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. 2022 Sep 6;14(1):e12333. doi: 10.1002/dad2.12333

TABLE 1.

Participant characteristics

1. Needs survey 2. Focus groups 3. Validation survey
Phase Patients Care partners Patients Care partners Patients Care partners
N 50 a 46 7 7 28 b 12
Age, years 73 ± 8 c 65 ± 12 c 68 ± 6 70 ± 4 75 ± 7 c 69 ± 6 c
Female (%) 17 (41%) c 25 (60%) c 4 (57%) 4 (57%) 5 (18%) 3 (25%)
Education, years 11.8 ± 4.1 12.2 ± 4.4 12.3 ± 2.6 12.3 ± 2.6 12.3 ± 4.4 11.9 ± 4.1
Relation to patient, n (%)
Spouse N/A 33 (72%) N/A 6 (86%) N/A 12 (100%)
(Grand)child N/A 12 (26%) N/A 0 N/A 0
Sister/brother N/A 1 (2%) N/A 0 N/A 0
Other N/A 0 N/A 1 (14%) N/A 0

Diagnosis of patient, n (%) d

SCD 21 (42%) 2 (4%) 5 (71%) 2 (29%) 10 (36%) 0
MCI 16 (32%) 8 (17%) 2 (29%) 2 (29%) 11 (39%) 1 (8%)
Dementia 13 (26%) 36 (78%) 0 (0%) 3 (43%) 7 (25%) 11 (92%)

Note: Data represent mean ± SD or n (%). The groups of participants in phase 2 and phase 3 are subgroups of the participants from phase 1.

Abbreviations: MCI, mild cognitive impairment; N/A, not applicable; SD, standard deviation; SCD, subjective cognitive decline.

a

Of whom n = 20 (44%) participated together with their care partner.

b

Of whom n = 10 (36%) participated together with their care partner.

c

Pairwise comparisons indicate a group difference (P < .05).

d

Self‐reported data.