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Acute Effect Of Pilates On Blood Pressure In Women

Acute Effect Of Pilates Exercises On Blood Pressure In Women: A Randomized Crossover Trial

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07819058
Enrollment
15
Registered
2026-09-14
Start date
2024-08-01
Completion date
2024-12-31
Last updated
2026-09-14

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

Conditions

Elevated Blood Pressure

Keywords

Blood Pressure; Hypertension; Pilates; Exercise; Ambulatory Blood Pressure Monitoring; Acute Exercise

Brief summary

The objective of this randomized crossover clinical trial was to evaluate the acute effect of a Pilates exercise session on blood pressure in women aged 50 years or older. The main questions investigated were: * Did a single Pilates exercise session alter blood pressure in the 24 hours following the intervention? * Did the effects of Pilates on blood pressure differ from those observed after a treadmill walking session? All participants initially underwent a control condition, which involved a health history assessment and the fitting of a blood pressure monitor for 24-hour ambulatory blood pressure monitoring (ABPM). Following this condition, participants were randomly assigned to one of two intervention sequences: Pilates followed by walking, or walking followed by Pilates. The two interventions were performed with a six-day interval between sessions. In the Pilates condition, participants performed a session lasting approximately 50 minutes, consisting of 10 exercises. In the walking condition, they performed approximately 50 minutes of treadmill walking at an intensity corresponding to 60-70% of their maximum heart rate. After each experimental condition, blood pressure was monitored for 24 hours using ABPM.

Detailed description

This randomized crossover clinical trial investigated the acute effect of a single Pilates exercise session on ambulatory blood pressure in women aged 50 years or older with elevated blood pressure. The study was conducted through three experimental sessions. In the first session, all participants underwent the control/baseline condition, which included clinical and sociodemographic assessment, familiarization with the assessment procedures, and baseline blood pressure measurements. An ambulatory blood pressure monitoring device was then fitted and maintained for 24 hours without exercise, establishing the control condition. Following the control/baseline session, participants were randomly assigned to one of two intervention sequences: Pilates followed by walking or walking followed by Pilates. A six-day interval was maintained between the experimental sessions. Thus, all participants completed both exercise interventions, but the order of the interventions was randomized. The walking session was performed on a treadmill for 50 minutes at an individually prescribed intensity of 60-70% of heart rate reserve. Heart rate was continuously monitored throughout the session, and treadmill speed was adjusted as necessary to maintain the target intensity. The Pilates session was performed on a mat using body weight and a Magic Circle accessory. The session lasted 50 minutes and consisted of 10 exercises involving the trunk, upper limbs, and lower limbs. Each exercise was performed for one set of 10 repetitions, with a one-minute interval between exercises. Participants were previously instructed and familiarized with the correct execution of the exercises. After each exercise session, ambulatory blood pressure was monitored for 24 hours. Monitoring began at 2:00 PM and included measurements during both waking and sleeping periods. Participants maintained their usual medication regimen throughout the study and recorded relevant daily information, including medication use, meals, sleep and wake times, and stressful events, in an activity diary. Heart rate, perceived exertion, satisfaction, and affective responses were also assessed during the exercise sessions to characterize the physiological and subjective responses to the two exercise modalities. The study was conducted in accordance with ethical principles for research involving human participants and received approval from the Research Ethics Committee under opinion number 4.170.827. All participants provided informed consent before participation.

Interventions

BEHAVIORALPilates Exercise

A single 50-minute Pilates exercise session was performed on a mat using body weight and a Metalife Magic Circle. The session consisted of 10 exercises, with one set of 10 repetitions for each exercise and a 1-minute interval between exercises. The exercises targeted mobility, flexibility, strengthening, and trunk and lower- and upper-limb movements. Participants were previously familiarized with the exercises and instructed on their proper execution.

BEHAVIORALWalking Exercise

A single 50-minute walking session was performed on a treadmill. Exercise intensity was individually prescribed at 60-70% of heart rate reserve, with continuous heart rate monitoring throughout the session. Treadmill speed was progressively adjusted as needed to maintain the target heart rate range.

Sponsors

Universidade Estadual do Norte do Parana
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
50 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Women aged 50 years or older. * Elevated blood pressure or hypertension, regardless of antihypertensive medication use. * No injury or health condition that prevented participation in the exercise protocols. * Agreement not to engage in other physical exercise during the study period. * Willingness to participate in all study procedures and provide informed consent.

Exclusion criteria

* Failure to participate in or complete any of the study protocols or exercise sessions. * Ambulatory blood pressure monitoring errors that compromised the analysis of the study outcomes.

Design outcomes

Primary

MeasureTime frameDescription
24-hour ambulatory blood pressure24 hours after each experimental conditionTwenty-four-hour ambulatory blood pressure was assessed after each experimental condition using ambulatory blood pressure monitoring. Systolic and diastolic blood pressure were recorded throughout the 24-hour monitoring period, including waking and sleeping periods, to evaluate the acute effects of Pilates and walking on blood pressure.

Secondary

MeasureTime frameDescription
Systolic Blood Pressure24 hours after each conditionSystolic blood pressure was assessed using 24-hour ambulatory blood pressure monitoring after each condition. Mean values were evaluated for the total 24-hour period and separately for waking and sleeping periods to compare the acute responses to Pilates, treadmill walking, and the control condition.
Diastolic Blood Pressure24 hours after each conditionDiastolic blood pressure was assessed using 24-hour ambulatory blood pressure monitoring after each condition. Mean values were evaluated for the total 24-hour period and separately for waking and sleeping periods to compare the acute responses to Pilates, treadmill walking, and the control condition.
Mean Arterial Pressure24 hours after each conditionMean arterial pressure was assessed using 24-hour ambulatory blood pressure monitoring after each condition. Mean values were evaluated for the total 24-hour period and separately for waking and sleeping periods to compare the acute responses to Pilates, treadmill walking, and the control condition.
Pulse Pressure24 hours after each conditionPulse pressure was assessed using 24-hour ambulatory blood pressure monitoring after each condition. Mean values were evaluated for the total 24-hour period and separately for waking and sleeping periods to compare the acute responses to Pilates, treadmill walking, and the control condition.
Affective ValenceDuring each 50-minute exercise sessionAffective response was assessed during each exercise session using an 11-point bipolar Affective Valence Scale ranging from -5 (very bad) to +5 (very good), with 0 representing a neutral state. The scale was administered at 10 time points during each exercise session.

Countries

Brazil

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 15, 2026