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Not Yet RecruitingNCT06576947

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

Effects of Virtual Reality in the Treatment of Pelvic Floor Dysfunction in Women With Multiple Sclerosis: A Randomized Clinical Trial

Status
Not Yet Recruiting
Phase
N/A
Study type
Interventional
Enrollment
45 (estimated)
Sponsor
Universidad de Almeria · Academic / Other
Sex
Female
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

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.

Detailed description

* Design: Randomized Clinical Trial. Objective: to determine the effects of virtual reality versus posterior tibial nerve stimulation and muscle activation exercises on the improvement of pelvic floor dysfunctions in women with multiple sclerosis. * Methods and Measures: forty five women will be randomly assigned to one of three groups. * Intervention: For 8-week, the group 1 will undergo treatment with virtual reality (2/week), the group 2 will receive posterior tibial nerve stimulation (2/week) and the group 3 will receive muscle activation exercises of the pelvic floor. * Main Outcome Measures: assessment of pelvic floor muscles function (strength and muscle tone), urodynamic studies, and validated questionnaires data will be collected at baseline, and 1 week after the last therapy application. Mixed-model analyses of variance will be used to examine the effects of the treatment on each outcome measure.

Conditions

Interventions

TypeNameDescription
OTHERVirtual realityParticipants receive virtual reality treatment, 8 weeks of treatment/ 2 times a week
OTHERNeuromodulation of the tibialis posterior nerveParticipants receive neuromodulation of the tibialis posterior nerve8 weeks of treatment/ 2 times a week/ 30 minutes
OTHERPelvic floor muscle trainingParticipants receive pelvic floor muscle training 5 times a day for 9 weeks

Timeline

Start date
2024-09-01
Primary completion
2025-07-01
Completion
2025-12-01
First posted
2024-08-29
Last updated
2024-08-29

Source: ClinicalTrials.gov record NCT06576947. Inclusion in this directory is not an endorsement.