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HIIH Versus HMC: Randomized Clinical Trial

Not Applicable
Recruiting
Conditions
Healthy People
Interventions
Other: Hydrogynmastics Continuous Moderate
Other: High-intensity interval Hydrogynmastics
Registration Number
NCT03293056
Lead Sponsor
Universidade Federal do vale do São Francisco
Brief Summary

Introduction: water aerobics involves the practice of specific aquatic exercises that are based on the use of water resistance as a load and on thrust as an impact reducer, making it possible to perform physical exercise with a lower risk of injury even at a high intensity. Objective: The overall objective of this study will be to compare the effectiveness of high intensity interval versus moderate continuous water aerobics to improve health outcomes in apparently healthy individuals.

Detailed Description

Method: randomized clinical trial will be performed in the premises of the College of Physical Education of the Federal University of the São Francisco Valley. 100 adults, of both sexes, will be randomized into two groups, high intensity interval hydrogynastic (HIAI) or moderate continuous aquatic gymnastics (HCM). Individuals will be evaluated for primary endpoints of muscle strength and endurance, aerobic fitness, flexibility and body composition. The secondary outcomes evaluated will be the quality of life, functionality and perception of improvement by a Likert-type Improvement Scale, at the following moments: initial, final and follow-up of one month after the end of the training. Individuals will be assisted for three months, often weekly twice, with sessions lasting 50 min. In order to identify differences between and within the groups, an equation of generalized estimates will be used as regression model with the syntax according to the multivariate model.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
75
Inclusion Criteria
  • age between 18 and 60 years;
  • sedentary and who did not perform physiotherapy and physical activity in the last three months;
  • clinical and cognitive conditions for swimming pool activities and aerobic exercise; who have not undergone highly complex surgical procedures in the last six months;
  • to be able of walking without help equipment and without musculoskeletal or skeletal diseases;
  • without contraindications to the practice of exercises; such as: urinary and / or fecal incontinence and dermatological diseases;
  • below obesity II with BMI <40.
Exclusion Criteria
  • if they have up to three consecutive fouls during the hydrogymnastics period;
  • if they present any adverse effects, such as: allergy or any dermatitis;
  • unable to continue the study due to change of address or hospitalization.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Hydrogynmastics Continuous ModerateHydrogynmastics Continuous ModerateHydrogynmastics Continuous Moderate training (HCM), 2x/week, for 3 months.
High-intensity Interval HydrogynmasticsHigh-intensity interval HydrogynmasticsHigh-intensity Interval training Hydrogynmastics, 2x/week, for 3 months.
Primary Outcome Measures
NameTimeMethod
Aerobic Fitnessthree months after randomization

This maximal/submaximal test will be performed on cyclergometer, Balke test.

Body Compositionthree months after randomization

The body composition (density and percentage of body fat) will be estimated by prediction equations (JACKSON et al., 1980).

Endurance Muscularthree months after randomization

Muscle endurance will be assessed by the test in which the individual performs the maximum number of repetitions of given exercises for one minute. The exercises will be of arm and abdominal flexion.

Strength Muscularthree months after randomization

Strength Muscular will be measured by 1RM test in two exercises, involving the segments of the upper limbs (supine) and lower limbs (leg press).

Secondary Outcome Measures
NameTimeMethod
Quality Lifethree months after randomization

Quality of life by assessed by WHOQOL-breaf

Functionalitythree months after randomization

Functionality will be assessed by IVCF-20

Perception of Improvementthree months after randomization

Perception of Improvement will be measured by an Likert-type Improvement Scale

Trial Locations

Locations (1)

Physical Education College

🇧🇷

Petrolina, Pernambuco, Brazil

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