Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
100 participants
OBSERVATIONAL
2022-04-30
2024-12-31
Brief Summary
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Detailed Description
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The purpose of this study is to investigate the clinical characteristics, etiopathological mechanisms and the natural course of pain, and to understand its physical and psychosocial consequences. We will also analyse the correlation of pain to clusters of long COVID symptoms. We anticipate the results of this study will help the healthcare providers to deliver adequate management for patients with long COVID.
This is a longitudinal study to observe 100 patients with long COVID pain throughout an 18-month period. Pain assessment will be undertaken using validated methods, that include blood tests to detect inflammatory biomarkers, clinical examination, standardised pain instruments/scales, Quantitative Sensory Testing to measure changes in sensitivity, and electroencephalography to measure brain network activity. Physical activity measurements include Timed Up and Go Test to assess balance and mobility, Rated Perceived Exertion Scale to measure exercise intensity, and Hand-Grip Dynamometer test to measure handgrip strength. In addition, we will use psychological assessment tools to assess the severity of depression and anxiety, and self-efficacy and pain-related thoughts.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Prospective cohort
Patients with long COVID and new-onset musculoskeletal pain
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
2. New onset musculoskeletal pain that develops during or following an infection consistent with COVID-19, continues for 4 weeks or more and is not explained by an alternative diagnosis.
3. Age 18 years or older.
4. Ability of participant to understand and the willingness to sign a written informed consent document.
5. Stated willingness to comply with all study procedures and availability for the duration of the study.
6. Ability of participant to read and understand English.
Exclusion Criteria
2. Unable to provide informed consent.
3. Specific exclusion for Electroencephalogram (EEG): Patients with history of epileptic seizures.
18 Years
ALL
No
Sponsors
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Leeds Comunity Healthcare NHS Trust
OTHER
University of Leeds
OTHER
Responsible Party
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Dr Manoj Sivan
Associate Professor and Consultant in Rehabilitation Medicine
Principal Investigators
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Manoj Sivan, MD
Role: PRINCIPAL_INVESTIGATOR
University of Leeds
Locations
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Leeds Teaching Hospitals NHS Trust
Leeds, England, United Kingdom
Leeds Community Healthcare NHS Trust
Leeds, England, United Kingdom
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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296125
Identifier Type: -
Identifier Source: org_study_id
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