Physical Activity in Persons With Charcot-Marie-Tooth: Developing a Measurement Instrument

NCT04461613 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 20

Last updated 2021-02-24

No results posted yet for this study

Summary

The project will develop knowledge about physical activity in persons with Charcot-Marie-Tooth (CMT) in Norway. We plan to explore instruments to measure physical activity level for the target-group at the community level. We want to understand which type of activities, activity intensities and how persons with CMT perform habitual physical activity. Subsequently, a physical activity measurement instrument adapted to persons with CMT will be developed. This instrument can be used in a future intervention project to promote physical activity in this group.

Conditions

  • Hereditary Motor and Sensory Neuropathy
  • Charcot-Marie-Tooth
  • Polyneuropathies

Interventions

OTHER

Original IPAQ followed by a revised one.

Comparing two questionnaires (a revised version and an original International Physical Activity Questionnaire short form) with an activity diary.

OTHER

Revised IPAQ followed by an original one.

Comparing two questionnaires (a revised version and an original International Physical Activity Questionnaire short form) with an activity diary.

Sponsors & Collaborators

  • Norwegian National Advisory Unit on Rare Disorders (NKSD)

    collaborator UNKNOWN
  • University of Oslo

    collaborator OTHER
  • Foreningen for Muskelsyke

    collaborator UNKNOWN
  • Oslo University Hospital

    lead OTHER

Principal Investigators

  • Kristin Ørstavik, MD, Ph.D. · Oslo University Hospital

Study Design

Allocation
RANDOMIZED
Purpose
SCREENING
Masking
DOUBLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-09-15
Primary Completion
2021-03-31
Completion
2021-04-30

Countries

  • Norway

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 NCT04461613 on ClinicalTrials.gov