- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05060497
DYNamic Assessment of Multi Organ Level Dysfunction in Patients Recovering From Covid-19 (DYNAMOCovid-19)
Study Overview
Status
Conditions
Detailed Description
Purpose and design Covid-19 manifests as a spectrum of multi-organ damage and dysfunction. Skeletal muscle wasting and strength loss from heightened inflammatory burden and hospital immobilisation, together with vascular dysfunction and lung damage, combine to create a profound insult resulting in severe deconditioning and long-lasting functional insufficiencies. Marked physiological deficits likely prevail due to the multi-organ nature of this insult, but clear understanding of breadth and magnitude is lacking.
Whilst susceptible groups exist, patients surviving this critical illness also include those who were previously fit and well, many of younger and working age, but a unifying trait is the inability to mount a dynamic physiological response to simple every-day activities, such as walking. Greater effort to address the multi-organ nature of this lack of physiological resilience is urgently warranted, it is essential to understand the relative regional contribution of the disease to pathophysiology and frailty. Further, understanding the dynamic response across organs will be fundamental in developing optimal interventions to facilitate recovery.
This project will combine state-of-the-art, validated techniques and research expertise in human physiology, MRI/MRS and clinical medicine to provide novel insight of the impact of Covid-19 on physiological resilience at a multi-organ level (here, muscle, heart and brain related to fatigue/physical activity), using exercise as a stressor. This will provide a unique clinically valuable perspective of whole body dysfunction that will underpin global rehabilitative programmes designed to maximise patient recovery and functionality.
The urgent priority to define Covid-19 multi-organ damage and optimise the rehabilitation package underpins the rapidity of this call.
There are other multi-organ MRI projects post Covid-19 (for example coverscan and C-More) which will take cohorts of patients. DYNAMO differs as it has been developed specifically to mechanistically study the cause for the persisting symptoms such as fatigue, atrophy, impaired exercise tolerance, poor vascular and metabolic health, and cognitive impairment and delineate the targets for rehabilitation. Detailed whole-body and organ level metabolic and physiological assessments will be collected using dynamic magnetic resonance imaging (MRI) and MR spectroscopy measures, with exercise as a stressor, only under stress will some deficits become apparent. This is highly novel, and will deliver unprecedented insight into the mechanisms driving persisting symptoms. DYNAMO will complement other projects, and the objectives and detailed physiological phenotyping described in DYNAMO is not covered elsewhere in other funded imaging studies. Moreover, DYNAMO will provide an important evidence-based foundation for optimising future rehabilitation.
Investigators will be recruiting 30 patients who have recovered from Covid-19, 5-7 months from discharge from their local hospital Trust, compared to 10 age, gender, body mass index (BMI) and ethnicity matched healthy control volunteers. Patients will also undergo a set of 6 month follow up visits to see if there is any change in their physiological and metabolic function.
Recruitment Potentially eligible patients, attending the established post Covid-19 outpatient clinic at the Nottingham University Hospitals Trust as part of their follow up care after hospital admission, will be approached by an existing member of their clinical care team (the Chief investigator (CI) forms part of this team). Similarly, there is active follow-up at other nearby acute hospital trusts in the East Midlands, who are collaborating, from where patients can be recruited. Furthermore, collaborations with PHOSP-Covid on this project have been confirmed and participants who have been involved in PHOSP-Covid can be recruited as a Tier 3 study.
Volunteers will be given a Participant Information Sheet to read about this study and will be advised that with their verbal consent, their contact details can be passed onto a research team, who can contact them to discuss the study further and answer any questions they may have. If needed, the usual hospital interpreter and translator services will be available to assist with discussion of the trial, the participant information sheets, and consent forms, but the consent forms and information sheets will not be available printed in other languages. Potential participants will be given at least 48 hours to decide on whether they wish to participate in the study.
