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Cardio-Respiratory Response of a Training Session Versus an Adapted Physical Activity Session (WIIRR)

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ClinicalTrials.gov Identifier: NCT03793504
Recruitment Status : Recruiting
First Posted : January 4, 2019
Last Update Posted : March 6, 2019
Sponsor:
Information provided by (Responsible Party):
University Hospital, Brest

Brief Summary:
the aim of this study is to show that training session with nintendo WII requires the same cardiorespiratory demand than training session on ergocycle or treadmill, traditionally used in pulmonary rehabilitation program.

Condition or disease
Pulmonary Disease

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Study Type : Observational
Estimated Enrollment : 20 participants
Observational Model: Cohort
Time Perspective: Prospective
Official Title: Cardio-Respiratory Response of an Exercise Training Session With Ergocycle or Treadmill Compared to an Adapted Physical Activity Session on a Wii, in Patients With Pulmonary Disease
Actual Study Start Date : January 2, 2019
Estimated Primary Completion Date : June 17, 2019
Estimated Study Completion Date : June 17, 2019



Primary Outcome Measures :
  1. compare heart rate between a training session on cycle or treadmill and a training session on Nintendo WII [ Time Frame: one day ]
    heart rate (pulse per minute) at the end of each session


Secondary Outcome Measures :
  1. compare dyspnea between a training session on cycle or treadmill and a training session on nintendo WII [ Time Frame: one day ]
    dyspnea (borg scale) at the end of each session

  2. compare lower limb muscle fatigue between a training session on cycle or treadmill and a training session on nintendo WII [ Time Frame: one day ]
    lower limb muscle fatigue (borg scale) at the end of each session

  3. compare pulse oxymetry (SpO2) between a training session on cycle or treadmill and a training session on nintendo WII [ Time Frame: one day ]
    SpO2 at the end of each session

  4. Compare the felt pleasure between a training session on cycle or treadmill and a training session on nintendo WII [ Time Frame: one day ]
    felt pleasure (likert scale) at the end of each session



Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population
patients with pulmonary disease admitted in pulmonary rehabilitation unit of CHU Brest
Criteria

Inclusion Criteria:

  • patients with pulmonary disease

Exclusion Criteria:

  • exacerbation of the pulmonary disease
  • Weight >150Kg
  • Refusal to participate
  • People in pre and post surgical rehabilitation

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03793504


Contacts
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Contact: Marc BEAUMONT, PhD +33298626160 ext 7750 mbeaumont@ch-morlaix.fr
Contact: Marc BEAUMONT, PhD +33298626160 ext 7750 marc.beaumont@chu-brest.fr

Locations
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France
CH Morlaix Recruiting
Morlaix, France, 29672
Contact: Marc BEAUMONT, PhD    +33298626160 ext 7750    mbeaumont@ch-morlaix.fr   
Contact: Marc BEAUMONT, PhD    +33298626160 ext 7750    marc.beaumont@chu-brest.fr   
Sponsors and Collaborators
University Hospital, Brest
Investigators
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Principal Investigator: Marc BEAUMONT, PhD CHRU de Brest

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Responsible Party: University Hospital, Brest
ClinicalTrials.gov Identifier: NCT03793504     History of Changes
Other Study ID Numbers: WIIRR (29BRC18.0250)
First Posted: January 4, 2019    Key Record Dates
Last Update Posted: March 6, 2019
Last Verified: December 2018

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Keywords provided by University Hospital, Brest:
pulmonary rehabilitation
exercise
physical activity
Additional relevant MeSH terms:
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Lung Diseases
Respiratory Tract Diseases