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Clinical Trials/NCT03919968
NCT03919968CompletedNot Applicable

Effect of Muay Thai vs. Circuit Training on the Health of Elderly: A Randomized Clinical Trial

Universidade Estadual Paulista Júlio de Mesquita Filho1 site in 1 country36 target enrollmentStarted: February 1, 2019Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
36
Locations
1
Primary Endpoint
Autonomic Cardiac Modulation

Study Overview

Brief Summary

The elderly will be recruited, after meeting the inclusion criteria, will be submitted to data collection, all necessary assessments for the study and after 12 weeks, the same data will be collected, so that the elderly are self-control. After the second collection, the elderly will be randomized into two groups: the Muay Thai group and the functional training group. Both groups will train three times a week for 60 min and for 12 weeks. The training will be divided into 20 min of general exercises, 20 min of specific exercises and 20 min of fight simulation and/or play activities. At the end of the 12 weeks of intervention, evaluations and data collection will be performed again.

Detailed Description

Will be recruited through media resources at least 50 elderly people aged between 60 and 89 years.

Inclusion Criteria:

Being literate; Age between 60 and 89 years; Ability to perform moderate-intensity exercises determined by the American College Sports Medicine (ACSM) assessment questionnaire; Medical certificate stating that the elderly are able to exercise; Sign the informed consent form.

Exclusion Criteria:

Perform any other systematic practice of physical exercise, in addition to regular physical activity, such as walking; Present serious cardiovascular pathologies; Present serious neurological pathologies; Present use of crutches, walking sticks, walkers, wheelchairs or other similar utensils; Present self-report of locomotion difficulties to carry out the intervention practice.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Prevention
Masking
Single (Outcomes Assessor)

Eligibility Criteria

Ages
60 Years to 89 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •Being literate;
  • •Age between 60 and 89 years;
  • •Ability to perform moderate-intensity exercises determined by the American College Sports Medicine (ACSM) assessment questionnaire;
  • •Medical certificate stating that the elderly are able to exercise;
  • •Sign the informed consent form.

Exclusion Criteria

  • •Perform any other systematic practice of physical exercise, in addition to regular physical activity, such as walking;
  • •Present serious cardiovascular pathologies;
  • •Present serious neurological pathologies;
  • •Present use of crutches, walking sticks, walkers, wheelchairs or other similar utensils;
  • •Present self-report of locomotion difficulties to carry out the intervention practice.

Arms & Interventions

Martial Arts

Experimental

The training will be performed 3 times a week, for 12 weeks, during 60 minutes, being that will be divided into 20 min of general exercises, 20 min of specific exercises and 20 min of fight simulation and / or play activities. The activities will be carried out in a way adapted for the elderly. Will be used kickers, gauntlets, thorax and head protectors, shin guards, gloves, and other devices.

Intervention: Functional Training (Behavioral)

Functional Training

Active Comparator

The training will be performed 3 times a week, for 12 weeks, during 60 minutes, being that will be divided into 20 min of general exercises, 20 min of specific exercises and 20 min of play activities. The activities will be carried out in a way adapted for the elderly. Will be carried out neuromotor control / coordination, balance, flexibility and static and dynamic stabilization. They will also have acceleration and deceleration activities, rotation and counter-rotation, extension and counter-extension, flexion and counter-flexion.

Intervention: Martial Arts (Behavioral)

Outcomes

Primary Outcomes

Autonomic Cardiac Modulation

Time Frame: Change from Baseline Autonomic Cardiac Modulation to 3 months after intervention

The heart rate variability will be collected by means of the POLAR V800.

Secondary Outcomes

  • Muscle mass(Pre baseline, Post 3 months (Pre-intervention) and Post 6 months (Post-intervention))
  • Systolic Blood pressure(Pre baseline, Post 3 months (Pre-intervention) and Post 6 months (Post-intervention))
  • Self-reported physical activity level questionnaire(Pre baseline, Post 3 months (Pre-intervention) and Post 6 months (Post-intervention))
  • Quality of life questionnaire(Pre baseline, Post 3 months (Pre-intervention) and Post 6 months (Post-intervention))
  • Cardiorespiratory capacity- 6-minute walk test(Pre baseline, Post 3 months (Pre-intervention) and Post 6 months (Post-intervention))
  • Fat mass(Pre baseline, Post 3 months (Pre-intervention) and Post 6 months (Post-intervention))
  • Resting heart rate(Pre baseline, Post 3 months (Pre-intervention) and Post 6 months (Post-intervention))
  • Physical activity level - objective measure(Pre baseline, Post 3 months (Pre-intervention) and Post 6 months (Post-intervention))
  • Force- objective measure(Pre baseline, Post 3 months (Pre-intervention), Post-intervention 6 months)
  • Body fat(Pre baseline, Post 3 months (Pre-intervention) and Post 6 months (Post-intervention))
  • Self-reported sedentary behaviour questionnaire(Pre baseline, Post 3 months (Pre-intervention) and Post 6 months (Post-intervention))
  • Agility and dynamic balance - objective measure(Pre baseline, Post 3 months (Pre-intervention) and Post 6 months (Post-intervention))
  • Bone Mineral Density(Pre baseline, Post 3 months (Pre-intervention) and Post 6 months (Post-intervention))
  • Diastolic Blood pressure(Pre baseline, Post 3 months (Pre-intervention) and Post 6 months (Post-intervention))
  • Blood flow of the arteries(Pre baseline, Post 3 months (Pre-intervention) and Post 6 months (Post-intervention))
  • Flexibility- objective measure(Pre baseline, Post 3 months (Pre-intervention) and Post 6 months (Post-intervention))
  • Cognitive ability(Pre baseline, Post 3 months (Pre-intervention) and Post 6 months (Post-intervention))
  • Flow-mediated dilation(Pre baseline, Post 3 months (Pre-intervention) and Post 6 months (Post-intervention))
  • Thickness of the arteries(Pre baseline, Post 3 months (Pre-intervention) and Post 6 months (Post-intervention))
  • Anxiety and depression questionnaire(Pre baseline, Post 3 months (Pre-intervention) and Post 6 months (Post-intervention))

Investigators

Sponsor
Universidade Estadual Paulista Júlio de Mesquita Filho
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Bruna Thamyres Ciccotti Saraiva

Principal Investigator

Universidade Estadual Paulista Júlio de Mesquita Filho

Study Sites (1)

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