- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02516189
Strength Training for Elderlies and Their Effects on Muscle Fatigue and Microcirculation - Randomized Clinical Trial
Study Overview
Detailed Description
Purpose
The primary research question is:
Do muscular strength training programs can improve functional capacity, muscle performance and microcirculation in the elderly? Hypothesis: Strength training program will promote electromyographic changes during the development of peripheral muscle fatigue and microcirculatory blood flow contributing to functional autonomy.
Secondary Research Questions
- Does the strength training program in the elderly improve the standard of electromyographic fatigue? Hypothesis: Elderly practitioners of strength exercise program showed increased neuromuscular efficiency and electromyographic fatigue index.
- Do the strength training program in the elderly improve peripheral microcirculation? Hypothesis: A regular program of strength exercise in the elderly increases the blood flow in peripheral microcirculation changing the process of muscle fatigue. These biomechanical and physiological changes contribute to increased functional autonomy and reducing the risk of falls in the elderly.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- sedentary elderly
- individuals who have physical and medical conditions to perform strength training
- individuals who participate in the Open University Maturity Program
Exclusion Criteria:
- individuals who do not have physical and medical conditions to perform strength training
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Group A
group of elderly participants of strength training program
|
Strength Training program applied twice a week for sixteen weeks. Each training exercises has a total time of 50 minutes. Warm-up: 5 minutes of stretching. Training: Leg press; Leg Curl; Vertical traction; Chest press; Abdominal crunch; Lower back. Gametherapy. Relaxation: 5 minutes of stretching. |
No Intervention: Group B
group of seniors who did not practice strength training program
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change in elderlies's microcirculatory blood flow after 4 months
Time Frame: 4 months
|
The blood flow in the microcirculation in the elderly will be measured by laser-doppler flowmetry.
The measures blood flow in the microcirculation will be quantified by the reactive hyperemia Post-occlusion protocol (PORH).
|
4 months
|
Change in elderlies's muscle fatigue after 4 months
Time Frame: 4 months
|
muscle fatigue will be quantified by surface electromyography of the muscles of the lower limbs.
The electromyographic fatigue threshold and fatigue index will be calculated by the Root Mean Square (RMS) and Median Frequency variables after 4 months.
|
4 months
|
Change in elderlies's functional capacity after 4 months
Time Frame: 4 months
|
The functional capacity of the elderly will be evaluated by the Berg Balance Scale, the Timed up-and-go Test, and Falls Efficacy Scale International (FES-I) after 4 months
|
4 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change in elderlies's strength after 4 months
Time Frame: 4 months
|
The lower body strength of the elderly will be measured by 30-s chair test stand after 4 months.
|
4 months
|
Change in elderlies's functional autonomy after 4 months
Time Frame: 4 months
|
The functional autonomy of the elderly will be determined by the general functionality index of the Latin American Development Group to Maturity Protocol after 4 months.
|
4 months
|
Collaborators and Investigators
Collaborators
Investigators
- Principal Investigator: Danilo A Vasconcelos, MS, Universidade Estadual da Paraiba
- Principal Investigator: João G Alves, PhD, Instituto de Medicina Integral Professor Fernando Figueira
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- FEFMM
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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