ClinicalTrials.gg
CompletedNCT07590258Updated May 15, 2026

A Single Pole Dancing Session and Its Effects on Blood Pressure

An interventional study of Pole Dance in Healthy Women Volunteers, sponsored by Universidade Federal de Santa Catarina. Completed at 1 site in Brazil. Open to female participants, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-05-15.

Primary conditionMotor Activity(the registry's first term)UnverifiedIs this wrong?Motor Activity is a broad heading, used only when no more specific condition is named. No better condition is named, so the registry's term is kept.

Sponsored by Universidade Federal de Santa Catarina · Not applicable, Interventional, and Other

From the registry’s dates

  • Registered 3 years 11 months after the study started (first participant enrolled Apr 2022, registered Apr 2026).
Phase
Not applicable
Study type
Interventional
Enrollment
21
Allocation
Randomized
Sex
Female
01

Study summary

This study aimed to evaluate the acute blood pressure (BP) response after a single pole dance (PD) session in adult women. Twenty-one young women (\<31 years old) with normal BP and previous PD experience participated. Each subject completed one experimental session (60-minute PD class) and one control session (60 minutes seated), on different days, in randomized order. Systolic blood pressure (SBP), diastolic blood pressure (DBP), and heart rate (HR) were measured at baseline, immediately after, and at 15, 30, and 45 minutes post-session.

Read the detailed description

Purpose: To evaluate the acute blood pressure (BP) response after a single session of pole dance (PD) in adult women. Material and methods: Young women (\< 31 years old), with normal BP, with previous experience in PD. Each participant performed an experimental session (ES - 60' PD class) and a control session (CS - 60' seated), on different days, in a randomized manner. In both sessions, systolic blood pressure (SBP), diastolic blood pressure (DBP) and heart rate (HR) were measured at different times: pre-session, immediately after, after 15', after 30', and after 45'. Analysis of variance for repeated measures was used to compare inter- and intra-session outcomes, with p\<0.05.

02

Conditions studied

  • Healthy Women Volunteers

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Keywords

  • Pole Dancing
  • Physical exercise
  • Post-exercise hypotension
03

In context

Motor Activity Unverified

9,798 studies on the registry are indexed under Motor Activity; 1,910 are open to participants now.

This study's enrollment of 21 is below the median of 60 across 8,388 interventional studies indexed under Motor Activity.

Browse Motor Activity studies →

Lead sponsor

Universidade Federal de Santa Catarina is the lead sponsor of 24 studies on the registry; 2 are open to participants now.

Compared within Motor Activity, the registry's first condition term, which may not be this study's main condition. Counted across the registry records on this site, refreshed daily. How we classify →

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
Female
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  1. being female;
  2. be aged ≥ 18 years;
  3. 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;
  4. not having performed vigorous physical activity in the 24 hours preceding the intervention.

Exclusion criteria

Exclusion Criteria:

  1. being pregnant;
  2. have injuries that limit the proposed PD session.
05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Randomized
Intervention model
Crossover assignment
Masking
None (open label)
Enrollment
21 participants (actual)

Study arms

  • 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.

  • 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.

    Other: Pole Dance

Interventions

  • OtherPole Dance

    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.

    Also known as: Physical exercise

06

What researchers measure

Primary outcomes

  1. Measurement of blood pressure

    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).

    Time frame: A single session

07

Study locations

1 site
  • Allana Andrade Souza
    Florianópolis, Santa Catarina 88037060, Brazil
08

References and documents

Study documents

PDFs hosted by the registry, ClinicalTrials.gov.

Individual participant data

Plan to share: No

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Ran from Apr 2022 to primary completion in Jul 2023, 15 months.

Of 5,147 non-industry interventional studies with no phase under Motor Activity, half reached primary completion within 17 months of starting (the median), counting those still running; a quarter within 7 and three quarters within 36. This study's 15 months is below that.

Counting every sponsor, half of 5,207 studies reached it within 17 months; a quarter within 7 and three quarters within 36.

How these figures are worked out, and which studies are left out of them.

Registered
Apr 3, 2026
First posted
May 15, 2026
StartActual
Apr 20, 2022
Primary completionActual
Jul 20, 2023
CompletionActual
Jul 20, 2023
Last update
May 15, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on May 15, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07590258
Lead sponsor
Universidade Federal de Santa Catarina
Responsible party
Aline Mendes Gerage (Principal Investigator, Universidade Federal de Santa Catarina) — Principal investigator
First posted
May 15, 2026
Start date
Apr 20, 2022
Primary completion
Jul 20, 2023
Completion
Jul 20, 2023
Last update
May 15, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in May 2026. You cannot join it, but the record below documents what was studied.

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