- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06529354
24-Week Water Aerobics Program for Adults and Older Adults at Different Intensity Levels
The Role of Exercise Intensity in Water Aerobics: Improving Health Markers in Adults and Older Adults Over 24 Weeks
This goal of this clinical trial is to verify the best way to do water aerobics with adults and older adults. It wants to answer these questions:
- Is high-intensity water aerobics better than water aerobics performed at moderate intensity?
- Does a 24-week water aerobics program improve muscle strength, body weight, fat mass, triglycerides, cholesterol, blood pressure, and quality of life for adults and older adults?
Participants must:
- Do water aerobics at high or moderate intensity, twice a week for 45 minutes per class, for 24 weeks.
- Be assessed before starting the water aerobics program and after it ends to see if there are gains in muscle strength, body weight, fat mass, triglycerides, cholesterol, blood pressure, and quality of life.
It was believed that all variables would get better after doing water aerobics, no matter the intensity. It was also expected that doing higher-intensity water aerobics would lead to larger gains in all measurements compared to moderate-intensity.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
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Abrantes, Portugal, 2205-700
- Tramagal Municipal Swimming Pool
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- At least 18 years of age
Exclusion Criteria:
- taking part in another physical exercise program
- being recently hospitalized
- having severe motor or cognitive problems
- having any medical restrictions on physical exercise
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Moderate-intensity Group
Participants engaged in 45-minute water aerobics sessions twice a week for 24 weeks at moderate intensities.
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In water aerobics sessions, the exercises are performed at a moderate intensity, between 60% and 70% of the participant's maximum heart rate predicted by their age.
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Experimental: High-intensity Group
Participants engaged in 45-minute water aerobics sessions twice a week for 24 weeks at high intensities.
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In water aerobics sessions, the exercises are performed at a high intensity, between 80% and 90% of the participant's maximum heart rate predicted by their age.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change from Baseline in explosive strength of lower limbs at 24 weeks
Time Frame: Baseline and week 25
|
The countermovement jump was used to assess the explosive strength of the lower limbs.
Participants were instructed to perform three countermovement jumps, aiming to jump as high as possible, with one minute of rest between each jump.
A higher jump height indicates a better score in this evaluation.
The mean value of the three jumps was considered for the test.
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Baseline and week 25
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Change from Baseline in explosive strength of upper limbs at 24 weeks
Time Frame: Baseline and week 25
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The explosive strength of the upper limbs was measured by having participants throw a 3-kilogram medicine ball, with the best scores achieved by throwing the ball as far as possible.
Three throws were performed, and the mean value was used in this test.
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Baseline and week 25
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Change from Baseline in endurance strength of lower limbs at 24 weeks
Time Frame: Baseline and week 25
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The chair stand test was used to evaluate the endurance strength of the lower limbs.
Participants sat in the center of a chair with a straight back and feet shoulder-width apart and in full contact with the floor.
They then rose to maximum extension and returned to the initial sitting position, aiming to complete as many repetitions as possible within a 30-second.
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Baseline and week 25
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Change from Baseline in endurance strength of upper limbs at 24 weeks
Time Frame: Baseline and week 25
|
The arm curl test assessed the upper limbs' endurance strength.
Participants were seated in a chair with a straight back and their feet flat on the floor, holding a 2 kg dumbbell in their dominant hand.
They were instructed to perform as many correct flexions as possible within a 30-second time limit.
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Baseline and week 25
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Change from Baseline in body mass at 24 weeks
Time Frame: Baseline and week 25
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A bioimpedance balance was used for this test, with participants being barefoot and dressed in minimal clothing.
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Baseline and week 25
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Change from Baseline in fat mass percentage at 24 weeks
Time Frame: Baseline and week 25
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Baseline and week 25
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Change from Baseline in fat-free mass at 24 weeks
Time Frame: Baseline and week 25
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Baseline and week 25
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Change from Baseline in body mass index at 24 weeks
Time Frame: Baseline and week 25
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The body mass index (BMI) was calculated by dividing the body mass value by the height squared (kg/m^2).
For this, each participant's height was measured using a precision stadiometer with a scale of 0.001 m.
For the correct extraction of this test, participants were barefoot.
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Baseline and week 25
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Change from Baseline in triglycerides at 24 weeks
Time Frame: Baseline and week 25
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Blood samples were collected before exercise (after a 15-minute rest period) and at least 2 hours after the last meal.
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Baseline and week 25
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Change from Baseline in total cholesterol at 24 weeks
Time Frame: Baseline and week 25
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Baseline and week 25
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Change from Baseline in diastolic blood pressure at 24 weeks
Time Frame: Baseline and week 25
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The automatic blood pressure monitor was used to measure the participants' blood pressure after seated and rested for 20 minutes.
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Baseline and week 25
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Change from Baseline in systolic blood pressure at 24 weeks
Time Frame: Baseline and week 25
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Baseline and week 25
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Change from Baseline in resting heart rate at 24 weeks
Time Frame: Baseline and week 25
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Resting heart rate was assessed using an automatic blood pressure monitor, after the participant was seated and resting for at least 20 minutes.
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Baseline and week 25
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change from Baseline in quality of life at 24 weeks
Time Frame: Baseline and week 25
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The WHOQOL-BREF (Portuguese version) questionnaire, consisting of 26 items, was used to evaluate the participants' quality of life.
Of the 26 items, 2 pertain to general quality of life and general health, while the remaining 24 items assess the perception of quality of life in 4 domains: physical, psychological, social relationships, and environment.
Higher scores indicate a higher quality of life in each domain.
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Baseline and week 25
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Luís Faíl, University of Beira Interior
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- CE-UBI-Pj-2019-051
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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