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Re-hospitalization (infection-related and all-cause)
Time frame: 30 days after discharge; 180 days after discharge.
Report of the total number of re-hospitalized patients, defined as a hospital stay >12 hours.
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Mortality (infection-related and all-cause)
Time frame: 30 days after discharge; 90 days after discharge; 180 days after discharge; 360 days after discharge
Report of the total number.
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Handgrip strength
Time frame: Baseline; 1-month after discharge (secondary endpoint); 3-month after discharge (primary endpoint); and 6-month after discharge (secondary endpoint).
Measure handgrip muscle strength in kilos in the dominant hand using a hand-held dynamometer. The highest number out of three attempts will be recorded.
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Lower limb muscle strength and power
Time frame: Baseline; 1-month after discharge (secondary endpoint), 3-month after discharge (primary endpoint), and 6-month after discharge (secondary endpoint).
Assessment of muscle strength and power of the knee extensor muscles with dynamometry.
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30-second sit to stand
Time frame: Baseline; 1-month after discharge (secondary endpoint); 3-month after discharge (primary endpoint); and 6-month after discharge (secondary endpoint).
A clinical test where the patient performs as many sit-to-stand actions as possible in 30 seconds. Measures leg muscle strength by counting the number of repetitions.
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1-minute sit to stand
Time frame: Baseline; 1-month after discharge (secondary endpoint); 3-month after discharge (primary endpoint); and 6-month after discharge (secondary endpoint).
A clinical test where the patient performs as many sit-to-stand actions as possible in 1 minute. Measures endurance by counting the number of repetitions.
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6-minute walking test
Time frame: Baseline; 1-month after discharge (secondary endpoint); 3-month after discharge (primary endpoint); and 6-month after discharge (secondary endpoint).
Measure the distance in meters a person can walk in 6 minutes.
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Short Physical Performance Battery (SPPB)
Time frame: Baseline; 1-month after discharge (secondary endpoint); 3-month after discharge (primary endpoint); and 6-month after discharge (secondary endpoint).
An objective measurement instrument combining 3 tests in 1 score. The tests consist of a balance test (measured in seconds), lower extremity strength (measured in seconds), and a walking test measuring functional capacity (measured in seconds).
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Barthel index
Time frame: Baseline; 1-month after discharge (secondary endpoint); 3-month after discharge (primary endpoint); and 6-month after discharge (secondary endpoint).
Measure of a persons ability to perform activities of daily living. Scores from 0 to 100. The higher the better.
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Clinically Frailty Scale
Time frame: Baseline; 1-month after discharge (secondary endpoint); 3-month after discharge (primary endpoint); and 6-month after discharge (secondary endpoint).
A global clinical measure of the overall frailty of an older person. Scores from 1 to 9. The lower the better.
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EuroQol-5D-5L (EQ-5D-5L)
Time frame: Baseline; 1-month after discharge (secondary endpoint); 3-month after discharge (primary endpoint); and 6-month after discharge (secondary endpoint).
Measure health-related quality of life divided into the EQ-5D utility index and EQ-VAS score. The Danish EQ-5D-5L utility scores range from -0.757 for state 55555 to 1.0 for state 11111; the higher the score, the better. The EQ VAS is on a 0-100 scale; the higher the score, the better.
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36-Item Short Form Survey (SF-36)
Time frame: Baseline; 1-month after discharge (secondary endpoint); 3-month after discharge (primary endpoint); and 6-month after discharge (secondary endpoint).
Measure health-related quality of life. Total score from 0 to 100; the higher the score, the better.
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COPD Assessment Test (CAT)
Time frame: Baseline; 1-month after discharge (secondary endpoint); 3-month after discharge (primary endpoint); and 6-month after discharge (secondary endpoint).
A patient self-administered questionnaire. An 8-item questionnaire designed to assess the impact of disease on a person's life (health status). Range of CAT scores from 0-40. Higher scores implicates a more severe impact of COPD on a patient's life (total score point).
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Montreal Cognitive Assessment (MoCA)
Time frame: Baseline; 1-month after discharge (secondary endpoint); 3-month after discharge (primary endpoint); and 6-month after discharge (secondary endpoint).
Measure of mild cognitive impairment. MoCa scores range from 0 to 30. Scores of 26 or over are considered to be normal.
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Center for Epidemiologic Studies Depression Scale (CES-D)
Time frame: Baseline; 1-month after discharge (secondary endpoint); 3-month after discharge (primary endpoint); 6-month after discharge (secondary endpoint)
A self-report rating scale that is designed to measure current symptoms of depression. Lower score is better.
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Family Reported Outcome Measure (FROM-16)
Time frame: 1-month after discharge (secondary endpoint); 3-month after discharge (primary endpoint); 6-month after discharge (secondary endpoint)
Measure of the impact on the quality of life of an adult family member or partner resulting from having a person (of any age) in a family with any disease or condition, across all of medicine.
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Physical activity level
Time frame: Baseline; 1-month after discharge (secondary endpoint); 3-month after discharge (primary endpoint); 6-month after discharge (secondary endpoint)
The objectivly measured physical activity level assessed with activity trackers.
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Blood sample
Time frame: Baseline; discharge (secondary endpoint); 1-month after discharge (seconary endpoint), 3-month after discharge (primary endpoint), 6-month after discharge (secondary endpoint), and 12-month after discharge (secondary endpoint).
Concentration of p-phosphate (mmol/l), p-sodium (mmol/l), p-carbamide (mmol/l), and p-potassium (mmol/l).
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Blood sample
Time frame: Baseline; discharge (secondary endpoint); 1-month after discharge (seconary endpoint), 3-month after discharge (primary endpoint), 6-month after discharge (secondary endpoint), and 12-month after discharge (secondary endpoint).
Concentration of pro- and anti-inflammatory cytokines (IL-6, Il-1ra, IL-18, IL-10, TNF-alpha, etc.)
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Blood sample
Time frame: Baseline; discharge (secondary endpoint); 1-month after discharge (seconary endpoint), 3-month after discharge (primary endpoint), 6-month after discharge (secondary endpoint), and 12-month after discharge (secondary endpoint).
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Blood sample
Time frame: Baseline; discharge (secondary endpoint); 1-month after discharge (seconary endpoint), 3-month after discharge (primary endpoint), 6-month after discharge (secondary endpoint), and 12-month after discharge (secondary endpoint).
Concentration of galectin-3 (ng/ml), sST2 (ng/ml), and troponins (ng/ml).
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Blood sample
Time frame: Baseline; discharge (secondary endpoint); 1-month after discharge (seconary endpoint), 3-month after discharge (primary endpoint), 6-month after discharge (secondary endpoint), and 12-month after discharge (secondary endpoint).
Concentration of NT-proBNP (ng/l).
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Immune function
Time frame: Baseline; discharge (secondary endpoint); 1-month after discharge (seconary endpoint), 3-month after discharge (primary endpoint), 6-month after discharge (secondary endpoint), and 12-month after discharge (secondary endpoint).
Complete blood count with differential count. Concentration of immunoglobulin G (IgG), immunoglobulin M (IgM), and immunoglobulin A (IgA), and concentration of subclasses of IgG: IgG1, IgG2, IgG3, and IgG4.
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Blood sample
Time frame: Baseline; discharge (secondary endpoint); 1-month after discharge (seconary endpoint), 3-month after discharge (primary endpoint), 6-month after discharge (secondary endpoint), and 12-month after discharge (secondary endpoint).
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Blood sample
Time frame: Baseline; 1-month after discharge (secondary endpoint); 3-month after discharge (primary endpoint); 6-month after discharge (secondary endpoint); and 12-month after discharge (secondary endpoint).
Concentration of c-peptide (pmol/L).
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Blood sample
Time frame: Baseline; 1-month after discharge (secondary endpoint); 3-month after discharge (primary endpoint); 6-month after discharge (secondary endpoint); and 12-month after discharge (secondary endpoint).
Concentration p-glucose (mmol/L).
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Blood sample
Time frame: Baseline; 1-month after discharge (secondary endpoint); 3-month after discharge (primary endpoint); 6-month after discharge (secondary endpoint); and 12-month after discharge (secondary endpoint).
Concentration of p-insulin (pmol/L).
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Biobank blood sample
Time frame: Baseline; discharge (secondary endpoint); 1-month after discharge (seconary endpoint), 3-month after discharge (primary endpoint), 6-month after discharge (secondary endpoint), and 12-month after discharge (secondary endpoint).
Whole blood, plasma, and serum.
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Insulin resistance
Time frame: Baseline; 1-month after discharge (secondary endpoint); 3-month after discharge (primary endpoint), and 6-month after discharge (secondary endpoint).
The Homeostatic Model Assessment for Insulin Resistance (HOMA-IR) will be used to measure severity of insulin resistance. Normal reference levels for HOMA-IR is 0.7 to 2.0, with values >2.0 representing clinically significant insulin resistance.
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Glycemic variability
Time frame: Baseline (day 0-10); 3-month after discharge (day 80-90, primary endpoint), and 6-month after discharge (day 170-180, secondary endpoint).
Glucose outcomes from the CGM sensor (Dexcom G6) including time in range (TIR) for blood glucose, time above range (TAR) for blood glucose, time below range (TBR) for blood glucose, average blood glucose, and variance in blood glucose (CV).
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P-glucose during an oral glucose tolerance test (OGTT)
Time frame: Baseline; 3-month after discharge (primary endpoint), and 6-month after discharge (secondary endpoint).
P-glucose (mmol/L) measured during an OGTT.
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P-insulin during an oral glucose tolerance test (OGTT)
Time frame: Baseline; 3-month after discharge (primary endpoint), and 6-month after discharge (secondary endpoint).
P-insulin (pmol/L) measured during an OGTT.
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C-peptide during an oral glucose tolerance test (OGTT)
Time frame: Baseline; 3-month after discharge (primary endpoint), and 6-month after discharge (secondary endpoint).
C-peptide (pmol/L) measured during an OGTT.
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Insulin sensitivity
Time frame: Baseline; 3 month after discharge (primary endpoint); 6 months after discharge (secondary endpoint).
Insulin sensitivity using Matsuda index. The index is calculated based on p-glucose and p-insulin in fasting state and during an OGTT.
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Glucose-lowering medication
Time frame: Baseline; 3 months after discharge (primary endpoint); 6 months after discharge (secondary endpoint)
Changes in glucose-lowering medication in patients with diabetes
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Semi-structured qualitative interviews
Time frame: 1-month after discharge (seconary endpoint), 3-month after discharge (primary endpoint), and 6-month after discharge (secondary endpoint).
Semi-structured qualitative interviews with the patient and a relative. The following themes will be explored: perception of the content in the exercise intervention, barriers and enablers towards physical activity, ideas for improvement of the exercise intervention
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Adverse events
Time frame: At 1-month after discharge, 3-month after discharge (primary endpoint), and 6-month after discharge.
Numbers of severe adverse events and adverse events
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Total and appendicular lean and fat mass
Time frame: Baseline; 1-month after discharge (secondary endpoint); 3-month after discharge (primary endpoint); and 6-month after discharge (secondary endpoint).
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Muslce quality and density
Time frame: Baseline; 3-month after discharge (primary endpoint); and 6-month after discharge (secondary endpoint).
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Fat mass index and fat-free mass index
Time frame: Baseline; 1-month after discharge (secondary endpoint); 3-month after discharge (primary endpoint); and 6-month after discharge (secondary endpoint).
Bioelectrical impedance analysis
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Muscle oxidative stress and inflammation
Time frame: Baseline; 3-month after discharge (primary endpoint); and 6-month after discharge (secondary endpoint).
Muscle biopsies from the m. vastus lateralis of the quadriceps muscle
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Muscle protein synthesis and proteolysis
Time frame: Baseline; 3-month after discharge (primary endpoint); and 6-month after discharge (secondary endpoint).
Muscle biopsies from the m. vastus lateralis of the quadriceps muscle
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Muscle insulin sensitivity
Time frame: Baseline; 3-month after discharge (primary endpoint); and 6-month after discharge (secondary endpoint).
Muscle biopsies from the m. vastus lateralis of the quadriceps muscle
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Skeletal muscle cell growth, development, and function
Time frame: Baseline; 3-month after discharge (primary endpoint); and 6-month after discharge (secondary endpoint)
Skeletal muscle cell cultures of muscle tissue from m. vastus lateralis of the quadriceps muscle.
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Insulin sensitivity and signaling of adipose tissue
Time frame: Baseline; 3-month after discharge (primary endpoint); and 6-month after discharge (secondary endpoint)
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Adipose tissue inflammation
Time frame: Baseline; 3-month after discharge (primary endpoint); and 6-month after discharge (seconary endpoint)
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Adipose tissue immune cell infiltration
Time frame: Baseline; 3-month after discharg (primary endpoint); and 6-month after discharge (secondary endpoint)
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Pulmonary medication
Time frame: Baseline; 3 months after discharge (primary endpoint); 6 months after discharge (secondary endpoint)
Changes in pulmonary medication (tablets and inhalation)
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Lung function
Time frame: Baseline; 3 months after discharge (primary endpoint); 6 months after discharge (secondary endpoint)
Spirometry in patients with COPD
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Lung function
Time frame: Baseline; 3 months after discharge (primary endpoint); 6 months after discharge (secondary endpoint)
Body plethysmography in patients with COPD
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Lung function
Time frame: Baseline, 3 months after discharge (primary endpoint); 6 months after discharge (seconary endpoint)
Single-breath carbon monoxide uptake in patients with COPD
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Acute exacerbations of COPD
Time frame: Baseline; 3 months after discharge (primary endpoint); 6 months after discharge (secondary endpoint)
Notification of acute exacerbations of COPD through patient files
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Health economics
Time frame: From baseline to 360 days after discharge.
Health costs, the cost per quality-adjusted life years (QALYs), and the lifetime estimated cost per QALY gained will be calculated.