Table 1.
Cohorts | Trial design | Domains assessed | Domains assessed digitally | |
---|---|---|---|---|
RADAR-AD | HC n = 70 PreAD n = 38 ProAD, n = 65 MildAD n = 56 |
8 W observation period |
|
|
Mobilise-D | PD n = 600 MS n = 600 COPD n = 600 PFF n = 600 |
1 W observation period every 6 M (5 times in total per participant) |
|
|
IDEA-FAST | HC n = 200 PD n = 500 IBD n = 500 RA n = 200 SLE n = 200 PSS n = 200 |
1 W observation period every 6 W (4 times in total per participant) |
|
|
AD, Alzheimer’s disease; BIA, body impedance analysis; COPD, Chronic Obstructive Pulmonary Disease; ECG, electrocardiography; EEG, electroencephalography; HC, healthy controls; IBD, Inflammatory bowel disease; IMU, inertial measurement unit; M, months; MildAD, mild-to-moderate AD (dementia, Aβ-positive); MS, multiple Sclerosis; PD, Parkinson’s disease; PFF, Proximal Femur Fracture; preAD, preclinical AD (cognitively normal, Aβ-positive); proAD, prodromal AD (mild cognitive impairment, Aβ-positive); PSS, Primary Sjogren’s syndrome; RA, Rheumatoid Arthritis; SLE, Systemic Lupus Erythematosus; SS; supervised setting; TUG, timed up and go test; US unsupervised setting; W, week(s); 6MWT, 6 min walking test.