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Turkish Validity and Reliability of the Bolus Residue Scale in Acute Stroke

NCT07435441 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 40

Last updated 2026-02-27

No results posted yet for this study

Summary

This study aims to evaluate the validity and reliability of the Turkish version of the Bolus Residue Scale (BRS) in patients with acute stroke. The study has a methodological, observational, and cross-sectional design. Videofluoroscopic swallowing study (VFSS) recordings will be scored independently by trained raters using the BRS. Psychometric properties including construct validity, criterion validity, inter-rater and intra-rater reliability will be analyzed.

Conditions

  • Post-stroke
  • Dysphagia
  • Videofluoroscopy
  • Scale Reliability Validity

Interventions

OTHER

No intervention (observational study)

This study does not involve any therapeutic, behavioral, or procedural intervention. All assessments were performed as part of routine clinical care, and no changes were made to standard treatment or clinical management.

Sponsors & Collaborators

  • Hacettepe University

    collaborator OTHER

  • Istinye University

    collaborator OTHER

  • Atlas University

    collaborator OTHER

  • Istanbul Arel University

    lead OTHER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-08-01
Primary Completion
2026-01-15
Completion
2026-02-20

Countries

  • Turkey (Türkiye)

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07435441 on ClinicalTrials.gov