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Supraspinal Contributions to the Control of Human Locomotion: Clinical and Fundamental Aspects

Supraspinal Contributions to the Control of Human Locomotion: Clinical and Fundamental Aspects

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02263560
Acronym
SUPLOCO
Enrollment
20
Registered
2014-10-13
Start date
2014-03-31
Completion date
2016-03-31
Last updated
2017-10-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Post-stroke Gait Assessments

Brief summary

Many neurological patients express enhanced deficits while walking in a dark room (or during the night): the supraspinal structures involved in this navigational deficit have not been identified yet. In this project, the investigators will study post-stroke gaits of human patients and compare them to those of a control population during a goal-oriented task performed in different visual conditions. The investigators want to test the hypothesis that during simple goal-oriented locomotor tasks, only patients with specific (e.g. medio or infero- temporal) lesions will express navigational deficits.

Interventions

BEHAVIORALKinematic measurements

Sponsors

Dr Titus Bihl, Hopital Cantonal Fribourgeois
CollaboratorUNKNOWN
University of Fribourg
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
OTHER

Eligibility

Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
Yes

Inclusion criteria

(for matching controls): * Adult male and female subjects (18--\>85 years old)

Exclusion criteria

(for matching controls): * Persons with history of an acquired or congenital neurological disorder, e.g. stroke, multiple sclerosis, Parkinson disease, increased intracranial pressure, etc.; * Persons injured at the time of the experiments (fractures,…); * Persons having reported repetitive spatial troubles/disorders; * Persons with eye disorders and non-corrected vision problems; * Pregnant women.

Design outcomes

Primary

MeasureTime frame
Walking stability indices of post-stroke patients1 hour and 30 minutes (including pre-tests, instructions delivery...).
Spatial accuracy of walking trajectories in post-stroke patients1 hour and 30 minutes (including pre-tests, instructions delivery...).

Countries

Switzerland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026