinical suspect for NPH
  • Significant improvement (by more than 10%) in walking speed or endurance in a standardized CSF-TAP test (of at least 35 ml CSF).
  • Planned implantation of a VP shunt for NPH treatment (independently from the study).
  • Matched controls group:
  • Informed Consent as documented by signature prior to any study related procedures
  • Male and female patients alike (matched to group 1)
  • Age between 60 and 100 years (matched to group 1)
  • No clinical suspect for NPH or any other movement disorder
  • Young controls group:
  • Informed Consent as documented by signature prior to any study related procedures
  • Male and female patients alike (matched to group 1)
  • Age between 18 and 40 years
  • No clinical suspect for NPH or any other movement disorder

Exclusion

  • Enrolment of the investigator, his/her family members, employees and other dependent persons (only for patients; no exclusion criteria for controls),
  • Apparent or suspected movement disorder or other known disorder, which might affect normal standing or walking
  • Cardiovascular disorders, which might affect physical resilience
  • Pregnant women
  • Pre-menopausal state of female patients and probands in groups 1 and 2.
  • Children and adolescents

Key Trial Info

Start Date :

January 1 2018

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

April 25 2024

Estimated Enrollment :

60 Patients enrolled

Trial Details

Trial ID

NCT04702035

Start Date

January 1 2018

End Date

April 25 2024

Last Update

April 26 2024

Active Locations (1)

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Page 1 of 1 (1 locations)

1

Dept. of Neurosurgery, Zurich University Hospital

Zurich, Switzerland, 8091