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. 2021 Dec 7;23(12):e21681. doi: 10.2196/21681

Table 1.

Characteristics of study participants who provided course-collected data and course completers who supplied feedback surveys. Please note that participants could select multiple MSa community rolesb.

Characteristic Course-collected data Feedback survey
Gender, n (%) 3492 (100) 1412 (100)

Male 552 (15.81) 227 (16.08)

Female 2940 (84.19) 1185 (83.92)
Education level, n (%) 2876 (100) 1549 (100)

No university education 1169 (40.65) 595 (38.41)

University education 1707 (59.35) 954 (61.59)
MS community rolesc, n (%) 3024 (100) 1549 (100)

Person with MS 928 (30.69) 437 (28.21)

Family member or friend 664 (21.96) 382 (24.66)

Carer 352 (11.64) 139 (8.97)

Service provider 360 (11.9) 92 (5.94)

Allied health 815 (26.95) 365 (23.56)

General practitioner 67 (2.22) 41 (2.65)

Neurologist 62 (2.05) 18 (1.16)

Advocate 67 (2.22) 44 (2.84)

Researcher 123 (4.07) 44 (2.84)

Other or no MS community role 374 (12.37) 321 (20.72)
Country of residence, n (%) 3509 (100) 1417 (100)

Australia 2180 (62.13) 907 (64.01)

Canada 100 (2.85) 38 (2.68)

United Kingdom 255 (7.27) 101 (7.13)

Ireland 133 (3.79) 44 (3.11)

New Zealand 277 (7.89) 127 (8.72)

United States 106 (3.02) 35 (2.47)

South Africa 51 (1.45) 27 (1.91)

Other 407 (11.6) 138 (9.74)
Final section completed, n (%) 3518 (100) d

<Module 1 620 (17.62)

Module 1 251 (7.13)

Module 2 90 (2.59)

Module 3 74 (2.1)

Module 4 72 (2.05)

Module 5 48 (1.36)

Module 6 2363 (67.17)
Age (years), mean (SD) 44.38 (13.34)e 46.78 (13.10)f
Disease duration (years), median (SD) 4 (10) 5 (10)g

aMS: multiple sclerosis.

bAmong people with multiple sclerosis, approximately half of the participants who provided course-collected data and those who provided feedback data had a disease duration of 4 years or less. Consequently, the distribution was highly skewed toward 0 years (diagnosis in 2019; Multimedia Appendix 1).

cMultiple selections possible.

dNot available.

eN=3292.

fN=1330.

gN=401.