Status:

COMPLETED

Evaluation of the Impact of a Personalized Program of Adapted Physical Activates in Patients With Parkinson Disease

Lead Sponsor:

Centre Hospitalier Universitaire de Nīmes

Conditions:

Parkinson Disease

Eligibility:

All Genders

40-80 years

Phase:

NA

Brief Summary

Our study aims to compare the effects of a standard care plan to one using adapted physical activity in patients with Parkinson Disease. Using actigraphy as an evaluation measure will allow the collec...

Eligibility Criteria

Inclusion

  • The patient and their carer have given their free and informed consent and signed the consent form
  • The patient must be insured of the beneficiary of an insurance policy
  • The patient is available for the 6 month follow-up
  • The patient is between 40 and 80 years old
  • The patient has experienced symptoms of Parkinson Disease for at least 5 years and is in a stable state (no medical event or change of treatment in at least 1 month)
  • The functional impact and duration of fluctuations is ≥3 (MDS UPDRS)
  • The patient can walk autonomously, including using a technical aid
  • The patient does not have any regular physical activity excluding physiotherapy sessions
  • The patient has daily help from a caregiver

Exclusion

  • The subject and/or their caregiver is participating in another study
  • The subject and/or their caregiver is in a period of exclusion determined by a previous study
  • The patients is under judicial protection or state guardianship
  • It proves impossible to give the patient and/or the caregiver clear information
  • The patients and/or the caregiver reuses to sign the consent form
  • The patient is pregnant or breast feeding
  • The patient has anxiety or depression (Score HAD≥ 11/14), cardiac or respiratory failure (stress test), vesico-sphincter problems preventing normal practice of a physical activity, a contraindication to adapted physical activities
  • The patient cannot walk
  • Muscular tremor preventing the actigraphy measurement. Outside normal range values for UPDRS measures of: 3.15) postural tremor of the hands; 3.16) action tremor of the hands; 3.17) amplitude of rest tremor

Key Trial Info

Start Date :

January 10 2018

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

December 2 2019

Estimated Enrollment :

19 Patients enrolled

Trial Details

Trial ID

NCT03244813

Start Date

January 10 2018

End Date

December 2 2019

Last Update

January 27 2020

Active Locations (1)

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Page 1 of 1 (1 locations)

1

CHU Nimes

Nîmes, France, 30029