Potential participants may also be approached by way of invitation letter sent to them from their Clinician or a member of the research team, inviting them to consider taking part. A Participant Information Sheet will also be included with this letter. Patients identified through their records by the CI who is also their clinician will be contacted by one of the clinical team who will check/confirm they are in receipt of the letter and discuss the study further, answer any queries and see if they are interested in taking part. They can also contact the study team if they are interested in taking part or leave their contact details so a research nurse can then contact them to discuss the study and /or arrange an appointment to come in for a study visit.
Investigators will also approach participants admitted following Covid-19 related hospital admission to the Nottingham University Hospitals trust, though these patients will be required to wait 5-7 months following discharge to commence study participation.
Any patient who decides to take part in the study will be given an appointment for a study visit; at the start of which, a research fellow (medic), fully trained in the study procedures and informed consent will take consent, participants will have the opportunity to speak to a medically trained doctor if they wish.
In order to recruit volunteers who haven't contracted with Covid, investigators will use our study flyer with relevant contact details, and will advertise on Nottingham University Hospitals and University of Nottingham campuses, in local press, in departmental Facebook and Twitter posts and in any departmental mailing/ emailing lists to people who have agreed to be contacted with such information. A summary of the research study will also be provided on the designated website.
It will be explained to all potential participant that entry into the trial is entirely voluntary and that their treatment and care will not be affected by their decision. It will also be explained that they can withdraw at any time but attempts will be made to avoid this occurrence. In the event of their withdrawal it will be explained that their study research data collected so far cannot be erased and investigators will seek consent to use the data in the final analyses where appropriate. It will be possible to link the withdrawn participant to the log and consent form. However, any personal information, such as contact details will be removed appropriately. Participants that are withdrawn from the study will be replaced with new volunteers.
Volunteers will undergo a series of tests including:
- Height, weight, fat and fat free mass (DEXA scan)
- Blood sampling if not already taken within 1 month of study visit, as part of routine clinical care: Full blood count, renal function including glomerular filtration rate (eGFR), troponin, brain natriuretic peptide, glycosylated haemoglobin, liver function, ferritin, creatine kinase (CK), clotting and inr, Tumour necrosis factor-alpha (TNF-alpha), interlocking-6 (IL-6) and C-reactive protein (CRP)
- Step count over 1 week using Sensewear® armband during waking hours
- Hand grip strength (hand held dynamometer) 3 measurements of grip strength using a hand held dynamometer in the dominant hand.
- Questionnaires: Fatigue severity score, quality of life (Short Form (t-36)), mental health (Personal Health Questionnaire/PHQ), frailty (Rockwood Clinical Frailty Scale/CFS) Dyspnoea-12 and Nottingham activities of daily living, and measure of cognitive state (Montreal Cognitive Assessment/ MoCA), MRI safety questionnaire, DEXA screening form
- ECG
- Arterialised blood gas: using retrograde cannulation
- Spirometry to assess basic lung function if not already done as part of routine clinical care within 1 month of study visit
- Short physical performance battery (SPPB)
- Introduction to the supine exercise equipment and familiarisation (Ergospect diagnostic pedal).
- Whole body glucose disposal during oral glucose tolerance test (OGTT). Fat and carbohydrate oxidation rates in fasting state and in response to OGTT using an indirect calorimetry ventilated hood system will be assessed. Collectively assessing metabolic flexibility, and along with body composition and intramuscular lipid content will provide a powerful index of metabolic health.
- Muscle function assessment (Isokinetic dynamometer) N= 3 maximal voluntary isometric contractions of the knee extensors interspersed with 30 seconds recovery. N=20 repeated isokinetic, knee extensor contractions at a constant angular velocity of 180o/s to determine muscle torque development and fatigue (torque loss).
- Motor unit remodelling using intramuscular EMG (iEMG) to study changes in motor unit size and functionality in the quadriceps muscle group during recovery.
