- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06871280
Assessment of Vertigo and Dizziness in Individuals Following COVID-19
March 10, 2025 updated by: Istanbul Physical Medicine Rehabilitation Training and Research Hospital
This cross-sectional study aimed to assess the prevalence of dizziness/vertigo in individuals following COVID-19 and to investigate potential risk factors associated with these symptoms.
A total of 296 patients aged 20-66 years who had recovered from COVID-19 were evaluated at Istanbul Physical Medicine and Rehabilitation Training and Research Hospital between June 1, 2021, and December 31, 2021.
Clinical and demographic data, including COVID-19 history, comorbidities, and symptom characteristics, were collected.
Dizziness-related disability was assessed using the Dizziness Handicap Inventory (DHI), while balance performance was evaluated with the Berg Balance Scale (BBS).
Study Overview
Status
Completed
Conditions
Study Type
Observational
Enrollment (Actual)
296
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Istanbul, Turkey
- Istanbul Physical Medicine Rehabilitation Training and Research Hospital
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
N/A
Sampling Method
Probability Sample
Study Population
This study included 296 patients aged 20-66 years who had recovered from COVID-19 and presented to the outpatient clinic
Description
Inclusion Criteria:
- Individuals aged 20-66 years.
- History of confirmed COVID-19 infection.
- Ability to speak and understand Turkish.
- Willingness to provide verbal and written informed consent.
Exclusion Criteria:
- Pre-existing vertigo or balance disorders (e.g., benign paroxysmal positional vertigo, Ménière's disease, vestibular migraine, vestibular neuritis).
- Inner ear diseases or vestibular dysfunction.
- Neurological disorders affecting balance (e.g., multiple sclerosis, Parkinson's disease, history of stroke, epilepsy).
- Psychiatric conditions that could cause dizziness (e.g., anxiety, panic attacks, depression).
- History of head or neck trauma in the past six months.
- Moderate to severe visual impairment.
- Chronic alcohol or substance use.
- Use of ototoxic medications.
- Severe cardiovascular diseases (e.g., orthostatic hypotension, advanced heart failure, severe arrhythmias).
- Pregnant or breastfeeding women.
- Acute infection other than COVID-19 in the past three months.
- Severe COVID-19 requiring hospitalization
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Dizziness Handicap Inventory
Time Frame: 0 day
|
Prevalence of dizziness/vertigo in individuals following COVID-19, assessed using the Dizziness Handicap Inventory (DHI). Range: 0-100 (Higher scores indicate greater dizziness-related disability). |
0 day
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Berg Balance Scale (BBS)
Time Frame: 0 day
|
Balance status evaluated using the Berg Balance Scale (BBS).
Range: 0-56 (Higher scores indicate better balance)
|
0 day
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
June 1, 2021
Primary Completion (Actual)
December 31, 2021
Study Completion (Actual)
December 31, 2021
Study Registration Dates
First Submitted
March 10, 2025
First Submitted That Met QC Criteria
March 10, 2025
First Posted (Actual)
March 25, 2025
Study Record Updates
Last Update Posted (Actual)
March 25, 2025
Last Update Submitted That Met QC Criteria
March 10, 2025
Last Verified
March 1, 2025
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Neurologic Manifestations
- Nervous System Diseases
- Respiratory Tract Infections
- Infections
- RNA Virus Infections
- Virus Diseases
- Respiratory Tract Diseases
- Lung Diseases
- Pneumonia, Viral
- Pneumonia
- Coronavirus Infections
- Coronaviridae Infections
- Nidovirales Infections
- Otorhinolaryngologic Diseases
- Sensation Disorders
- Ear Diseases
- Labyrinth Diseases
- Vestibular Diseases
- COVID-19
- Vertigo
- Dizziness
Other Study ID Numbers
- IstanbulPMRTRH222
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.