Gait Re-education Program in Subjects With Parkinson´s Disease

Sponsor
Universidad Europea de Madrid
Study ID
NCT05131880
Status
Completed

Conditions

Eligibility Criteria

Sex
ALL
Age
50 Years - 100 Years
Healthy Volunteers
Not accepted

Interventions

  • Gait Re-education Program Using the Fisior® Mat Sequential Training System in Subjects with Parkinson's Disease — OTHER
    Randomized controlled study that will include participants diagnosed with Parkinson's disease in mild or moderate stage with altered gait pattern who will be randomized following a simple randomization procedure in which one group will perform an intervention based on a gait re-education program called "TAPIZ FISIOR®"- motor control and learning added to a conventional physiotherapy program; and the other group will perform only a conventional physiotherapy program. The evaluators will be unaware of the patient's treatment condition.

Study Details

Randomized controlled study that will include participants diagnosed with Parkinson's disease in mild or moderate stage with altered gait pattern who will be randomized following a simple randomization procedure in which one group will perform an intervention based on a gait re-education program called "TAPIZ FISIOR"- motor control and learning added to a conventional physiotherapy program; and the other group will perform only a conventional physiotherapy program. The evaluators will be unaware of the patient's treatment status.

Key Dates

Start date
Nov 1, 2021
Status verified
Sep 2025
Primary completion
Apr 1, 2022
Completion
May 1, 2024

Study Design

Enrollment
52 participants (actual)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT

Arms

  • Experimental: 'TAPIZ FISIOR' gait re-education program combined with conventional physiotherapy program.
    The experimental group will undergo a physiotherapy program supplemented by the Fisior Mat Method, with three sessions per week over a 12-week period. Assessments will be conducted at baseline, immediately after the intervention, and at follow-up.
  • Active Comparator: Conventional physiotherapy program
    The control group will participate in a physiotherapy program three sessions per week for 12 weeks.

Primary Outcome Measure

Physical Performance: The Short Physical Performance Battery (SPPB) [ Time Frame: Before the intervention, up to 15 minutes; and at the end of 12 weeks intervention, up to 15 minutes. ]

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