Actively Recruiting

Age: 18Years +
All Genders
NCT06853366

Validation of the Short Form of the "Lower Urinary Tract Symptoms Treatment Constraints Assessment" Questionnaire

Led by Centre Hospitalier de Saint-Denis · Updated on 2025-02-28

242

Participants Needed

2

Research Sites

92 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

For many years, the evaluation of treatments has been a central issue in patient care. The various domains assessed have gradually evolved over time, ranging from satisfaction, improvement and quality of life, to the more recent introduction of the Patient Reported Outcome Measure (PROM). These questionnaires or measurement scales (PROMs) focus assessment on the patient and his or her direct experience. Statistical validation of numerous assessment tools has made it possible to quantify objectively many areas of assessment that were initially linked to the patient's feelings, and therefore to their subjectivity. Thus, improvement, quality of life, patient expectations and goal attainment have been the preferred areas for the development of these PROMs. However, certain areas have been sidelined in the creation of these tools. For example, the constraint of care or the side effects or negative effects of care have not been studied through specific means of evaluation. In response to this shortcoming, we have developed a questionnaire specifically designed for neuro-urological treatments in a neurological patient population. The LUTS-TCA (Lower Urinary Tract Symptoms Treatment Constraints Assessment) was developed in French and statistically validated in 2019. The aim of the study is to create a short form of the LUTS TCA in French, in a population of neurological patients. This short form, which would be easier to use and interpret, would simplify its use in everyday practice. Indeed, a large majority of neuro-urology patients suffer from neurodegenerative or progressive pathologies, marked by significant and disabling physical and psychological fatigue symptoms. Long-form questionnaires, or the addition of multiple assessment questionnaires during a single visit to the department, make overall assessment more complex. In addition, this short-form questionnaire is presented in a slightly different form to the long-form version, showing several domains of constraint (physical, social, psychological and care system). This classification should simplify the interpretation and understanding of care constraint, by and for patients. For the patient, the validation study will take place in 2 phases: * A first phase at the time of the consultation (Day 0): response to the questionnaires making up the study, i.e. the short form of the LUTS TCA (appendix 2), then the validated form of the LUTS TCA (22 questions) and finally the PGI (two questions). * A second phase, at a distance from the consultation (Day 14 post-consultation): response to the short form of the LUTS TCA (questionnaire handed out at the consultation, accompanied by a stamped envelope for return).

CONDITIONS

Official Title

Validation of the Short Form of the "Lower Urinary Tract Symptoms Treatment Constraints Assessment" Questionnaire

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adult patients (age 9 18 years)
  • Patients with central or peripheral neurological pathology, followed and managed for vesico-sphincter disorders
  • Patients receiving urinary treatment for more than 3 months
  • No therapeutic modification between D0 and D14 of the questionnaire
  • French-speaking patients (able to read, write and understand French)
Not Eligible

You will not qualify if you...

  • Minor patients (age 9 17 years)
  • Patients who have stopped urinary treatment
  • Patients with major cognitive impairment
  • Patients who speak little or no French
  • Patients who refused to participate in research, or who objected to the use of their data for research purposes

AI-Screening

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Trial Site Locations

Total: 2 locations

1

La pitié salpêtrière

Paris, paris, France, 75013

Actively Recruiting

2

Casanova Hospital

Saint-Denis, Seine saint denis, France, 93205

Not Yet Recruiting

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How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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