Water Intake Associated With Aerobic Exercise in Coronary

NCT ID: NCT03198806

Last Updated: 2020-07-28

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

31 participants

Study Classification

INTERVENTIONAL

Study Start Date

2018-08-25

Study Completion Date

2019-06-25

Brief Summary

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The need to restore water losses resulting from physical activity has become established and diffused into international consensus for healthy individuals or high-performance athletes. However, the influence of fluid replacement when administered during and after exercise on cardiorespiratory parameters, cardiac autonomic modulation, and subjective perceptions of effort and pain of individuals with autonomic alterations known as the coronary arteries remain poorly understood. In this sense, this study intends to investigate the influence of hydration on cardiac autonomic modulation, cardiorespiratory parameters, subjective perception of exertion and pain of coronary arteries submitted to aerobic exercise in the model of a cardiovascular rehabilitation session. A total of 31 individuals will be recruited in this study and will perform four standardized cardiovascular rehabilitation sessions. Only in the second and the fourth session will the volunteers be instructed to ingest a quantity of water predetermined by the evaluator, based on the loss of body mass measured in the first and the third sessions. The outcomes (autonomic modulation, cardiorespiratory variables and perceptions) will be evaluated before, during and after exercise. The results of this study will enable professionals working with this population to implement awareness strategies on the importance of fluid intake in cardiovascular rehabilitation programs.

Detailed Description

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Conditions

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Coronary Artery Disease

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

OTHER

Blinding Strategy

NONE

Study Groups

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Control group in supine position

Intervention:

\- Only treadmill aerobic exercise with 60 min recovery in supine position

Group Type ACTIVE_COMPARATOR

Treadmill aerobic exercise in supine position

Intervention Type OTHER

The volunteers will be submitted to a cardiovascular rehabilitation session with 40 minutes of treadmill aerobic exercise followed by 60 minutes of recovery at the supine position.

Hydration group in supine position

Interventions:

* Treadmill aerobic exercise with 60 min recovery in supine position
* Water intake

Group Type EXPERIMENTAL

Treadmill aerobic exercise and water intake in supine position

Intervention Type OTHER

The volunteers will be submitted to a cardiovascular rehabilitation session with 40 minutes of treadmill aerobic exercise and water intake followed by 60 minutes of recovery at the supine position.

Control group in orthostatic position

Intervention:

\- Only treadmill aerobic exercise with 10 min recovery in orthostatic position

Group Type ACTIVE_COMPARATOR

Treadmill aerobic exercise in orthostatic position

Intervention Type OTHER

The volunteers will be submitted to a cardiovascular rehabilitation session with 40 minutes of treadmill aerobic exercise followed by 10 minutes of recovery at the orthostatic position.

Hydration group in orthostatic position

Interventions:

* Treadmill aerobic exercise with 10 min recovery in orthostatic position
* Water intake

Group Type EXPERIMENTAL

Treadmill aerobic exercise and water intake in orthostatic position

Intervention Type OTHER

The volunteers will be submitted to a cardiovascular rehabilitation session with 40 minutes of treadmill aerobic exercise and water intake followed by 10 minutes of recovery at the orthostatic position.

Interventions

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Treadmill aerobic exercise in supine position

The volunteers will be submitted to a cardiovascular rehabilitation session with 40 minutes of treadmill aerobic exercise followed by 60 minutes of recovery at the supine position.

Intervention Type OTHER

Treadmill aerobic exercise and water intake in supine position

The volunteers will be submitted to a cardiovascular rehabilitation session with 40 minutes of treadmill aerobic exercise and water intake followed by 60 minutes of recovery at the supine position.

Intervention Type OTHER

Treadmill aerobic exercise in orthostatic position

The volunteers will be submitted to a cardiovascular rehabilitation session with 40 minutes of treadmill aerobic exercise followed by 10 minutes of recovery at the orthostatic position.

Intervention Type OTHER

Treadmill aerobic exercise and water intake in orthostatic position

The volunteers will be submitted to a cardiovascular rehabilitation session with 40 minutes of treadmill aerobic exercise and water intake followed by 10 minutes of recovery at the orthostatic position.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Men with coronary heart disease ischemia, over 45 years
* At least three months of cardiovascular rehabilitation

Exclusion Criteria

* smokers, alcoholics
* Uncontrolled metabolic disease (eg, uncontrolled diabetes and thyroid diseases)
* Abnormal hemodynamic responses during exercise such as disproportionate increase / fall of heart rate and / or blood pressure to low / high levels of load
* myocardial ischemia and / or severe ventricular arrhythmias during the exercise test
Minimum Eligible Age

45 Years

Eligible Sex

MALE

Accepts Healthy Volunteers

No

Sponsors

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Universidade Estadual Paulista Júlio de Mesquita Filho

OTHER

Sponsor Role lead

Responsible Party

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Luiz Carlos Marques Vanderlei

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Luiz Carlos Marques Vanderlei, PhD

Role: STUDY_DIRECTOR

Universidade Estadual Paulista - UNESP - Campus de Presidente Prudente

Locations

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Luiz Carlos Marques Vanderlei

Presidente Prudente, São Paulo, Brazil

Site Status

Countries

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Brazil

Other Identifiers

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54864716800005402

Identifier Type: -

Identifier Source: org_study_id

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