- Quadriceps muscle micro-biopsy for mitochondrial content (citrate synthase maximal activity) - excess muscle tissue will be archived to quantify muscle targets of interest depending on findings
- MR measures (cardiac output, cerebral blood flow and perfusion, oxygen extraction, brain architecture, whole body fat and muscle content and skeletal muscle quality). Measures of cardiac output and structure, brain architecture (grey matter volume and cortical thickness), cerebral blood flow, perfusion, brain fractional oxygen extraction and whole-body fat and muscle volumes will be determined in the resting state. Subjects will then perform a period of steady-state low intensity supine exercise using an in-magnet exercise stepper ergometer (Ergospect diagnostic pedal), during which measures of cardiovascular and cerebrovascular physiological resilience to exercise (ability to respond) will be collected (cardiac output, left ventricular dysfunction, tagging, cerebral blood flow, perfusion and oxygenation).
- Skeletal muscle quality will be assessed using 31P magnetic resonance spectroscopy (31P MRS) of calf muscle Phosphocreatine (PCr) recovery kinetics following within-scanner plantar flexion exercises, using a MRI compatible ergometer (Trispect diagnostic pedal) and muscle proton MRS will be used to quantify intra/extra myocellular lipid content.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Contact
- Name: Ayushman Gupta, MBChB, MRCPUK
- Phone Number: 01158231702
- Email: ayushman.gupta@nottingham.ac.uk
Study Locations
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Nottinghamshire
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Nottingham, Nottinghamshire, United Kingdom, NG5 1PB
- NIHR Nottingham BRC Respiratory Theme, University of Nottingham and NUH Trust
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
Covid patients -
- Adults aged 18 years and over,
- Severe, laboratory confirmed Covid-19 infection that required hospital admission,
- 5-7 months post discharge from local hospital Trusts.
Controls -
- No active or previous Covid infection, ie no previous positive Covid PCR test and absence of active symptoms
- Matched for age, gender, BMI and ethnicity.
Exclusion Criteria:
- Absolute contraindications for MR scan
- Pre-Covid diagnosed chronic respiratory, renal, cardiovascular or cerebrovascular disease or diabetes
- BMI<20kg/m2
- Pregnancy
- Those requiring oxygen therapy or non-invasive ventilation
- Those on anticoagulation will be included but will not have a muscle biopsy
- Active arthritis
- Overt muscle damage, e.g. plasma creatine kinase > 300
- Any other conditions in addition to the above that the investigators consider may affect study measurements or safety
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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Covid patients
Participants who were treated in hospital with laboratory diagnosed Covid-19 requiring high flow oxygen, non invasive ventilation or intubation and have now recovered.
They will be recruited 5-7 months post discharge from their local hospital Trust
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Healthy control volunteers
Participants who are otherwise healthy, who have not had Covid-19 infection and are age, gender, BMI and ethnicity matched to patients
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Resting state brain structural measures - white matter and grey matter volumes
Time Frame: 5-7 months post hospital discharge for patients
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Use of MRI sequences to assess grey matter and white matter volume in patients with severe Covid-19 at 5-7 months and 11-13 months of discharge from hospital as well as non-Covid, age, gender, BMI and ethnicity matched volunteers.
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5-7 months post hospital discharge for patients
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Resting state brain structural measures - white matter microstructure
Time Frame: 5-7 months post hospital discharge for patients
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Use of MRI sequences to assess white matter tract distribution in patients with severe Covid-19 at 5-7 months and 11-13 months of discharge from hospital as well as non-Covid, age, gender, BMI and ethnicity matched volunteers.
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5-7 months post hospital discharge for patients
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Resting state cardiac structural integrity - cardiac output
Time Frame: 5-7 months post hospital discharge for patients
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Use of MRI sequences to assess cardiac output at rest in patients with severe Covid-19 at 5-7 months and 11-13 months of discharge from hospital as well as non-Covid, age, gender, BMI and ethnicity matched volunteers.
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5-7 months post hospital discharge for patients
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Resting state cardiac structural integrity - cardiac fibrosis
Time Frame: 5-7 months post hospital discharge for patients
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Use of MRI sequences to look for the degree of fibrosis at rest in patients with severe Covid-19 at 5-7 months and 11-13 months of discharge from hospital as well as non-Covid, age, gender, BMI and ethnicity matched volunteers.
