Fondation Saint Helier
Rennes, 35043, France
Location status: Recruiting
NCT Number: NCT07230002
While clinical assessment of locomotor function in this population is carried out using tasks involving walking in a straight line without any obstacles, it does not take into account ecological situations (i.e., situations comparable to real-life situations) in which the person interacts with their environment, such as walking down a street with other pedestrians, which is fundamental to everyday life. This research therefore aims to study the social navigation skills during locomotion of people who have suffered a moderate or severe head injury in the chronic phase in more ecological tasks. This will provide a better understanding of the difficulties encountered by these patients during locomotor interactions in everyday life.
Interested in participating?
Request Info18 year–55 year
All sexes
Interventional
Not applicable
Rennes, 35043, France
Location status: Recruiting
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
for Traumatic Brain Injury group :
Inclusion criteria
for healthy control group :
Exclusion criteria
specific to patients in the traumatic brain injury group :
Exclusion criteria
for both groups :
Exclusion criteria
for healthy control group :
Patients and participants will be asked to perform several walking/locomotion tasks in a virtual evironment setting. The setting in question is a concert in a parc. The participants will have to walk towards the stage whilst avoiding bumping into "virtual people". A total of 5 different tasks (walking in a straight line, walking between people etc) will be completed for each participant. Different variables will then be recorded and extracted such as walking speed, interpersonnal distances, eye fixation times.
Time frame: From enrollment to the end of the participation at maximum 30 days
Time frame: From enrollment to the end of the participation at maximum 30 days
Time frame: From enrollment to the end of the participation at maximum 30 days
Time frame: From enrollment to the end of the participation at maximum 30 days
Time frame: From enrollment to the end of the participation at maximum 30 days
Time frame: From enrollment to the end of the participation at maximum 30 days
Time frame: On day 1
Time frame: At day 1
Time frame: At day 1
Time frame: At day 1
Time frame: At day 1
Contact information is provided by the study sponsor or research team.
Pôle Saint Hélier
Other
Acronym: NAVIGO
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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