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Effects of Aquatic Exercise on Post-exercise Hypotension

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ClinicalTrials.gov Identifier: NCT03403478
Recruitment Status : Completed
First Posted : January 18, 2018
Last Update Posted : July 5, 2019
Sponsor:
Collaborator:
University Center of Joao Pessoa - UNIPE
Information provided by (Responsible Party):
Bruno Teixeira Barbosa, Federal University of Paraíba

Brief Summary:
This is a randomized controlled trial. The present study involves an acute and chronic intervention, which is a water-based exercise (one session: to acute intervention; 12-weeks of aquatic exercise program: to chronic intervention). The sample will be composed by elderly enrolled in university extension program titled "Hidroginastica na Terceira Idade" (Hydrogymnastics in aging). It will be evaluated the effects of water-based exercise on hemodynamics, self-reported sleep quality, depressive symptoms, quality of life, body composition, level of physical activity and functional capacity. The investigators hypothesized that an acute water-based exercise under different intensities promotes hemodynamics changes in elderly. In addition, the investigators hypothesized that 12-weeks of aquatic exercise may lead improvements in self-reported sleep quality, depressive symptoms, quality of life, body composition, level of physical activity and functional capacity in elderly.

Condition or disease Intervention/treatment Phase
Hypertension Aging Obesity Other: LICE Other: MICE Other: HIIE Other: Aquatic exercise training Not Applicable

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 20 participants
Allocation: Randomized
Intervention Model: Crossover Assignment
Masking: Single (Participant)
Masking Description: To acute session, the participant will not be informed about what aquatic exercise session (light-, moderate-, high-intensity or control) intensity will be performed.
Primary Purpose: Treatment
Official Title: Effects of Aquatic Exercise on Post-exercise Hypotension
Actual Study Start Date : March 1, 2018
Actual Primary Completion Date : October 31, 2018
Actual Study Completion Date : October 31, 2018

Resource links provided by the National Library of Medicine


Arm Intervention/treatment
No Intervention: Control group
The volunteers will be instructed to remain in an orthostatic position immersed in water up to the imaginary line of the xiphoid process for 45 minutes without performing jerky body movements.
Experimental: LICE
The light-intensity continuou exercise (LICE) session comprises a 45-minute of guide walking into the pool at 55-60% of maximum heart rate (HRmax). The HR will be checked every 2 minutes during the whole session.
Other: LICE
No specific exercise will be performed. The participant will walk into the pool accompanied with a researcher for 45 minutes.

Experimental: MICE
The moderate-intensity continuous exercise (MICE) will bem performed divided into 3 phases: warm-up (10 minutes), main part (30 minutes) and cool down (5 minutes). The warm-up and cool down will be performed at 55-60% HRmax. The main part will last 30 minutes and will be performed by 3 sets of 5 exercises lasting 2 minutes each one at 70-75% HRmax. For all phases, HR will be measured every 2 minutes during the whole session.
Other: MICE

The following exercises will be carried out: a) jumping jacks (shoulder abduction and adduction); b) horizontal adduction and abduction of the shoulder; c) stationary running with knee elevation; d) pull and push horizontally with upper limbs; e) pull and push vertically with upper limbs.

Note: For exercises 'a' and 'b', the legs alternated in movements in the sagittal plane to provide greater stability to the participant's movement. For exercises 'd' and 'e', the legs simulates a stationary running.


Experimental: HIIE
The high-intensity intervaled exercise (HIIE) will bem performed divided into 3 phases: warm-up (10 minutes), main part (15 minutes) and cool down (5 minutes). The warm-up and cool down will be performed at 55-60% HRmax. The main part will last 15 minutes and will be performed by 2 sets of 5 exercises lasting 30 seconds to each exercise combined with 1 minute of active recovery. The exercise moment will be performed at 80-85% HRmax and the 1-minute active recovery at 55-60% HRmax. For both warm-up and cool down, HR will be measured every 2 minutes. For main part, HR will be measured at the end of each 30-seconds from exercise.
Other: HIIE

The following exercises will be carried out: a) jumping jacks (shoulder abduction and adduction); b) horizontal adduction and abduction of the shoulder; c) stationary running with knee elevation; d) pull and push horizontally with upper limbs; e) pull and push vertically with upper limbs.

Note: For exercises 'a' and 'b', the legs alternated in movements in the sagittal plane to provide greater stability to the participant's movement. For exercises 'd' and 'e', the legs simulates a stationary running.


