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New scale could help turkish doctors spot swallowing problems after stroke

NCT ID NCT07435441

Knowledge-focused Sponsor: Istanbul Arel University Source: ClinicalTrials.gov ↗

What the study statuses mean

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study checked if a Turkish version of the Bolus Residue Scale (BRS) is a reliable way to measure swallowing problems in people who recently had a stroke. Researchers looked at video recordings of 40 patients swallowing and had experts rate the results. The goal was to make sure the scale works well in Turkish, so doctors can better assess and treat swallowing issues after a stroke.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Participants

40 people

The number who actually took part.

Started

Aug 2025

Finished

Feb 2026

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Who is studied

The study population consisted of adult patients with acute stroke who were referred for videofluoroscopic swallowing study (VFSS) as part of routine clinical care. All participants underwent swallowing assessment using standardized residue and swallowing scales. No intervention was applied, and all evaluations were conducted within standard clinical practice.

Ages

18 years and older

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * 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 Exclusion Criteria: * 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) * Structural abnormalities of the upper aerodigestive tract * Severe cognitive impairment preventing cooperation with assessment procedures * Incomplete or poor-quality VFSS recordings unsuitable for analysis

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Conditions

The condition(s) this trial relates to.

Deglutition Disorders stroke disorder

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Dysphagia Post stroke Scale reliability validity Videofluoroscopy

Contacts and locations

Locations

  • Istanbul Arel University

    Istanbul, Zeytinburnu, 34015, Turkey (Türkiye)

More trials for these conditions

Other studies related to the condition(s) this trial covers.