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NCT05984095Completed

Multiple Sclerosis Pelvic Floor Telerehabilitation

Pelvic Floor Rehabilitation in Females With Multiple Sclerosis: Comparison of Two Telerehabilitation Protocols

Source: ClinicalTrials.gov · Last updated 28 Nov 2023

Brief summary (registry, in English)

The goal of this clinical trial is to compare the effects of two different pelvic floor telerehabilitation protocols on selected measures of quality of life and health in females with relapsing-remitting Multiple Sclerosis (rrMS). The main questions it aims to answer are: * Is telerehabilitation sufficient to improve quality of life and health in females with rrMS, in particular dedicated to pelvic floor training? * Are self-administered training protocols or remotely-supervised training protocols equally effective? Participants will be randomized to two intervention groups: a self-administered training protocol (SELF) and a remotely-supervised (REMOTE) training protocol. Both protocols will consist in 10 sessions of pelvic floor training lasting 45 min each, once every 5 days. At the start and at the end of the protocol, all participants will complete 6 questionnaires regarding pain, quality of life and health.

Status (registry)
Completed
Study type
Interventional
Enrollment
28 (actual)
First submitted
1 Aug 2023
Start date
15 Sept 2023
Primary completion date
15 Nov 2023
Lead sponsor
University of Trieste
NCT number
NCT05984095

What you commit to

  • Study type: Interventional
  • Participants enrolled: 28
  • From 15 Sept 2023 to the primary completion date, 15 Nov 2023
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • previous history of bladder or urogynaecological surgery
  • previous history of major abdominal surgery

Other

  • females in menopause
  • females with a delivery \< 6 months from the start of the study
  • BMI \> 30

Who the study is looking for

  • diagnosis of relapsing remitting Multiple Sclerosis confirmed by a neurologist and based on the McDonald criteria from not less than 1 y
  • EDSS \<4.5
  • self reported symptoms of urinary incontinency

Age in the registry: 18 years to 50 years · Sex: Female · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
CdL in Fisioterapia
Coordinator of this site? Confirm its status
TriesteItalyUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.