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Virtual Bladder Training for Overactive Bladder Syndrome in Women. Which Symptom Responds Better?

Virtual Bladder Training for Overactive Bladder Syndrome in Women. Which Symptom Responds Better?

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05493748
Enrollment
86
Registered
2022-08-09
Start date
2022-05-01
Completion date
2023-12-31
Last updated
2022-08-09

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

Conditions

Overactive Bladder Syndrome

Keywords

Overactive Bladder Syndrome, Bladder Training

Brief summary

According to International Urogynecological Association and International Continence Society joint report on the terminology for female pelvic floor dysfunction, overactive bladder syndrome (OAB) is defined as urinary urgency, usually accompanied by frequency and nocturia, with or without urgency urinary incontinence, in the absence of urinary tract infection or other obvious pathology. Bladder training lasting for a minimum of 4 to 6 weeks is indicated as a first-line treatment. The investigators' goal is to compare changes in satisfaction, measured in terms of quality of life, in 2 groups of women with different main accompanying symptoms in OAB (frequency vs. nocturia), before and after bladder training utilizing telemedicine (virtual bladder training), for 4 to 6 weeks.

Interventions

Bladder training for overactive bladder syndrome.

Sponsors

Hospital Italiano de Buenos Aires
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

Quasi-experimental, before-after trial.

Eligibility

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

Inclusion criteria

* women over 18 years of age * Live in Buenos Aires City * Overactive Bladder Syndrome * Access to virtual appointment

Exclusion criteria

* Previous overactive bladder syndrome treatment. * Prior stress urinary incontinence or pelvic organ prolapse surgery. * History of Neurogenic Bladder, pelvic organs prolapse or pelvic radiation. * Pregnancy.

Design outcomes

Primary

MeasureTime frameDescription
Change in King's Health Questionnaire (KHQ) scoreChange from Baseline King's Health Questionnaire at 6 weeksKHQ score: 0-100 points per domain. Higher scores mean a worse outcome.Ten points change in KHQ score, before and after bladder training.
Change in International Consultation on Incontinence Questionnaire Short Form (ICIQ-SF) scoreChange from Baseline International Consultation on Incontinence Questionnaire Short Form at 6 weeksICIQ SF score: 0-21 points. Higher scores mean a worse outcome. Three points change in ICIQ-SF score, before and after bladder training.

Countries

Argentina

Contacts

Primary ContactAgustina Vendramini, Dra.
agustina.vendramini@hiba.org.ar5491123950443

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026