- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04348539
Older People Gait: Physiomechanics and Functionality
April 1, 2021 updated by: Leonardo A. Peyré-Tartaruga, Federal University of Rio Grande do Sul
Evaluation of the Effects of Coordination, Strength and Cardiorespiratory Endurance Training on Physical Fitness, Kinematic and Physiomechanics Parameters of Gait and Indicators Associated With the Quality of Life in Older People
The aim of study is to investigate gait in active elderly people regarding the kinematic parameters of gait, indicators of physical fitness and quality of life.
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Detailed Description
Objective: Evaluate and compare the effects of different types of training (balance training, strength training, cardiorespiratory endurance training); in the older people in the variables of physical fitness (dynamic balance, static balance, rate of strength production, flexibility and cardiorespiratory endurance), physiomechanics of gait (length and frequency of stride, time of contact and balance, energy conversion, mechanical work , transport cost, dynamic stability and mechanical efficiency of walking at different speeds), indicators associated with quality of life (depressive symptoms, health-related quality of life, fear of falling).
Experimental Design: study experimental randomized.
Search Location: Exercise Research Laboratory at the School of Physical Education, Physiotherapy and Dance, Federal University of Rio Grande do Sul, Porto Alegre, Rio Grande do Sul, Brazil.
Participants: older people from the community of both sexes, aged 60 or over, sedentary.
Interventions: In this research, three groups of older people will receive intervention during 4 months of different types of training (balance training, strength training, cardiorespiratory endurance training); and a control group, who will receive educational lectures on health, walking and aging.
The training programs will have a duration of 4 months and will be periodized so that the duration of the sessions is same between them.
The intensity of the interval training will be manipulated by the subjective effort scale (Borg) and by exercise time.
The training programs will have a frequency of two sessions per week and a duration of 45 minutes.
In order to evaluate the effects of the training, evaluations will be performed before and after the training period.
Outcomes: the results will be related to the variables physical fitness, physiomechanics of gait, and indicators associated with quality of live.
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, and Bonferroni post-hoc to identify the differences between the means in all variables.
Expected Results: The investigators believe that the better the level of physical fitness, the less likely it is that the elderly will enter into a frame of disability or fragility, especially improving physical fitness when compared to the control group.
In addition, strategies to protect the elderly can be formulated through physical programs aimed at preventing the functional capacity and quality of life of the elderly.
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.
Study Type
Interventional
Enrollment (Anticipated)
60
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Leonardo Alexandre Peyré-Tartaruga, PhD
- Phone Number: +555133085818
- Email: leonardo.tartaruga@ufrgs.br
Study Locations
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Rio Grande Do Sul
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Porto Alegre, Rio Grande Do Sul, Brazil, 90690200
- Federal University of Rio Grande do Sul
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
60 years to 95 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- volunteers
- aged over 60 years
- both sexes
- not performing regular physical activity with professional monitoring
Exclusion Criteria:
- not participate in all stages of the evaluation
- 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.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Balance training
The balance training consists of 3 moments: warm up, main and stretch.
Warm-up with mobility exercises for major joints and large muscle groups.
The main part will have eight exercise stations divided into: a) five balance exercises (dynamic and static with or without object balance) on a varied floor, b) three agility exercises, and a stretching of the worked muscle groups and a final relaxation.
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32 sessions will be held twice a week, with each session taking an average of 45 minutes
Other Names:
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Experimental: Strength training
Muscle strength training will consist of 3 moments: warm up, main and stretch.
Warm up with mobility exercises for the main joints and large muscle groups.
The main part will include strength exercises with lower and upper limbs with two sets of 6-12 repetitions according to periodization, and a stretching of the muscle groups worked
|
32 sessions will be held twice a week, with each session taking an average of 45 minutes
Other Names:
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Experimental: Cardiorespiratory endurance training
The older people walking training consists of 3 moments: warm up, main and stretch.
They will do a brief free walking warm-up for 3 minutes in the Self-selected walking speed, then walk according to the training cycle, and then a stretching of the main muscle groups.
Will be held, twice a week for 45 minutes each session.
The training intensity will follow 60-110% of the volume of the 6-minute Test (6MWT) and the Borg Scale at moderate to difficult intervals.
the training
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32 sessions will be held twice a week, with each session taking an average of 45 minutes
Other Names:
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No Intervention: Control group
control group: who will receive educational lectures on health, walking and aging.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Dynamic Balance
Time Frame: Change from baseline at 16 weeks
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Dynamic balance: Timed Get Up and Go test (distance of 3 meters), which give the time (seconds) that the individual takes to complete the path of the test as fast as possible (without running).
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Change from baseline at 16 weeks
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Strength
Time Frame: Change from baseline at 16 weeks
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Lower limb strength: Test to get up and sit on the chair.
The individual sits on the chair, with his arms crossed over his chest and at the signal starts the repetitions of getting up and sitting down for a total of 30 seconds.
The number of repetitions the subject is able to perform is added.
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Change from baseline at 16 weeks
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Cardiorespiratory endurance
Time Frame: Change from baseline at 16 weeks
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cardiorespiratory endurance: 6-minute test.
The individual will walk in a 30 meters course for 6 minutes as fast as he can, without running, resulting in the distance covered in that interval.
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Change from baseline at 16 weeks
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Static balance
Time Frame: Change from baseline at 16 weeks
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Static balance: force platform by means of the displacement rate of the centre of mass in the anteroposterior (Fx), medium-lateral (Fy) and vertical (Fz) axes.
The older people must climb on the platform and unite their feet, keeping their gaze in a fixed linear point, the test will last for 30 seconds, it will be registered with the eyes open and closed
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Change from baseline at 16 weeks
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Locomotor Rehabilitation Index
Time Frame: Change from baseline at 16 weeks
|
Locomotor Rehabilitation Index: method of determining how close is the self-selected walking speed compared to the Optimum Speed.
The results is given in percent, and when Locomotor Rehabilitation Index value is closer to 100 percent, it indicates that the participants are closer to their theoretical optimal walking speed.
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Change from baseline at 16 weeks
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Self-selected walking speed
Time Frame: Change from baseline at 16 weeks
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Self-selected walking speed: This outcome will be measure in test of walking treadmill
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Change from baseline at 16 weeks
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Anthropometric data - Body mass
Time Frame: Change from baseline at 16 weeks
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Body mass: measure in kilograms before and after interventions.
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Change from baseline at 16 weeks
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Depressive symptoms
Time Frame: Change from baseline at 16 weeks
|
Geriatric Depression Scale protocol: consists of 15 questions in which participants are asked to answer yes or no in reference to how they felt over the past week (for instance, "Do the patient feel that their life is empty?,"
Do the patient feel that their situation is hopeless?).
Scores range from 0 to 15 with higher scores indicating more depressive symptoms.
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Change from baseline at 16 weeks
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Health-related quality of life: Medical Outcomes Study 36 - Item Short Form Health Survey
Time Frame: Change from baseline at 16 weeks
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Medical Outcomes Study 36 - Item Short Form Health Survey: multidimensional questionnaire, formed by 36 items that encompass eight domains (functional capacity, physical aspects, pain, general health status, vitality, social aspects, emotional aspects and mental health).
The maximum score for each domain is 100, with the total sum being a maximum of 150, with zero being "worst" and 150 "best health status".
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Change from baseline at 16 weeks
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Fear of falling
Time Frame: Change from baseline at 16 weeks
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Falls Efficacy Scale - International: questions about the concern with the possibility of falling when performing 16 activities, with respective scores from one to four.
The total score can vary from 16 (no concern) to 64 (extreme concern).
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Change from baseline at 16 weeks
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Anthropometric data - Height
Time Frame: Change from baseline at 16 weeks
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Height: measure in meters before and after interventions.
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Change from baseline at 16 weeks
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Anthropometric data - Body Mass Index
Time Frame: Change from baseline at 16 weeks
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Body Mass Index: Weight and height will be combined to report the body mass index in kg/m2.
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Change from baseline at 16 weeks
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Spatial Parameter - Stride length
Time Frame: Change from baseline at 16 weeks
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This outcome is measure by stride length in meters.