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5-7 months post hospital discharge for patients
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Resting state whole-body fat and muscle volumes
Time Frame: 5-7 months post hospital discharge for patients
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Use of MRI sequence (mDixon) to assess whole-body fat and muscle content in patients with severe Covid-19 at 5-7 months and 11-13 months of discharge from hospital as well as non-Covid, age, gender, BMI and ethnicity matched volunteers.
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5-7 months post hospital discharge for patients
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Resting state myocellular fat content
Time Frame: 5-7 months post hospital discharge for patients
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Use of MR spectroscopy sequence to assess intramyocellular and extramyocellular lipid content in patients with severe Covid-19 at 5-7 months and 11-13 months of discharge from hospital as well as non-Covid, age, gender, BMI and ethnicity matched volunteers.
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5-7 months post hospital discharge for patients
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Dynamic changes in cerebral haemodynamics during low level supine in-bore exercise - cerebral blood flow
Time Frame: 5-7 months post hospital discharge for patients
|
MRI sequences will be carried out at rest, during steady-state low level in-bore supine exercise and recovery to assess changes in cerebral blood flow in patients with severe Covid-19 at 5-7 months and 11-13 months of discharge from hospital as well as non-Covid, age, gender, BMI and ethnicity matched volunteers.
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5-7 months post hospital discharge for patients
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Dynamic changes in cerebral haemodynamics during low level supine in-bore exercise - cerebral perfusion
Time Frame: 5-7 months post hospital discharge for patients
|
MRI sequences will be carried out at rest, during steady-state low level in-bore supine exercise and recovery to assess changes in cerebral perfusion in patients with severe Covid-19 at 5-7 months and 11-13 months of discharge from hospital as well as non-Covid, age, gender, BMI and ethnicity matched volunteers.
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5-7 months post hospital discharge for patients
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Dynamic changes in cerebral haemodynamics during low level supine in-bore exercise - cerebral oxygen extraction
Time Frame: 5-7 months post hospital discharge for patients
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MRI sequences will be carried out at rest, during steady-state low level in-bore supine exercise and recovery to assess changes in cerebral oxygen extraction in patients with severe Covid-19 at 5-7 months and 11-13 months of discharge from hospital as well as non-Covid, age, gender, BMI and ethnicity matched volunteers.
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5-7 months post hospital discharge for patients
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Dynamic changes in cerebral haemodynamics during low level supine in-bore exercise - cardiac output
Time Frame: 5-7 months post hospital discharge for patients
|
MRI sequences will be carried out at rest, during steady-state low level in-bore supine exercise and recovery to assess changes in cardiac output in patients with severe Covid-19 at 5-7 months and 11-13 months of discharge from hospital as well as non-Covid, age, gender, BMI and ethnicity matched volunteers.
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5-7 months post hospital discharge for patients
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Recovery kinetics of skeletal muscle phosphocreatine
Time Frame: 5-7 months post hospital discharge for patients
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Recovery kinetics of phosphocreatine (Pcr) in the gastrocnemius will be measured following its depletion using MR spectroscopy to assess skeletal muscle quality in patients with severe Covid-19 at 5-7 months and 11-13 months of discharge from hospital as well as non-Covid, age, gender, BMI and ethnicity matched volunteers.
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5-7 months post hospital discharge for patients
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Whole body glucose disposal - glucose and insulin concentrations
Time Frame: 5-7 months post hospital discharge for patients
|
Oral glucose tolerance test will be used to measure glucose and insulin concentration for whole body glucose disposal in patients with severe Covid-19 at 5-7 months and 11-13 months of discharge from hospital as well as non-Covid, age, gender, BMI and ethnicity matched volunteers.
