MUSCLE - Nordic and Free Walking in People With Multiple Sclerosis: Clinical-functional, Motor Control, and Gait Analysis Findings: a Randomized Controlled Multicentre Clinical Trials
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Multiple Sclerosis, Chronic Progressive
- Sponsor
- Leonardo A. Peyré-Tartaruga
- Enrollment
- 60
- Locations
- 1
- Primary Endpoint
- Locomotor Rehabilitation Index
- Status
- Not yet recruiting
- Last Updated
- 3 years ago
Overview
Brief Summary
The aim of the study is to analyze the effects of Nordic Walking and free walking in the clinical-functional, postural balance, motor control, muscular echographic quality, and gait analysis (pendulum gait mechanism), in people with Multiple Sclerosis.
Detailed Description
Objective: Analyze the effects of Nordic Walking and free walking in the clinical-functional parameters, postural balance, muscular echography quality, pendulum gait mechanism, in people with Multiple sclerosis. Experimental Design: Randomized controlled multicenter clinical trial with translational study characteristics. Search Location: Exercise Research Laboratory at the School of Physical Education, Physiotherapy and Dance, Federal University of Rio Grande do Sul, Brazil, and University of Pavia, on Department of Public Health, Experimental Medicine and Forensic Sciences, Pavia, Italy. Participants: 60 patients from the Unified Health System (UHS) of both sexes, from 20 to 75 years old, diagnosed with multiple sclerosis, sedentary. Interventions: In this research, four groups of patients with multiple sclerosis will receive intervention during 4 months of different physical therapy programs (Nordic walking and free walking), who will receive telephone guidance for performing home-based exercises. The training programs will have a duration of 3 months and will be periodized so that the duration of the sessions is matched between them. The intensity of the interval training will be manipulated by the subjective effort scale (Borg) and by the heart rate, with predetermined series durations. All training programs will have a frequency of two sessions per week and a duration of 60 minutes. To evaluate the effects of the training, evaluations will be performed before and after the training period: 1) Basal (month 0): initial pre-training evaluation; 2) month 4: Evaluation 48h after the last training session. Outcomes: clinical-functional parameters, postural balance, muscular echography quality, pendulum gait mechanism, and biochemistry. Data Analysis: Data will be described by average values and standard deviation values. The comparisons between and within groups will be performed using a Generalized Estimating Equations (GEE) analysis, adopting a level of significance (α) of 0.05. Expected Results: The intervention groups of the Nordic walking are expected to be more effective in all outcomes analyzed, especially improving functional mobility when compared to the control group of unsupervised home exercises. In addition, it is expected that the results of the research will be expandable and the possibility of future developments in the scientific, technological, economic, social, and environmental fields and that they will be implemented in the Unified Health System (UHS).
Investigators
Leonardo A. Peyré-Tartaruga
Associate Professor
Federal University of Rio Grande do Sul
Eligibility Criteria
Inclusion Criteria
- •volunteers aged over 20 years;
- •of both sexes;
- •with a clinical diagnosis of multiple sclerosis.
Exclusion Criteria
- •severe heart diseases, uncontrolled hypertension, myocardial infarction within a period of less than one year, being a pacemaker;
- •stroke or other associated neurological diseases; insanity;
- •prostheses in the lower limbs;
- •without ambulation conditions.
Outcomes
Primary Outcomes
Locomotor Rehabilitation Index
Time Frame: Change from baseline at 12 weeks
The Locomotor Rehabilitation Index is a method of determining how close is the SSW compared to the Optimum Speed (Vopt).
Self-selected walking speed
Time Frame: Change from baseline at 12 weeks
SSWS This outcome will be measure in test of treadmill walking
Test Timed Up and Go
Time Frame: Change from baseline at 12 weeks
Test Timed Up and Go: This test evaluates the mobility functional in three meters of self-selected speed (TUGSS) or at forced speed (TUGFS) \[Time Frame: Change from baseline at 12 weeks\]
Secondary Outcomes
- Depressive symptoms(Change from baseline at 12 weeks)
- Quality of life (QoL)(Change from baseline at 12 weeks)
- Optimal Walking Speed (OPT)(Change from baseline at 12 weeks)
- Cognitive function(Change from baseline at 12 weeks)
- Expanded Disability Status Scale(Change from baseline at 12 weeks)