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Clinical Trials/NCT06384716
NCT06384716UnknownNot Applicable

Evaluation of the Influence of a Core Muscle Control-Based Rehabilitation Program on Pelvic Floor Function in Patients With Multiple Sclerosis

Universidad Europea de Madrid1 site in 1 country32 target enrollmentStarted: February 19, 2024Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Sponsor
Enrollment
32
Locations
1
Primary Endpoint
Difference in the percentage of initial and final maximum activity of the pelvic floor muscles.

Study Overview

Brief Summary

Given the structural relationship of the CORE as a whole, in this study we propose an intervention based on the global motor control of all the structures that make up the CORE to assess its effectiveness on urinary incontinence, sexual dysfunction and balance, as well as its relationship with respiratory function. According to our hypothesis, a global intervention could also be taken into account during conventional treatment in the future, helping to prevent genitourinary dysfunctions derived from alterations in motor control.

Detailed Description

Main objective:

To establish the effect of core motor control training on pelvic floor functionality in patients with multiple sclerosis.

Specific objective: To assess the effect of core motor control training on urinary incontinence.

  • To assess the effect of core motor control training on urinary incontinence in patients with multiple sclerosis.
  • To assess the effect of core motor control training on quality of life in patients with multiple sclerosis.
  • To assess the effect of core motor control training on sexual dysfunction in patients with multiple sclerosis.
  • To assess the effect of core motor control training on balance in patients with multiple sclerosis.
  • To test the relationship between respiratory functionality and pelvic floor dysfunctions in patients with multiple sclerosis.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Investigator)

Eligibility Criteria

Ages
18 Years to 70 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • - Age between 18 and 70 years.
  • Confirmed diagnosis of Multiple Sclerosis based on McDonald criteria, with an evolution time of more than two years (remitting or progressive) (24).
  • Multiple Sclerosis Disability Status Scale (EDSS) score between 2 (minimal disability in one of the functional systems), and 7.5 (inability to take more than a few steps. Limited to wheelchair and transfer support. Ability to move the chair, but not all day if the chair is conventional and lacks a motor) (25, 26).
  • Stable medical treatment for at least six months prior to surgery (26).
  • Absence of cognitive impairment, with ability to understand instructions and score 24 or higher on the Minimental Test (27).
  • Urinary incontinence as a consequence of neurological involvement.

Exclusion Criteria

  • - Diagnosis of another neurological disease or musculoskeletal disorder other than MS.
  • Diagnosis of any cardiovascular, respiratory, genitourinary, metabolic or other conditions that may interfere with this study.
  • Having presented urinary incontinence prior to the diagnosis of MS.
  • Have suffered an exacerbation or hospitalisation in the last 3 months before starting the assessment protocol, or during the therapeutic intervention process.
  • Have received a course of intravenous or oral steroids 6 months prior to the start of the assessment protocol and within the intervention period of the study duration.

Outcomes

Primary Outcomes

Difference in the percentage of initial and final maximum activity of the pelvic floor muscles.

Time Frame: 8 weeks

EMG

- Differences between the initial and final thickness of the oblique abdominis and transverse oblique muscles by ultrasound.

Time Frame: 8 weeks

US

- Differences in the assessment of health-related quality of life before and after the intervention measured with the I-QOL questionnaire.

Time Frame: 8 weeks

IQOL

- Differences in the assessment of female UI before and after intervention using the I-CIQ questionnaire

Time Frame: 8 weeks

I-CIQ

Secondary Outcomes

  • - Difference between initial and final FVC/- Differences between the initial and final peak expired volume (FEV1)(8 weeks)
  • differences between peak expiratory pressure (PEM) and minimum initial and end inspiratory pressure (MIP).(8 weeks)
  • - Difference in the percentage of initial and final maximum activity of the paravertebral musculature activity.(8 weeks)
  • - Differences between initial and final amplitude of initial and final diaphragmatic excursion by ultrasound.(8 weeks)
  • balance(8 weeks)

Investigators

Sponsor
Universidad Europea de Madrid
Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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