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Contact the study team using the details below to take part. If there are no contact details below please ask your doctor in the first instance.
Provisional assignment of new diseases of uncertain etiology
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Little is known about the pattern and severity of musculoskeletal pain after COVID-19 and their association with pre-existing musculoskeletal conditions. This cross-sectional observational study aims to investigate the pattern and severity of musculoskeletal pain after COVID-19, characterise this pain and examine its relationship to pre-existing conditions, and impact on quality-of-life. Patients currently under the care of, or referred to, Leeds Community Healthcare Trust with symptoms of Long COVID will be invited to take part. Those who wish to participate will be asked to provide informed consent and to complete a questionnaire (including eligibility, personal details, ethnicity, employment, activity and work related health, Adapted LCH Post COVID-19 Rehabilitation questionnaire, Adapted Nordic Musculoskeletal Questionnaire, Pain detect, Musculoskeletal health questionnaire, and EQ-5D-5L) to report on their musculoskeletal problems, pain, and quality of life. Approximately 200-300 participants will be recruited over 12 months. Detailed descriptive analysis of the cohort to assess the distribution of various clinical and demographic variables will be evaluated.
Start dates may differ between countries and research sites. The research team are responsible for keeping the information up-to-date.
The recruitment start and end dates are as follows:
Observational type: Cross-sectional;
You can take part if:
You may not be able to take part if:
• Any physical or mental condition or disorder, which, in the opinion of the clinician at LCHT, may affect participation in the study.
Below are the locations for where you can take part in the trial. Please note that not all sites may be open.
The study is sponsored by University of Leeds and funded by NIHR / UKRI .
Your feedback is important to us. It will help us improve the quality of the study information on this site. Please answer both questions.
Read full details
for Trial ID: CPMS 51354
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