Dysphagia and Dysphonia Outcomes in SARS CoV-2 (COVID-19) Infection (DYADS Study)
NCT04584658 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 50
Last updated 2025-06-29
Summary
This study examines the presence, severity and natural history of dysphagia and dysphonia in the post-extubation and severely unwell COVID-19 patient.
Conditions
- Dysphagia
- Dysphonia
- Subglottic Stenosis
- Voice Disorders
- Swallowing Disorder
- Covid19
- SARS (Severe Acute Respiratory Syndrome)
- SARS Pneumonia
- Quality of Life
- SARS-CoV-2 Infection
Interventions
- DIAGNOSTIC_TEST
-
Fibreoptic Endoscopic Evaluation of Swallowing (FEES)
This is the use of endoscopy during feeding trials. The patient is fed different consistencies of food and drink while an endoscope is in place (usually passed through the nasal passage and down into the throat). The endoscope provides a bird's eye view to the transit of food through the upper aero-digestive tract. This provides information from the point of food bolus formation in the mouth to the movement of the base of the tongue; the movement of pharyngeal muscles; the deflection of the epiglottis to protect the airway including the closure of the vocal cords and the passage of food into the oesophagus. Any abnormality in these steps are noted during FEES. Liquids, thickened fluids, semi-solids and solids are some of the food textures that are tested.
- DIAGNOSTIC_TEST
-
Videofluoroscopy
A radio opaque dye is used to label the test food and drink items offered to the patient. Following this, x-ray technology is used to create a video of the outline of the patient and the structures responsible for chewing and swallowing as they injest the test materials. The study is carried out in real time in the radiology department in conjunction with a radiographer and an SLT.
- OTHER
-
Dysphagia Handicap Index (DHI)
This is a 25-item questionnaire assessing three domains: physical (9 items), functional (9 items), and emotional aspects (7 items) of the Quality of Life (QOL) in patients suffering with dysphagia. For each statement the patient checks if it applies to him/her all the time, some of the time or never. The suggested scores are 0, 2 and 4, respectively. Using this scoring system amounts to a DHI score range of 0 - 100. The higher the score, the worse the dysphagia related QOL. The patient is also asked to provide a rating of their own impression of the severity of the dysphagia experienced on a scale from 1 (normal) to 7 (severe problem).
- OTHER
-
Voice Symptom Scale (VoiSS)
This is a 30-item validated quality of life tool that is also a self-reporting tool. It appraises the impact of the patient's abnormal voice from an emotional perspective, related physical symptoms and stratifies the impairment itself in context of day to day activities. VoiSS is currently the most psychometrically robust voice outcome measure. Each item is scored 0 - 4 on the frequency responses: never, occasionally, some of the time, most of the time, always. The total score of 120 measures general voice pathology which is made up of Impairment = maximum score of 60; Emotional = maximum score of 32; Physical = maximum score of 28.
Sponsors & Collaborators
-
Cambridge University Hospitals NHS Foundation Trust
lead OTHER
Eligibility
- Min Age
- 18 Years
- Max Age
- 85 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2020-09-15
- Primary Completion
- 2022-11-30
- Completion
- 2023-01-30
Countries
- United Kingdom
Study Locations
More Related Trials
-
Dysphagia Management During COVID-19 Pandemic
NCT04509752 ·Status: COMPLETED
-
DYsphagiA in interMedIate Care UnitS
NCT04180449 ·Status: ACTIVE_NOT_RECRUITING
-
Pulsed Dye Laser in Treating Patients With Post Radiation Dysphonia
NCT02198131 ·Status: COMPLETED ·Phase: NA
-
Dysphagia and VFMI in Cardiac Patients
NCT03768739 ·Status: COMPLETED
-
High Dose Steroids for Dysphagia
NCT03256149 ·Status: WITHDRAWN ·Phase: NA
-
Voice and Swallow Outcomes After Office-based Injection Laryngoplasty in Patients With Glottal Insufficiency
NCT06161064 ·Status: NOT_YET_RECRUITING ·Phase: NA
-
A Study on Building a Voice Cohort for the Development of a Non-face-to-face Machine Learning Diagnostic and Monitoring Platform Using Voice Analysis and Various Sensors in Patients With Dysphagia.
NCT05439447 ·Status: COMPLETED
-
Dysphagia and Vocal Cord Injury Following Cardiac Surgery
NCT04464317 ·Status: WITHDRAWN
-
Establishment of Voice Analysis Cohort for Development of Monitoring Technology for Dysphagia
NCT05149976 ·Status: RECRUITING
-
Gender Disparities in Voice Outcomes After Tracheoesophageal Puncture in Total Laryngectomy Patients (UC Davis)
NCT05489965 ·Status: RECRUITING
-
Using the Subglottic Pressure to Predict the Dysphagia After Partial Laryngectomy
NCT06024980 ·Status: RECRUITING ·Phase: NA
-
Dysfunction Following Thyroid Surgery
NCT04087447 ·Status: UNKNOWN
-
Relationship Between Swallowing Dynamics and Suprahyoid Muscle Activity in Sarcopenic Dysphagia
NCT07198568 ·Status: RECRUITING
-
Screening for Sarcopenic Dysphagia and the Implementation of Measures to Prevent Its Complications in Geriatric Patients [DYSPHAGING-PILOT]
NCT05734586 ·Status: RECRUITING ·Phase: NA
-
Effect of Intravenous Corticosteroid Injections on Dysphagia After Cervical Spine Surgery
NCT02266797 ·Status: TERMINATED ·Phase: PHASE3
-
Effect of Local Intraoperative Steroid on Dysphagia After ACDF
NCT03311425 ·Status: COMPLETED ·Phase: PHASE3
-
Swallowing Evaluation in VF Immobility
NCT05473169 ·Status: UNKNOWN
-
Respiratory-Swallow Coordination in Cardiothoracic Surgical Patients
NCT05173207 ·Status: COMPLETED
-
Treatment Alternatives in iSGS (NoAAC PR-02 Study)
NCT02481817 ·Status: COMPLETED
-
Goitres Influence on Voice Function - The Impact of Surgery
NCT02468921 ·Status: UNKNOWN
-
Functional Collagen Scaffold for Laryngeal Soft Tissue Regeneration
NCT04164485 ·Status: UNKNOWN ·Phase: PHASE1/PHASE2
-
Comparison of the Swallowing Functions in Sarcopenia and Dynapenia
NCT04960007 ·Status: UNKNOWN
-
Functional Voice and Speech Outcomes Following Surgical Voice Restorations: A Comparison of Pharyngeal Construction Approaches
NCT00600223 ·Status: COMPLETED
-
Voice Quality Analysis of Patients With Laryngotracheal Stenosis
NCT06161077 ·Status: NOT_YET_RECRUITING
-
Evaluating the Feasibility of Acapella® Choice as a Dysphonia Treatment
NCT04764604 ·Status: COMPLETED ·Phase: NA