Healthy Clinical Trial
— MoveNIRSOfficial title:
Effect of Rhythmic Auditory Stimulation (RAS) During Gait on Cortical Activation: A Functional Near-infrared Red Spectroscopy Neuroimaging Study (fNIRS)
NCT number | NCT05789121 |
Other study ID # | CHRO-2022-09 |
Secondary ID | |
Status | Completed |
Phase | |
First received | |
Last updated | |
Start date | March 14, 2023 |
Est. completion date | March 24, 2023 |
Verified date | March 2023 |
Source | Centre Hospitalier Régional d'Orléans |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
The purpose of this study is to investigate the cerebral activation in healthy subjects in 4 conditions of gait : - Gait at preferred cadence without auditory stimulation (Gait1) - Gait with low tempo rhythmic auditory stimulation by music (RAS-Slow). The beat rate of the music was 68.5 per minute for all participants. - Gait with fast tempo synchronous rhythmic auditory stimulation by music (RAS-Fast). The beat rate of the music was set to 10% above each patient's preferred gait cadence . The preferred cadence was considered as the mean of the 6 trials during Gait 1. - Gait without auditory stimulation (Gait2) The investigators goal is to compare cerebral activation and gait parameters during the 4 different tasks using fNIRS.
Status | Completed |
Enrollment | 29 |
Est. completion date | March 24, 2023 |
Est. primary completion date | March 24, 2023 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 40 Years |
Eligibility | Inclusion Criteria: - Age 18 to 40 years old. - No known neurological disease - Benefiting from a social security coverage. - Sufficient knowledge of the French language to understand the instructions Exclusion Criteria: - Person under tutorship or curatorship - Known allergy to components of the fNIRS device: neoprene - History of neurological disease - History of rheumatological disease affecting walking - Pregnant or breastfeeding women - Subjects opposed to participating in the study |
Country | Name | City | State |
---|---|---|---|
France | CHR Orléans | Orléans |
Lead Sponsor | Collaborator |
---|---|
Centre Hospitalier Régional d'Orléans |
France,
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Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Mean change in the concentration of oxyhemoglobin during the task | Day 0 | ||
Primary | Mean change in the concentration of deoxyhemoglobin during the task | Day 0 | ||
Secondary | Walking speed | Day 0 | ||
Secondary | Number of steps within a minute walk (in steps/min) | Number of steps within a minute walk (in steps/min) | Day 0 | |
Secondary | stride length | Day 0 | ||
Secondary | double support time | Day 0 |
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