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Gait analysis in patients with Parkinson's Disease before and after a training program in a real and virtual environment

Three-dimensional gait analysis in patients with Parkinson's Disease before and after a training program in a real and virtual environment

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-7pcn85
Enrollment
Unknown
Registered
2018-05-22
Start date
2015-01-01
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

Parkinson's disease

Interventions

They are recruited 30 patients with Parkinson's disease to physical therapy. For the evaluations, individuals will be scheduled in advance in a single session for analysis of walking and rating scales
Other
E01.370.600.250
F04.754.137.506.662

Sponsors

Hospital das Clínicas da Faculdade de Medicina da USP
Lead Sponsor
Hospital das Clínicas da Faculdade de Medicina da USP
Collaborator

Eligibility

Age
60 Years to 80 Years

Inclusion criteria

Inclusion criteria: Patients diagnosed with Parkinson's disease; Age 60-80 years; Patients able to walk more than 10 feet in a straight line; Patients treated with medication; Visual and auditory acuity good.

Exclusion criteria

Exclusion criteria: Volunteers with previous orthopedic surgeries; with other neurological diseases; diabetes mellitus uncontrolled; hypertension uncontrolled; uncontrolled heart disease.

Design outcomes

Primary

MeasureTime frame
Improvement of gait speed (m / s) and length of steps (cm / s) measured by kinematic gait analysis (three-dimensional gait analysis) after conducting treadmill training sessions using virtual reality individuals with Parkinson's disease.

Secondary

MeasureTime frame
Outcomes are not expected secondary.

Countries

Brazil

Contacts

Public ContactJulia Greve

Instituto de Ortopedia e Traumatologia da Faculdade de Medicina da Universidade de São Paulo (FMUSP)

jgreve@usp.br+55-011-26616041

Outcome results

None listed

Source: REBEC (via WHO ICTRP)