ClinicalTrials.Veeva

Menu

Benefits Evaluation of Selfia® Adapted Underwear for MS Patients Performing Self-catheterization (KML)

L

Lille Catholic University

Status

Withdrawn

Conditions

Multiple Sclerosis

Treatments

Device: Evaluation of underwear Selfia®

Study type

Interventional

Funder types

Other

Identifiers

NCT02889419
RC-P0045

Details and patient eligibility

About

KML is a multicenter, prospective, uncontrolled and before/after study. The study aims to estimate if the use of Selfia ® adapted underwear reduces the necessary duration for the realization of self-catheterisation (SC) for patients affected by multiple sclerosis with severe to moderate disability.

Secondly, the study aims to :

  • Estimate the effect of underwear on quality of life, tiredness linked to the act, comfort in the realization of SC, complications with SC, third party intervention ;
  • Collect patients' opinion on the use of the underwear SELFIA ® at the end of the 2nd week of evaluation ;
  • Measure if the patient reused underwear and if he bought it at 6 months and at 1 year

Full description

Bladder-sphincter disorders affect 80 % of the patients suffering from multiple sclerosis (MS) after 10 years of evolution and urinary self-catheterization (SC) are part of the therapeutic arsenal.

SC involves different steps: the preparation of the material, the undressing, the transfer on toilets, the technical gesture and the dressing. Recommendations of good practice of SC of the French Society of Physical Medicine and Rehabilitation evoke the necessity to adapt the wardrobe but without precision on the definition of this adaptation.

Adapted underwear exists for patients with a disability and is accessible for the general public. However, no clinical trial has ever evaluated their real practical interest for disabled patients realizing SC.

These undergarments, according to our experience, are very ingenious and would bring a real comfort in everyday life from patients with a disability.

In case of SC, this underwear would facilitate and shorten the time dedicated to this technique, especially as SC are realized on average 6 times a day for patients already affected in their movements because of their initial handicap.

The adapted underwear could bring an ease and a speed of dressing / undressing, allow an easier and faster access to the urinary meatus and a limitation of manipulations and mobilizations of the patient allowing an energy saving.

Moreover, disabled patients request concrete advice from health professionals on everyday life problems such as dressing / undressing. Therefore it seemed interesting to estimate the benefits of using adapted underwear for the realization of SC for patients affected by MS with severe to moderate disability (EDSS 6 - 7.5) affecting everyday life activities.

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients with multiple sclerosis (MS) according to McDonald criteria
  • At least 18 years old
  • Self-catheterization for at least 3 months
  • Expended Disability Status Scale (EDSS) between 6.0 and 7.5
  • Informed consent
  • Coverage of the social insurance

Exclusion criteria

  • MS relapse in the previous month
  • Patient hospitalized in short stay or aftercare departments, no matter the reason
  • Morbid obesity (BMI superior to 35)
  • Understanding disorders preventing an informed consent
  • EDSS inferior to 6.0 or superior to 7.5
  • Patient with home bladder catheter
  • No capacity to provide a self-catheterisation
  • Age under 18 years
  • Pregnant or breast-feeding woman
  • Patient under legal protection

Trial design

Primary purpose

Supportive Care

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

0 participants in 1 patient group

Evaluation of underwear Selfia®
Experimental group
Description:
Every patient is his own control.
Treatment:
Device: Evaluation of underwear Selfia®

Trial contacts and locations

6

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems