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. 2014 May 1;23(5):420–427. doi: 10.1089/jwh.2013.4516

Table 1.

Baseline Demographic and Health Characteristics Among 1,261 Participants

  Total n (%)*
Race/ethnicity
 Non-Latina white 441 (35.0%)
 Latina 301 (23.9%)
 Black or African American 281 (22.2%)
 Asian/Pacific Islander 238 (18.9%)
Age at survey
 40–50 379 (30.0%)
 51–65 668 (53.0%)
 65–74 214 (17.0%)
Marital status
 Married/living with partner 565 (45.1%)
 Other 688 (54.9%)
Education
 High school diploma or less 405 (32.4%)
 Some college 322 (25.8%)
 College graduate or more 522 (41.8%)
Employment status
 Full time 340 (27.0%)
 Part time 244 (19.4%)
 Retired 219 (17.4%)
 Not working 455 (36.2%)
Insurance
 Private insurance 603 (47.8%)
 Public insurance 625 (49.6%)
 No insurance 33 (2.6%)
Language of interview
 English 1,098 (87.1%)
 Spanish or Cantonese 163 (12.9%)
Clinic site
 Site 1 (academic) 865 (68.6%)
 Site 2 (safety net) 396 (31.4%)
Randomization group
 Intervention 596 (47.2%)
 Comparison 665 (52.8%)
Number of comorbid conditions
 0 86 (6.8%)
 1–2 504 (40.0%)
 3 or more 671 (53.2%)
Number of primary care visits in last year
 0–1 357 (28.7%)
 2–3 429 (34.4%)
 4+ 460 (36.9%)
Self-perceived general health
 Excellent/very good 426 (34.0%)
 Good/fair/poor 828 (66.0%)
Breast cancer risk
 High risk – Gail/BCSC 202 (16.0%)
 High risk – RST 112 (8.9%)
 Average risk – relatives with BC 179 (14.2%)
 Average risk – no relatives with BC 768 (60.9%)
*

Percentages based on non-missing values.

BC, breast cancer; BCSC, Breast Cancer Surveillance Consortium Model; RST, referral screening tool.