Thirty cancer out-patients, 28 out-patients with cardiac disease, and 24 controls matched for age, sex, race, religion, and marital status were administered a 38-item questionnaire on sleep habits. Patients with cardiac disease perceived that they had more difficulty falling asleep, awakened earlier than planned, and felt sleepy during the day more often than the other two groups. Patients with cancer differed from controls only in feeling that they had more difficulty staying asleep. The findings demonstrate that while patients with two different chronic diseases have altered sleep patterns, the patterns are disturbed in different ways. This has important implications for therapy as a different approach is needed for the patient who has difficulty falling asleep as compared with the patient who has difficulty staying asleep.
The degree of psychosocial distress experienced by 15 cancer patients with newly diagnosed metastatic disease and their spouses was investigated. Of interest were mean changes over the six-month interval following diagnosis, and correlations between partners at 0, 3, and 6-7 months. The Psychosocial Adjustment to Illness Scale (PAIS) and the Family Environment Scale (FES) were used to quantify adjustment. Several PAIS subscales exhibited increasing distress over time for patients: Social Environment (p = 0.004), Vocational Environment (p = 0.028), and Psychological Distress (p = 0.029). FES Conflict increased over time (p < 0.005), while Intellectual Cultural Orientation declined (p = 0.02), both for spouses only. Of 24 patient-spouse PAIS correlations (7 subscales plus a global scale, at three times), 7 (29%) were 0.70 or greater (ps < 0.01). Of 30 FES correlations, 17 (57%) were 0.7 or higher (ps < 0.01). These results suggest that some stresses increase over time, and that spouses and patients share a similar perceived level of distress. Health professionals must address the psychological distress of the spouse as well as the patient.
This study determined the factors influencing participation of elderly people in research. It involved subjects who signed consent for a study and those who refused consent. Consenters had significantly more positive feelings about being used as a subject; giving urine; giving blood; having a physical examination; being interviewed; taking an IQ test; answering questions; being a subject to help others; finding out about problems and as a way to pass time; and telling an interviewer the truth. Reasons given for partaking in research were the personality of the interviewer, interest in the project, and benefits to subject or others.
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