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5-7 months post hospital discharge for patients
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Whole body glucose disposal - resting energy expenditure
Time Frame: 5-7 months post hospital discharge for patients
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Indirect calorimetry will be used to measure resting energy expenditure for whole body glucose disposal in patients with severe Covid-19 at 5-7 months and 11-13 months of discharge from hospital as well as non-Covid, age, gender, BMI and ethnicity matched volunteers.
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5-7 months post hospital discharge for patients
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Motor unit size
Time Frame: 5-7 months post hospital discharge for patients
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Intramuscular electromyography will be used to measure motor unit size in the vastus lateralis in patients with severe Covid-19 at 5-7 months and 11-13 months of discharge from hospital as well as non-Covid, age, gender, BMI and ethnicity matched volunteers.
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5-7 months post hospital discharge for patients
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Muscle mRNA
Time Frame: 5-7 months post hospital discharge for patients
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Muscle mRNA expression will be determined in skeletal muscle samples obtained from a micro biopsy of the vastus laterals in patients with severe Covid-19 at 5-7 months and 11-13 months of discharge from hospital as well as non-Covid, age, gender, BMI and ethnicity matched volunteers.
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5-7 months post hospital discharge for patients
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Clinical and demographic data
Time Frame: 5-7 months post hospital discharge for patients
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age, ethnicity, covid related hospital stay (for patients), covid related interventions (for patients), comorbidities, medications list
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5-7 months post hospital discharge for patients
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muscle strength and function
Time Frame: 5-7 months post hospital discharge for patients
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quadriceps maximum voluntary contraction using cybex dynamometer
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5-7 months post hospital discharge for patients
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hand grip strength
Time Frame: 5-7 months post hospital discharge for patients
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hand grip strength using a hand grip dynamometer will be measured
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5-7 months post hospital discharge for patients
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Short Physical performance battery test (SPPB)
Time Frame: 5-7 months post hospital discharge for patients
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SPPB will be used to assess gait speed, balance and ability to sit up from a chair.
Scores within the domains will add up to 4 with 0 being the minimum score
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5-7 months post hospital discharge for patients
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Physical activity
Time Frame: 5-7 months post hospital discharge for patients
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Measuring step count using Sensewear activity arm band
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5-7 months post hospital discharge for patients
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questionnaires for quality of life and symptoms
Time Frame: 5-7 months post hospital discharge for patients
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Fatigue severity score - min score 7 max score 63
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5-7 months post hospital discharge for patients
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questionnaires for quality of life and symptoms
Time Frame: 5-7 months post hospital discharge for patients
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Quality of life as judged by SF-36 - min score 0 max score 100
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5-7 months post hospital discharge for patients
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questionnaires for quality of life and symptoms
Time Frame: 5-7 months post hospital discharge for patients
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Dyspnoea-12 - min score 0 max score 36
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5-7 months post hospital discharge for patients
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questionnaires for quality of life and symptoms
Time Frame: 5-7 months post hospital discharge for patients
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Nottingham activities of daily living - min score 0 max score 22
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5-7 months post hospital discharge for patients
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questionnaires for quality of life and symptoms
Time Frame: 5-7 months post hospital discharge for patients
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Mental health assessed by personal health questionnaire - min score 0 max score 27
