Comparison of Training in Virtual Environment With and Without Physiotherapeutic Intervention in Chronic Stroke Patients

Sponsor
University of Sao Paulo General Hospital (Other)
Overall Status
Completed
CT.gov ID
NCT03361241
Collaborator
(none)
40
1
2
32.9
1.2

Study Details

Study Description

Brief Summary

The aim of this study is to compare the effects of balance training in a virtual environment with and without physiotherapeutic intervention on the motor function, balance and gait in chronic stroke patients.

It is a prospective, single blinded, randomized clinical trial performed at Center of Research of the Department of Speech Therapy, Physical Therapy and Occupational Therapy of São Paulo University. Forty patients will be randomly assigned in control and experimental group.

Condition or Disease Intervention/Treatment Phase
  • Other: No Physiotherapeutic Intervention
  • Other: Physiotherapeutic Intervention
N/A

Detailed Description

The aim of this study is to compare the effects of a balance training program in a virtual environment (using a gaming system with balance board device) with and without verbal/manual physiotherapeutic intervention, on the motor function, balance and gait in chronic stroke patients.

It is a prospective, single blinded, randomized clinical trial, performed at Center of Research of the Department of Speech Therapy, Physical Therapy and Occupational Therapy of São Paulo University.

Forty chronic stroke patients will be randomly in control and experimental group, 20 each one. Both groups conduct 14 training sessions, twice a week, for seven weeks. Each session will consist a 30 minute-global-exercise series including stretching, muscle strength and axial mobility exercises. After this, both groups will perform more 30 minutes of balance training using eight Wii Fit games which stimulate motor and cognitive functions.

The main outcome measures will be: the lower limb subscale of the Fugl-Meyer Assessment (FMA-LE); Balance Evaluation Systems Test (BESTest) and 6- minute walk test (6MWT).

Study Design

Study Type:
Interventional
Actual Enrollment :
40 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Parallel AssignmentParallel Assignment
Masking:
Single (Outcomes Assessor)
Masking Description:
Single blinded (outcomes assessor)
Primary Purpose:
Treatment
Official Title:
Comparison of Effects of Training in a Virtual Environment With and Without Physiotherapeutic Intervention on the Motor Function, Postural Control and Gait in Chronic Stroke Patients : A Randomized Controlled Trial
Actual Study Start Date :
Apr 2, 2017
Actual Primary Completion Date :
Nov 30, 2018
Actual Study Completion Date :
Dec 30, 2019

Arms and Interventions

Arm Intervention/Treatment
Experimental: No Physiotherapeutic Intervention

Virtual reality training without physiotherapeutic intervention

Other: No Physiotherapeutic Intervention
Experimental group will perform a balance training program in a virtual environment (using a gaming system with balance board device - eight games of Nintendo Wii Fit®, for 14 sessions) without verbal/manual physiotherapeutic intervention. Initially, instructions about the rules and strategies of how to play the game and control the avatar will be provided. Then the patient will be invited to start the game, and in the two attempts of the training no manual or verbal assistance will be provided. Physiotherapist participation during training will be restricted to ensuring patient safety, providing motivational verbal stimuli, and replicating the feedback provided by the game at the end of each attempt.
Other Names:
  • Experimental Group
  • Active Comparator: Physiotherapeutic Intervention

    Virtual reality training with physiotherapeutic intervention

    Other: Physiotherapeutic Intervention
    Control group will perform a balance training program in a virtual environment (gaming system with balance board device - eight games of Nintendo Wii Fit®, for 14 sessions) with verbal and manual physiotherapeutic intervention. Initially, instructions about the rules and strategies of how to play the game and control the avatar will be provided. Then the patient will be invited to start the game, and in the first attempt of the training physiotherapist will provide manual and verbal assistance, providing corrections on movement (avoiding compensatory movements). In the second attempt, no manual or verbal assistance will be provided (only ensuring patient safety, providing motivational verbal stimuli), allowing the patient to organize his or her performance.
    Other Names:
  • Control Group
  • Outcome Measures

    Primary Outcome Measures

    1. Balance Evaluation Systems Test (BESTest) [Up to 3 months]

      Balance Evaluation Systems Test (BESTest) measures balance. It includes 36 items that evaluate performance of 6 balance systems: biomechanical constraints, stability limits/verticality, anticipatory postural adjustments, postural responses, sensory orientation, and stability in gait.

