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Evaluating the Feasibility of a Web-App for Pelvic Floor Health in Pregnant Women in the Ferrol Health Area: the WaPRUIN Study

Evaluating the Feasibility of a Web-App for Pelvic Floor Health in Pregnant Women in the Ferrol Health Area: the WaPRUIN Study

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06797323
Acronym
WaPRUIN
Enrollment
212
Registered
2025-01-28
Start date
2025-03-10
Completion date
2025-11-30
Last updated
2025-01-28

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

Conditions

Pelvic Floor Disorder, Pregnancy

Brief summary

This study aims to evaluate the feasibility of using a web-based application to improve pelvic floor health in pregnant women within the Ferrol Health Area, Spain. The intervention involves providing educational resources through a user-friendly digital platform, designed to empower women with knowledge about pelvic floor function and techniques for strengthening it during pregnancy. The study hypothesizes that a web-based educational tool can effectively increase awareness, engagement, and adherence to pelvic floor exercises among pregnant women, thereby contributing to improved maternal health outcomes. Participants will include pregnant women from the Ferrol Health Area, who will voluntarily use the application during their pregnancy. The study will assess outcomes related to usability, accessibility, and participant satisfaction with the application, as well as any improvements in pelvic floor-related health indicators. By addressing an important gap in maternal health education, this project has the potential to provide an innovative and scalable solution to enhance prenatal care.

Interventions

BEHAVIORALWeb-Based Application for Pelvic Floor Health

A user-friendly web application designed to provide educational resources, exercises, and interactive tools aimed at improving pelvic floor health in pregnant women.

Sponsors

Universidad de Oviedo
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Healthy volunteers
No

Inclusion criteria

* Pregnant women attending their first prenatal consultation at the Hospital Arquitecto Marcide. * Pregnant women who voluntarily consent to participate in the study by signing the informed consent form.

Exclusion criteria

* Pregnant women who do not have proficiency in the Spanish language. * Limitations in using the web-app (e.g., physical, cognitive, or technological barriers). * Lack of internet access.

Design outcomes

Primary

MeasureTime frameDescription
Feasibility of the Web-App UsageFrom enrollment to the end of web application use at 8 weeksTo evaluate the feasibility and usability of the PelviEduca web-app, which is designed to improve knowledge about pelvic floor health and related conditions during pregnancy in pregnant women within the Ferrol Health Area.

Secondary

MeasureTime frameDescription
Frequency of Web-App UseFrom enrollment to the end of web application use at 8 weeksTo analyze the frequency of use of the web-app by the participants during the study.
Relationship Between Usability and Participant CharacteristicsFrom enrollment to the end of web application use at 8 weeksTo describe the relationship between the feasibility and usability of the web-app and the personal characteristics of the participants.
Knowledge Improvement on Pelvic Floor HealthFrom enrollment to the end of web application use at 8 weeksTo evaluate whether the use of the web-app contributes to an increase in knowledge regarding pelvic floor health during pregnancy among participants.
Effectiveness in Encouraging Pelvic Floor ExercisesFrom enrollment to the end of web application use at 8 weeksTo determine the effectiveness of the web-app in promoting the practice of pelvic floor exercises among participants.
Prevalence of Urinary Incontinence at InclusionAt baseline (time of enrollment)To describe the percentage of pregnant women presenting urinary incontinence at the time of enrolment in the study

Countries

Spain

Contacts

Primary ContactRaquel Iglesias-Méndez
medicinaraquel@gmail.com+34 626754452

Outcome results

None listed

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