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5-7 months post hospital discharge for patients
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questionnaires for quality of life and symptoms
Time Frame: 5-7 months post hospital discharge for patients
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MoCA cognition level - min score 0 max score 30
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5-7 months post hospital discharge for patients
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questionnaires for quality of life and symptoms
Time Frame: 5-7 months post hospital discharge for patients
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Frailty as judged by Rockwood CFS - min score 1 max score 9
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5-7 months post hospital discharge for patients
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blood biomarkers for cardiac function
Time Frame: 5-7 months post hospital discharge for patients
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concentration of troponin
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5-7 months post hospital discharge for patients
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blood biomarkers for cardiac function
Time Frame: 5-7 months post hospital discharge for patients
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concentration of brain natriuretic peptide
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5-7 months post hospital discharge for patients
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blood biomarkers for renal function
Time Frame: 5-7 months post hospital discharge for patients
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calculated glomerular filtration rate
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5-7 months post hospital discharge for patients
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blood biomarkers for liver function
Time Frame: 5-7 months post hospital discharge for patients
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concentration of alanine transaminase
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5-7 months post hospital discharge for patients
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blood biomarkers for skeletal muscle function
Time Frame: 5-7 months post hospital discharge for patients
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concentration of creatine kinase
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5-7 months post hospital discharge for patients
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blood biomarkers for inflammation
Time Frame: 5-7 months post hospital discharge for patients
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concentration of cytokines such as TNF alpha, IL-6 and C-reactive peptide
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5-7 months post hospital discharge for patients
|
blood biomarkers for diabetes
Time Frame: 5-7 months post hospital discharge for patients
|
Measurement of HbA1c
|
5-7 months post hospital discharge for patients
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Charlotte E Bolton, Prof, NIHR Nottingham Biomedical Research Centre, Respiratory theme
Publications and helpful links
General Publications
- Bansal M. Cardiovascular disease and COVID-19. Diabetes Metab Syndr. 2020 May-Jun;14(3):247-250. doi: 10.1016/j.dsx.2020.03.013. Epub 2020 Mar 25.
- Docherty AB, Harrison EM, Green CA, Hardwick HE, Pius R, Norman L, Holden KA, Read JM, Dondelinger F, Carson G, Merson L, Lee J, Plotkin D, Sigfrid L, Halpin S, Jackson C, Gamble C, Horby PW, Nguyen-Van-Tam JS, Ho A, Russell CD, Dunning J, Openshaw PJ, Baillie JK, Semple MG; ISARIC4C investigators. Features of 20 133 UK patients in hospital with covid-19 using the ISARIC WHO Clinical Characterisation Protocol: prospective observational cohort study. BMJ. 2020 May 22;369:m1985. doi: 10.1136/bmj.m1985.
- Ronco C, Reis T, Husain-Syed F. Management of acute kidney injury in patients with COVID-19. Lancet Respir Med. 2020 Jul;8(7):738-742. doi: 10.1016/S2213-2600(20)30229-0. Epub 2020 May 14.
- Narici M, Vito G, Franchi M, Paoli A, Moro T, Marcolin G, Grassi B, Baldassarre G, Zuccarelli L, Biolo G, di Girolamo FG, Fiotti N, Dela F, Greenhaff P, Maganaris C. Impact of sedentarism due to the COVID-19 home confinement on neuromuscular, cardiovascular and metabolic health: Physiological and pathophysiological implications and recommendations for physical and nutritional countermeasures. Eur J Sport Sci. 2021 Apr;21(4):614-635. doi: 10.1080/17461391.2020.1761076. Epub 2020 May 12.
- Forster HV, Dempsey JA, Thomson J, Vidruk E, DoPico GA. Estimation of arterial PO2, PCO2, pH, and lactate from arterialized venous blood. J Appl Physiol. 1972 Jan;32(1):134-7. doi: 10.1152/jappl.1972.32.1.134. No abstract available.
- Piasecki M, Ireland A, Jones DA, McPhee JS. Age-dependent motor unit remodelling in human limb muscles. Biogerontology. 2016 Jun;17(3):485-96. doi: 10.1007/s10522-015-9627-3. Epub 2015 Dec 14.
- Meyerspeer M, Boesch C, Cameron D, Dezortova M, Forbes SC, Heerschap A, Jeneson JAL, Kan HE, Kent J, Layec G, Prompers JJ, Reyngoudt H, Sleigh A, Valkovic L, Kemp GJ; Experts' Working Group on 31P MR Spectroscopy of Skeletal Muscle. 31 P magnetic resonance spectroscopy in skeletal muscle: Experts' consensus recommendations. NMR Biomed. 2020 Feb 10;34(5):e4246. doi: 10.1002/nbm.4246. Online ahead of print.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 20050
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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