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Change from baseline at 16 weeks
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Temporal Parameter - Swing time, contact time, time of balance
Time Frame: Change from baseline at 16 weeks
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Swing time in seconds, contact time in seconds, time of balance in seconds.
The percentage of contact time will be calculated to measure the duty factor in percentual.
The swing and contact time in seconds will be aggregated to distance in meters to arrive at frequency (in Hetz).
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Change from baseline at 16 weeks
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Parameters of Pendular Mechanism - Internal Work
Time Frame: Change from baseline at 16 weeks
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The transduction between the potential and kinetic mechanical energies of the center of body mass (called the "inverted pendulum" mechanism).
The internal work is the mechanical energy fluctuations of the movement of limbs relative to the center of body mass (Wint, in Joules).
This outcome will be measured through the registered image movement analysis using the three-dimensional motion analysis system VICON of the walking test on the treadmill.
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Change from baseline at 16 weeks
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Parameters of Pendular Mechanism - external work
Time Frame: Change from baseline at 16 weeks
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The transduction between the potential and kinetic mechanical energies of the center of body mass (called the "inverted pendulum" mechanism).
The external work is energy fluctuations of the center of body mass with respect to the external environment or surroundings (Wext, in Joules).
This outcome will be measured through the registered image movement analysis using the three-dimensional motion analysis system VICON of the walking test on the treadmill.
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Change from baseline at 16 weeks
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Parameters of Pendular Mechanism: total mechanical work
Time Frame: Change from baseline at 16 weeks
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The transduction between the potential and kinetic mechanical energies of the center of body mass (called the "inverted pendulum" mechanism).
The total mechanical work (Wtot =internal Work + External Work) produced by a body during activity.
These outcomes are measured by composite for:(external, internal mechanical work, in Joules).
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Change from baseline at 16 weeks
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Parameters of Pendular Mechanism: Recovery
Time Frame: Change from baseline at 16 weeks
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The mechanical energy exchange of the center of mass is quantified by the calculation of the percentage of reconversion of mechanical energy, called Recovery (R), which counts the form that the mechanical energy is saved through the pendulum mechanism of the locomotion.
This outcome will be measured through the registered image movement analysis using the three-dimensional motion analysis system VICON of the walking test on the treadmill.
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Change from baseline at 16 weeks
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Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Sociodemographic characteristics
Time Frame: Change from baseline at 16 weeks
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Anamnesis with basic information about age, sex, marital status, education, occupation, housing, occurrence of diseases, use of medication.
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Change from baseline at 16 weeks
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Cognitive function
Time Frame: Change from baseline at 16 weeks
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Montreal Cognitive Assessment (MoCA), Portuguese version, evaluates 8 domains of cognitive functioning: attention and concentration, executive functions, memory, language, visuoconstructive abilities, conceptual thinking, calculations and guidance.
The total score is 30 points; a value = 26 is considered normal.
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Change from baseline at 16 weeks
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Lower limb flexibility
Time Frame: Change from baseline at 16 weeks
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Lower limb flexibility: sit and reach test.
The individual sits in the chair with his leg extended, slowly leans forward, trying to touch his toes.
A measurement is made from the toes to the fingertips.
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Change from baseline at 16 weeks
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Study Director: Leonardo Alexandre Peyré-Tartaruga, PhD, Federal University of Rio Grande do Sul
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- GONÇALVES, A. K.; et al. Postural balance program: variables related to falls in elderly. Journal of Physical Education, v. 28, 2017
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Anticipated)
May 1, 2021
Primary Completion (Anticipated)
December 1, 2021
Study Completion (Anticipated)
March 1, 2022
Study Registration Dates
First Submitted
March 25, 2020
First Submitted That Met QC Criteria
April 14, 2020
First Posted (Actual)
April 16, 2020
Study Record Updates
Last Update Posted (Actual)
April 2, 2021
Last Update Submitted That Met QC Criteria
April 1, 2021
Last Verified
April 1, 2021
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- GaitOlderpeople
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
No
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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