NCT07435441Completed
Turkish Validity and Reliability of the Bolus Residue Scale in Acute Stroke
Turkish Validity and Reliability of the Bolus Residue Scale (BRS) in Patients With Acute Stroke
Source: ClinicalTrials.gov · Last updated 27 Feb 2026
Brief summary (registry, in English)
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.
- Status (registry)
- Completed
- Study type
- Observational
- Enrollment
- 40 (actual)
- First submitted
- 20 Feb 2026
- Start date
- 1 Aug 2025
- Primary completion date
- 15 Jan 2026
- Lead sponsor
- Istanbul Arel University
- Diseases
- Stroke
- NCT number
- NCT07435441
What you commit to
- Study type: Observational
- Participants enrolled: 40
- From 1 Aug 2025 to the primary completion date, 15 Jan 2026
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other illness
- History of head and neck cancer or head and neck surgery
- Pre-existing neurological diseases affecting swallowing (e.g., Parkinson's disease, amyotrophic lateral sclerosis)
- Severe cognitive impairment preventing cooperation with assessment procedures
Other
- Structural abnormalities of the upper aerodigestive tract
- Incomplete or poor-quality VFSS recordings unsuitable for analysis
Who the study is looking for
- Diagnosis of acute stroke confirmed by neurological and radiological evaluation
- Age 18 years and older
- Undergoing videofluoroscopic swallowing study (VFSS) as part of routine clinical assessment
- Ability to participate in swallowing assessment procedures
- Provision of written informed consent by the patient or a legal representative
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Istanbul Arel University Coordinator of this site? Confirm its status | Istanbul | Turkey (Türkiye) | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.