ClinicalTrials.gg
Enrolling by invitationNCT07639580Updated Jun 10, 2026

Urinary Incontinence and Low Energy Avaliability in Professional and Pre-professional Dancers: a Cross-sectional Study

An observational study in Urinary Incontinence and RED-S, sponsored by University of Siena. Enrolling by invitation at 1 site in Italy. Open to female participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-06-10.

Sponsored by University of Siena · Observational

Study type
Observational
Model
Cohort
Time perspective
Cross-sectional
Enrollment
60
Ages
18 Years and older
Sex
Female
01

Study summary

The purpose of this study is to describe the prevalence of Urinary Incontinence amongst professional and pre-professional dancers and its relation to Low Energy Avaliability

Read the detailed description

Urinary incontinence is a widespread issue among the female athletic population, negatively impacting both performance and lifestyle. The discipline of dance subjects the pelvic floor to repeated stress, which, as in other sports, could lead to the development of incontinence and other pelvic symptoms. Relative Energy Deficiency in Sport (RED-S) syndrome is caused by a prolonged and problematic energy deficit, or Low Energy Availability (LEA), and could be one of the contributing factors to the development of urinary incontinence (UI). The world of professional dance is characterized by a high risk of RED-S; nonetheless, few studies have investigated the prevalence of urinary incontinence and its relationship with low energy availability in this context.

This study aims at investigating the prevalence of urinary incontinence and the risk of relative Low Energy Availability (LEA) in a population of professional and pre-professional female dancers, and secondarily, to study the correlation between these two parameters and their impact on the participants' quality of life and performance.

Data Collection: Administration of validated Italian questionnaires for self-reported urinary incontinence (International Consultation on Incontinence Questionnaire - Urinary Incontinence Short Form or ICIQ-UI SF) and for the risk of Low Energy Availability (Low Energy Availability in Females Questionnaire or LEAF-Q) via Google Forms. All data will be collected anonymously.

Statistical Analisys: Based on the data distribution (normal or non-normal), the most appropriate descriptive statistics will be used, along with Student's t-test or the Mann-Whitney test, calculating the 95% confidence interval for all variables under study (pages 4-5 of the research project).

All analyses will be conducted using SPSS (version 26 or later) and, for specific verifications, JASP (version 0.96.0).

02

Conditions studied

  • Urinary Incontinence
  • RED-S

Keywords

  • Urinary Incontinece
  • Low Energy Avaliability
  • Dancers
  • RED-S
03

In context

Urinary Incontinence

983 studies on the registry are indexed under Urinary Incontinence; 180 are open to participants now.

This study's planned enrollment of 60 is below the median of 120 across 215 observational studies indexed under Urinary Incontinence.

Browse Urinary Incontinence studies →

Lead sponsor

University of Siena is the lead sponsor of 65 studies on the registry; 15 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
Female
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Healthy professional and pre-professional dancers aged 18+

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

  • Professional dancers (must have danced professionally, with a work contract in the last 6 months) OR pre-professional student (currently enrolled in a high-level dance academy or pre-professional course)

Exclusion criteria

Exclusion Criteria:

  • Current or previous pregnancy
  • Low level of Italian or English language
05

Study design

Observational model
Cohort
Time perspective
Cross-sectional
Enrollment
60 participants (estimated)
Patient registry
No

Interventions

  • OtherICIQ-UI-SF (International Consultation on Incontinence Questionnarie - Urinary Incontinence Short Form)

    Participants will be administered 2 patient-reported outcome questionnaires

    Also known as: LEAF-Q (Low Energy Avaliability in Females Questionnaire)

06

What researchers measure

Primary outcomes

  1. Urinary Incontinence

    Prevalence of Urinary Incontinence

    Time frame: 12 months

Secondary outcomes

  1. Low Energy Avaliability

    Low energy avaliability risk is defined by a score \<8 at the LEAF-Q

    Time frame: 12 months

07

Study locations

1 site
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Started Mar 2026 (actual). Primary completion is estimated for Oct 2026, 7 months after the start.

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

Registered
Jun 4, 2026
First posted
Jun 10, 2026
StartActual
Mar 1, 2026
Primary completionEst.
Oct 30, 2026
CompletionEst.
Dec 30, 2026
Last update
Jun 10, 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 Jun 10, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07639580
Lead sponsor
University of Siena
Responsible party
Elisabetta Bigi (Physiotherapist, SPT, University of Siena) — Principal investigator
First posted
Jun 10, 2026
Start date
Mar 1, 2026
Primary completion
Oct 30, 2026 (estimated)
Completion
Dec 30, 2026 (estimated)
Last update
Jun 10, 2026

Oversight

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

Interested in this study?

Eligibility is decided by the study team. Share this record with your doctor or contact the team directly.

No contact was published for this record. The registry link below has the sponsor’s details.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion