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Beach Tennis And Hypertension Study 2

Effect of Recreational Beach Tennis on Ambulatory Blood Pressure and Physical Fitness in Hypertensive Individuals (BAH Study)

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03909321
Acronym
BAH
Enrollment
42
Registered
2019-04-10
Start date
2023-02-06
Completion date
2023-12-31
Last updated
2025-11-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hypertension

Keywords

Exercise, Beach Tennis, Sport training, Ambulatory blood pressure monitoring

Brief summary

No studies have investigated the chronic effects of team sports on 24 h ambulatory blood pressure and have assessed the effects of a beach tennis intervention in cardiovascular profile and physical fitness. Based on that, the investigators designed this parallel randomized controlled trial to evaluate the effect of beach tennis training on 24 h ambulatory blood pressure and different physical fitness parameters in individuals with hypertension. The difference between the intervention arms in mean change from baseline in 24 h, daytime and nighttime systolic and diastolic ambulatory blood pressure at 12-weeks is the primary outcome; secondary outcomes are the difference between mean change in office blood pressure as well as cardiorespiratory fitness, muscular strength and power. The investigators anticipate that 12 weeks of beach tennis training will reduce blood pressure when compared to a non-exercising control group. Additionally, our recreational beach tennis intervention will improve all physical fitness components in comparison to the baseline values.

Detailed description

This is a single-center, two-arms, parallel randomized controlled trial with concealed allocation, blinded measurers, with 12 weeks of follow-up analyzed using an intention-to-treat approach. Participants will be randomly allocated to the beach tennis training intervention (BTT) or to the control group (Con), which will not be submitted to intervention and will be instructed not to engage in any kind of structured physical exercise training and to keep the life activities identified at baseline. The International Physical Activity Questionnaire (IPAQ) will be applied before and after the intervention in order to assess the level of physical activity. In BTT, supervised beach tennis sessions will be performed two times per week. Each session will be composed of an initial period of 10 min of warm up and technical exercises (i.e., serve, volley, forehand and backhand). After that, 3 games of 10-15 min each (weeks 1-4: 3 × 10 min; weeks 5-8: 3 × 12 min; and weeks 9-12: 3 × 15 min) with an interval of 2 min between each game will be played in pairs (i.e., 2 versus 2). In case of less than 4 participants are able to play at the same time, the games can also be played individually (i.e., 1 versus1). In Con, participants will be advised to not change their daily usual activities and to not participate in any structured physical exercise program during this period.

Interventions

BEHAVIORALBeach tennis training group

Beach Tennis Training Group (BTG) will perform two sessions of 40-60 min of beach tennis during 12 weeks. BT sessions will be composed by a warm up of 5-10 min of BT technical exercises (i.e., serve, volley, forehand and backhand exercises) followed by 3 BT small games of 10-15 min each.

Sponsors

Federal University of Rio Grande do Sul
CollaboratorOTHER
Hospital de Clinicas de Porto Alegre
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
35 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Office blood pressure between 130-179 and 80-110 mmHg for systolic and diastolic blood pressure, respectively; * Non-engaged in structured exercise programs in the last 3 months before the beginning of this study; * Able to perform the proposed exercises.

Exclusion criteria

* Underlying cardiovascular disease in the last 24 months such as acute myocardial infarction, angina, stroke or heart failure; * Diseases that reduce life expectancy; * Smokers; * BMI \>39.9 kg/m²; * Diabetic proliferative retinopathy.

Design outcomes

Primary

MeasureTime frameDescription
Ambulatory Blood PressureChange from baseline 24-hour systolic blood pressure at 12 weeks24h ambulatory blood pressure measured through automatic oscillometric device

Secondary

MeasureTime frameDescription
Diastolic blood pressureWill be measured during intervention period throughout the first session of weeks 1, 4, 5, 8, 9 and 12.Diastolic blood pressure in mmHg measured using automatic oscillometric device
Cardiorespiratory fitness (Oxygen consumption at peak)Change from baseline VO2peak at 12 weeksOxygen consumption at peak (VO2peak) as assessed by maximal cardiopulmonary exercise testing
Muscle strength (Test of hand grip strength)Change from baseline handgrip at 12 weeksPerforms palmar grip with the greatest possible force
Systolic blood pressureWill be measured during intervention period throughout the first session of weeks 1, 4, 5, 8, 9 and 12.Systolic blood pressure in mmHg measured using automatic oscillometric device
Power muscleChange from baseline vertical countermovement jump at 12 weeksVertical countermovement jump tests
Quality of life (WHOQOL-BREF questionnaire)Change from baseline QoL score at 12 weeksThe questionnaire contains 26 questions and is divided into four domains (physical, psychological, social and environmental). Responses follow a Likert scale (1 to 5, the higher the score the better the quality of life) and the values of each domain will be expressed in percentage values.
Enjoyment (PACES questionnaire)Will be measured during intervention period throughout the first session of weeks 1, 4, 5, 8, 9 and 12.The scale is composed of 18 items in a bipolar affirmations format (i.e., amused versus not-amused) punctuated in a range from the minimum value 1 to the maximum value 7.
Muscle strength (Chair-stand test)Change from baseline Chair-stand test at 12 weeksThe total number of stands executed correctly within 30-s

Countries

Brazil

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 24, 2026