    Secondary Outcome Measures

    1. The lower limb subscale of the Fugl-Meyer Assessment (FMA-LE) [Up to 3 months]

      FMA-LE is a subscale measuring lower limb motor recovery. It examines movement and coordination of the hip, knee, and ankle in the supine, sitting, and standing positions. Each item is scored on a 3-point scale (0, cannot perform; 1, partially performs; 2, performs fully). The score range is 0 to 34, with higher scores indicating better lower limb motor performance

    2. 6-minute walk test [Up to three months]

      The 6MWT is a practical simple test. This test measures the distance that a patient can quickly walk on a flat, hard surface in a period of 6 minutes (the 6MWD). The 6MWT has been used as a measure of functional status of patients.

    3. Limits of Stability [Up to 3 months]

      The Limits of Stability subtest quantifies the maximum distance a person can intentionally displace their center of pressure (COP) from start position of midline COP centered over the base of support to eight targets. Location and movement of the COP was indicated by a cursor display projected on a screen in front of the subject. As targets were highlighted, the subject was to move the COP cursor quickly and accurately as possible towards a target located on the Limits of Stability perimeter and hold position as close to the target as possible. The parameters include COP movement velocity and directional control (% to target).

    4. Rhythmic Weight Shift [Up to three months]

      The Rhythmic Weight Shift quantifies the subject's active weight shift ability by moving the COP cursor to match velocity and direction of a moving visual target in the medial- lateral (ML) and anterior-posterior (AP) directions at three different velocities.

    5. Stroke Specific quality of life scale [Up to three months]

      Stroke Quality of Life Scale is a self-report assessment that includes 12 stroke subscales with 49 items. The Stroke Specific Quality of Life Scale attempts to capture the domains of stroke QOL that are insufficiently assessed with generic QOL measures. The 12 subscales, which are unidimensional, are Energy, Family Role, Language, Mobility, Mood, Personality, Self-Care, Social Roles, Thinking, Upper Extremity Function, Vision, and Work-Productivity. Participants responded to each item on a 5-point scale. Domain scores are the averages of the item scores, and the total score is the average of the domain scores. All summary scores therefore range from 1 to 5. Higher scores indicate better function.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 65 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • hemiparetic status resulting from a single stroke at least 6 months earlier;

    • the ability to walk 10 m independently with or without an assistive device;

    • a Montreal Cognitive Assessment (MoCA) score of ≥ 20;

    • the absence of a musculoskeletal condition that could potentially affect the ability to stand or walk safely;

    • the absence of serious visual impairment or a hearing disorder;

    • muscle strength ≥ 3 in lower limbs;

    • ability to understand and follow simple instructions.

    Exclusion Criteria:
    • severe dementia or aphasia;

    • hemispatial neglect, ataxia or any other cerebellar symptom;

    • inability to stand without minimal assist;

    • uncontrollable medical complications

    • participation in other studies or rehabilitation programs

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Department of Physiotherapy, Communication Science & Disorders, Occupational Therapy, School of Medicine, University of São Paulo Sao Paulo SP Brazil 05360-160

    Sponsors and Collaborators

    • University of Sao Paulo General Hospital

    Investigators

    • Study Director: Maria Elisa P Piemonte, PT, PhD, University of São Paulo
    • Principal Investigator: Mariana A Lourenço, PT,Ms Student, University of São Paulo
    • Principal Investigator: Tatiana P Oliveira, PT,PhD Student, University of São Paulo
    • Principal Investigator: Camila S Miranda, PT, MS, University of São Paulo

    Study Documents (Full-Text)

    More Information

    Publications

    Responsible Party:
    University of Sao Paulo General Hospital
    ClinicalTrials.gov Identifier:
    NCT03361241
    Other Study ID Numbers:
    • USPCR001
    First Posted:
    Dec 4, 2017
    Last Update Posted:
    Feb 18, 2020
    Last Verified:
    Aug 1, 2019
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by University of Sao Paulo General Hospital
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Feb 18, 2020