Cardio-Respiratory Response of a Training Session Versus an Adapted Physical Activity Session (WIIRR)
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The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. |
| ClinicalTrials.gov Identifier: NCT03793504 |
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Recruitment Status :
Completed
First Posted : January 4, 2019
Last Update Posted : July 16, 2020
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| Condition or disease |
|---|
| Pulmonary Disease |
| Study Type : | Observational |
| Actual 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 |
| Actual Primary Completion Date : | June 17, 2019 |
| Actual Study Completion Date : | June 17, 2019 |
- 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
- 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
- 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
- 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
- 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
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.
| Ages Eligible for Study: | 18 Years and older (Adult, Older Adult) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | No |
| Sampling Method: | Probability Sample |
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
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
| France | |
| CH Morlaix | |
| Morlaix, France, 29672 | |
| Principal Investigator: | Marc BEAUMONT, PhD | CHRU de Brest |
| Responsible Party: | University Hospital, Brest |
| ClinicalTrials.gov Identifier: | NCT03793504 |
| Other Study ID Numbers: |
WIIRR (29BRC18.0250) |
| First Posted: | January 4, 2019 Key Record Dates |
| Last Update Posted: | July 16, 2020 |
| Last Verified: | July 2020 |
| Studies a U.S. FDA-regulated Drug Product: | No |
| Studies a U.S. FDA-regulated Device Product: | No |
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pulmonary rehabilitation exercise physical activity |
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Lung Diseases Respiratory Tract Diseases |

