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. Author manuscript; available in PMC: 2015 Oct 1.
Published in final edited form as: J Pain Symptom Manage. 2014 Apr 21;48(4):558–568. doi: 10.1016/j.jpainsymman.2013.10.025

Table 1.

Demographic/Clinical Characteristics of the Sample (N = 276)

Variables Number of patients (%)
Data collection sitea Site A 152 (55.1)
Site B 87 (31.5)
Others 37 (13.4)
Age (mean years ± SD) 53.97 (±11.79)
Gender Female 228 (82.6)
Male 48 (17.4)
Marital status Married 191 (69.2)
Single 81 (29.4)
Missing 4 (1.4)
Race Caucasian 242 (87.7)
Non-Caucasian 30 (10.9)
Missing 4 (1.4)
Education High school or less 70 (25.4)
Post-high school education 201 (72.8)
Missing 5 (1.8)
Employment status Employed 150 (54.3)
Unemployed 122 (44.2)
Missing 4 (1.5)
Study Groupb Experimental group 142 (51.4)
Control group 134 (48.6)
Cancer Type Breast 152 (55.1)
Lung 47 (17.0)
Gynaecologic cancer 32 (11.6)
Lymphoma 23 (8.3)
Others 22 (8.0)
Disease stage Stage 1 44 (15.9)
Stage 2 90 (32.6)
Stage 3 68 (24.6)
Stage 4 44 (15.9)
Not staged 30 (10.9)
Time lapse since the first CTX 43–46 vs. 159(57.6)
57–60 day 111(40.2)
Missing 6 (2.2)
Surgery right before baseline Yes 198 (71.7)
No 75 (27.2)
Missing 3 (1.1)
Treatment modality during the study CTX only 250 (90.6)
Concurrent treatment with radiation treatment 18 (6.5)
Missing 8 (2.9)
Comorbid conditions Hypertension 69 (25.0)
Arthritis 28 (10.1)
Hemoglobin at Time 1 12.92 (±1.6)
Hemoglobin at Time 2 11.75 (±1.6)

Note.

a

Site A= Fox Chase Cancer Center, Site B= Utah.

b

The primary study was a randomized clinical trial of the effectiveness of a cognitive-behavioral intervention on fatigue and insomnia.