- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07590258
A Single Pole Dancing Session and Its Effects on Blood Pressure
A Single Session Of Pole Dance Reduces Blood Pressure In Women
Study Overview
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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-
Santa Catarina
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Florianópolis, Santa Catarina, Brazil, 88037060
- Allana Andrade Souza
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- being female;
- be aged ≥ 18 years;
- have an intermediate level of experience in PD modality, that is, be able to perform combinations of aerial movements of medium difficulty, such as performing aerial figures in the inverted position - head down;
- not having performed vigorous physical activity in the 24 hours preceding the intervention.
Exclusion Criteria:
- being pregnant;
- have injuries that limit the proposed PD session.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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No Intervention: control session
In the control session, participants remained in a sitting position, without performing any type of physical effort, for a period of 60 minutes.
They could talk, read a book, use their cell phone and drink water, but in the minutes before the measurement, they had to remain silent, still in a sitting position, without carrying out such activities.
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|
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Experimental: experimental session
In the experimental session, participants underwent a PD class lasting 60 minutes. Initially, a warm-up (~15 min) was carried out involving joint mobility movements and muscle stretching, followed by an initial part (~10) marked by muscle strengthening and resistance exercises, execution of turns and low plane transitions. The second part of the class (~15 min) was dedicated to learning and executing movements and aerial transitions using the static pole, while, in the third part of the class (~15 min), sequences of movements on the spinning pole were worked on, finishing with a passive stretch to return to calm (~5 min). At the end of the class, subjective rate of perceived exertion (RPE) was collected using the modified Borg scale [17] (0-10), with the aim of evaluating the intensity perception of the session. |
In the experimental session, participants underwent a PD class lasting 60 minutes. Initially, a warm-up (~15 min) was carried out involving joint mobility movements and muscle stretching, followed by an initial part (~10) marked by muscle strengthening and resistance exercises, execution of turns and low plane transitions. The second part of the class (~15 min) was dedicated to learning and executing movements and aerial transitions using the static pole, while, in the third part of the class (~15 min), sequences of movements on the spinning pole were worked on, finishing with a passive stretch to return to calm (~5 min). At the end of the class, subjective rate of perceived exertion (RPE) was collected using the modified Borg scale [17] (0-10), with the aim of evaluating the intensity perception of the session.
Other Names:
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Measurement of blood pressure
Time Frame: A single session
|
To perform the measurements, participants must follow the pre-collection guidelines that will be provided when scheduling visits. These guidelines include: not consuming coffee, cigarettes, alcohol, or heavy meals on the day of collection; not engaging in strenuous physical activity in the 24 hours preceding collection; and having an empty bladder. Systolic and diastolic blood pressure will be measured using a digital device (Model HEM - 7113 from Omron Healthcare, Kyoto, Japan) at five different times: "BEFORE THE INTERVENTION", "IMMEDIATELY AFTER THE INTERVENTION", "15 MINUTES AFTER THE INTERVENTION", "30 MINUTES AFTER THE INTERVENTION", and "45 MINUTES AFTER THE INTERVENTION", all with the participant seated. At rest, three systolic and diastolic blood pressure measurements will be taken, with a one-minute interval between them. The systolic and diastolic blood pressure measurement protocol will be used equally in both sessions (experimental and control). |
A single session
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Collaborators and Investigators
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
Additional Relevant MeSH Terms
- Nervous System Diseases
- Vascular Diseases
- Cardiovascular Diseases
- Primary Dysautonomias
- Autonomic Nervous System Diseases
- Orthostatic Intolerance
- Hypotension
- Behavior
- Post-Exercise Hypotension
- Motor Activity
- Motor Activity
- Movement
- Musculoskeletal Physiological Phenomena
- Musculoskeletal and Neural Physiological Phenomena
- Exercise
Other Study ID Numbers
- POLEDANCESTUDY
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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