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Virtual Reality in the Treatment of Pelvic Floor Dysfunction in Women With Multiple Sclerosis

NCT06576947 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 45

Last updated 2024-08-29

No results posted yet for this study

Summary

The purpose of the current randomized clinical trial was to compare the effectiveness of virtual reality versus posterior tibial nerve stimulation on the improvement of pelvic floor dysfunctions in women with multiple sclerosis.

Conditions

Interventions

OTHER

Virtual reality

Participants receive virtual reality treatment, 8 weeks of treatment/ 2 times a week

OTHER

Neuromodulation of the tibialis posterior nerve

Participants receive neuromodulation of the tibialis posterior nerve8 weeks of treatment/ 2 times a week/ 30 minutes

OTHER

Pelvic floor muscle training

Participants receive pelvic floor muscle training 5 times a day for 9 weeks

Sponsors & Collaborators

  • Universidad de Almeria

    lead OTHER

Principal Investigators

  • Guadalupe Molina Torres · Universidad de Almeria

  • Jacobo Ángel Rubio-Arias · Universidad de Almeria

  • Marta María Córdoba Peláez · Universidad de Almeria

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-09-01
Primary Completion
2025-07-01
Completion
2025-12-01

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06576947 on ClinicalTrials.gov