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. 2020 Jan 2;75(12):2361–2370. doi: 10.1093/gerona/glaa012

Table 1.

Participant Demographics and Impact of Parkinson’s Disease (n = 54)

Demographics Covariates n (range or %)
Age (years) 67.5 ± 6.3 (55–79)
Gender
 Men 38 (70.4%)
 Women 16 (29.6%)
Marital status
 Married/common law 45 (83.3%)
Income
 0–$19, 999 11 (20.4%)
 $20,000–$39,999 12 (22.2%)
 $40,000–$59,999 14 (25.9%)
 $60,000–$89,999 11 (20.4%)
 >$90,000 6 (11.1%)
Employment status Fully retired = 46 (85.2%)
Education
 < High school 11 (20.4%)
 High school graduate 11 (20.4%)
 Some college 3 (5.6%)
 College diploma 9 (16.7%)
 Undergraduate degree 8 (14.8%)
 Postgraduate program 1 (1.9%)
 Graduate degree 11 (20.4%)
Residential setting
 Urban 15 (27.8%)
 Suburban 11 (20.4%)
 Rural, in town 18 (33.3%)
 Rural, outside of town 10 (18.5%)
Living situation Cohabiting (with family/friends) = 45 (83.3%)
Driving status Drives 52 (96.3%)
Cognitive score (MoCA) 25.6 ± 2.7 (22–30)
Time since PD diagnosis (years) 6.2 ± 5.7 (0–30)
Impact of PD on dimensions of daily living (PDQ-39 scores): (0 = no impact, 100 = total impairment)
 1. Mobility 17.9 ± 20.9 (0–70.0)
 2. Activities of daily living 23.2 ± 18.4 (0–70.8)
 3. Emotional well being 19.1 ±16.6 (0–66.7)
 4. Perceived stigma 13.3 ± 16.0 (0–68.8)
 5. Social Support 8.3 ± 12.3 (0–50.0)
 6. Cognition 24.1 ± 19.3 (0–68.8)
 7. Communication 20.7 ± 19.0 (0–75.0)
 8. Bodily discomfort (eg, pain) 26.6 ±23.4 (0–100.0)
 9. Overall quality of life 19.1 ± 13.7 (1.8–64.7)

Note: Montreal COgnitive Assessment (MoCA) scores suggest some participants may have undetected mild cognitive impairment, even though it did not appear to affect their activities of daily living performance or performance on the orientation section of the MoCA. PD = Parkinson’s disease.