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Validation of the French Version of the Sydney Swallow Questionnaire in Patients With Neuromuscular Diseases

Not Applicable
Completed
Conditions
Dysphagia
Neuromuscular Diseases
Interventions
Other: Sydney Swallow Questionnaire
Registration Number
NCT02845362
Lead Sponsor
Cliniques universitaires Saint-Luc- Université Catholique de Louvain
Brief Summary

Measurements of dysphagia severity are important when making management decisions and in the objective evaluation of swallowing impairments. The Sydney Swallow Questionnaire (SSQ) is a validated self-report inventory using a visual analogue scale. This questionnaire permits a quantitative, sensitive, specific, repeatable and easily responsive evaluation of dysphagia in different pathology. Opposed to largely used videofluoroscopy swallowing study and endoscopy examinations, the SSQ is noninvasive, less expensive, avoids radiation exposure and enables a readily available assessment. Validated French version is not yet available. In the first phase of the study the investigators will validated this translation in dysphagic patients and control. Secondly, the investigators will validate the SSQ in Neuromuscular patients.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
250
Inclusion Criteria

Phase 1:

Group 1:

  • Healthy participants
  • Able to speak, read and write in French
  • Aged at least 18 years old

Group 2:

  • Patients, with symptoms indicative of a deglutition disorder, referred for a videofluoroscopic study to the Otolaryngology, Head and Neck Surgery Department, Voice and Swallowing Clinic
  • Able to speak, read and write in French
  • Aged at least 18 years old

Phase 2:

  • Clinical diagnosis of neuromuscular diseases
  • Able to understand French
Exclusion Criteria

Phase 1:

Group 1:

  • History of neurological or neuromuscular disease
  • History of any diagnosticated swallowing disorder

Group 2:

  • Patients who could not be cataloged as dysphagic or non-dysphagic after the videofluoroscopic study evaluation
  • Patients unable to answer the questionnaire

Phase 2:

  • Patients who could not be cataloged as dysphagic or non-dysphagic
  • Patients unable to answer the questionnaire

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Dysphagia assessmentSydney Swallow Questionnaire-
Primary Outcome Measures
NameTimeMethod
Sydney Swallow Questionnaire10 minutes

The participants were asked to fill out these questionnaires during the outpatient visit.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (2)

Cliniques universitaires Saint-Luc

🇧🇪

Brussels, Belgium

Cliniques universitaires Saint Luc

🇧🇪

Brussels, Belgium

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