Experimental: Aquatic exercise training
The participants will be submitted to a 12-weeks of aquatic exercise program, twice a week, for 1 hour each day.
Other: Aquatic exercise training

The sessions of the aquatic exercise training will be divided into 3 phases: warm-up (10 minutes), main part (40 minutes) and cool down.

In order to increase intensity to aquatic exercise, the training program will carried out as follows:

From week 1 to 4 the instructors will use a 128 bpm musics in both warm-up and cool down. In main part, will be used a 130 bmp musics.

From week 5 to 8 the instructors will use a 130 bpm musics in both warm-up and cool down. In main part, will be used a 132 bmp musics.

From week 9 to 12 the instructors will use a 132 bpm musics in both warm-up and cool down. In main part, will be used a 135 bmp musics.





Primary Outcome Measures :
  1. Blood pressure [ Time Frame: Entire day (an average of 24 hours). ]
    The blood pressure will be measured by a Ambulatory Blood Pressure Monitoring (ABPM).

  2. Blood pressure [ Time Frame: Up to 1 hour post-exercise session ]
    The blood pressure will be measured by an automatic blood pressure device (OMRON HEM-720).


Secondary Outcome Measures :
  1. Self-reported sleep quality [ Time Frame: Approximately 15 minutes ]
    Pittsburgh Sleep Quality Index

  2. Depressive symptoms (Mental disorders) [ Time Frame: Approximately 5 minutes ]
    Geriatric depressive symptoms (GDS-15) is a validated questionnaire which will be used in order to evaluate depressive symptoms in elderly.

  3. Self-reported quality of life [ Time Frame: Approximately 15 minutes ]
    Quality of life will be assessed by the WHOQOL-OLD questionnaire and it consists of 24 items on the likert scale attributed to 6 facets: 1) Sensory functioning, 2) Autonomy, 3) Past, present and future activities, 4) Social participation, 5) Death and dying, and 6) Intimacy. Each facet is composed of 4 items, so for each facet the score can range from 4 to 20. For this evaluation, the higher the score, the higher the quality of life.

  4. Level of physical activity (BAECKE modified to elderly) [ Time Frame: Approximately 5 minutes ]
    The Habitual Physical Activity Questionnaire originated in 1982 by Baecke and colleagues (BAECKE; BUREMA, FRIJTERS, 1982) and was adapted for the elderly and validated later (VORORRIPS et al., 1991) and recently translated into Portuguese (SIMÕES, 2009). It is applied in the form of an interview, and has as reference the last 12 months being divided into 3 sections (1 - Domestic physical activities, 2 - Sporting activities and 3 - Activities in free time). From the scores attributed to each response provided by the elderly, scores equivalent to each section cited above are established. It is suggested that 3 cutoff points be created for the classification of the elderly regarding the level of physical activity (low, moderate and high) based on terciles.

  5. Functional Capacity [ Time Frame: Approximately 35 minutes ]
    AAPHERD test battery



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Ages Eligible for Study:   60 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Elderly (60 years and over)
  • Able to practice physical exercise in water
  • Able to answer all questionnaires
  • Non-smoker

Exclusion Criteria:

  • Morbid obese
  • Those who not complete all data collection procedures

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03403478


Locations
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Brazil
Bruno Teixeira Barbosa
Joao Pessoa, Paraíba, Brazil, 58051420
Sponsors and Collaborators
Federal University of Paraíba
University Center of Joao Pessoa - UNIPE
Investigators
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Principal Investigator: Bruno T Barbosa, Master University Center of Joao Pessoa - UNIPE
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Responsible Party: Bruno Teixeira Barbosa, Assistant Professor, Federal University of Paraíba
ClinicalTrials.gov Identifier: NCT03403478    
Other Study ID Numbers: 79609117.0.0000.5188
First Posted: January 18, 2018    Key Record Dates
Last Update Posted: July 5, 2019
Last Verified: July 2019
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Keywords provided by Bruno Teixeira Barbosa, Federal University of Paraíba:
Hemodynamics
Aquatic exercise
Elderly
Additional relevant MeSH terms:
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Post-Exercise Hypotension
Hypotension
Vascular Diseases
Cardiovascular Diseases
Orthostatic Intolerance
Primary Dysautonomias
Autonomic Nervous System Diseases
Nervous System Diseases