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Group Interventions for Cancer Patients
Ali and Khalil, found that a teaching session focused on concrete issues involved in surgical procedure (including a visit from someone who had previously undergone the procedure) was enough to help patients with bladder cancer cope with surgery. Sessions were less than one hour in length, and resulted in decreased anxiety up to the third postoperative day. Johnson, in his "I Can Cope" group sessions, extended the range of education to include such broader issues as coping with daily health concerns, communication, self-esteem, and living with limitations set by one's illness. Patients undergoing this intervention also reported decreased anxiety after the intervention, as compared with matched controls.
Many psychoeducational groups were modeled after the Omega Project, with its behavioral emphasis on teaching coping skills, including the use of illustrated problem cards to guide discussions. These interventions usually comprise approximately six sessions of one and one-half to two hours duration. They emphasize education, stress management, problem-solving, and support. The active coping style fostered by such groups has been found to be more beneficial to cancer patients than a passive or avoidant one. Participants in psychoeducational groups also have reported decreased psychological distress and better quality of life compared with controls.
Cain et al. compared individual and group methods of thematic counseling, and found no differences in their effectiveness for cancer patients, but found significantly improved coping for both groups compared with controls. Yalom, however, suggested that groups offer benefits not available in individual settings. These include a sense of universality among otherwise isolated people who may feel shunned because of their illness, a feeling of helping oneself by helping others, hopefulness fostered by seeing how others have coped successfully with difficult issues, and a general sense of belonging to a larger group. He developed a program of existential supportive-expressive group psychotherapy for women with metastatic breast cancer, which was also adapted by Spiegel and his colleagues. Groups had an unstructured open format, and generally met once weekly for one year, or, in some instances, two years. Special sessions were also included to teach relaxation and autohypnosis for pain. In addition to helping women deal with the disfiguring aspects of their illness, the authors' stated objective was to focus on living in the context of dying, and to foster patients' authentic processing of their situations.
Similar to the findings of the psychoeducational group research, Spiegel and his colleagues found that when the intervention ended, patients who had participated exhibited less distress in the form of tension, fatigue, and confusion, as well as less pain when compared with no-treatment control groups. While follow-up psychological measures were not taken, Spiegel found ten years later that group members also lived significantly longer than control subjects. This latter finding, however, has been the subject of some debate.
Kissane and colleagues combined aspects of Spiegel's model with a cognitive intervention for women in the earlier stages of breast cancer. Groups of six to eight patients met over a six-month period. Topics for discussion included grief work, coping skills, mastery, cognitive reframing, and the reordering of priorities. The authors suggest that their therapy is better suited for patients with early disease, for whom cure or survival is a realistic possibility, while groups with greater emphasis on existential issues and less on cognitive processes might be better suited to people with late-stage cancer. Edelman and colleagues applied a more purely cognitive model of group psychotherapy, with a focus on reframing irrational beliefs. However, they found this difficult, as many of the fears of cancer patients were not irrational but realistic, especially at later stages of disease.
Despite the relationship of a sense of meaningfulness to psychological well-being, meaning is not usually a focus of outcome research on cancer-patient psychotherapy groups. Rather, most of the outcome research tends to focus on symptom-based measures, particularly anxiety and depression, as well as measures of general mood states, such as the Profile of Mood States. There has been some criticism that empirical research has been hampered by too narrow a focus on the possible negative psychological sequelae of cancer without a concomitant discussion of the potential for positive psychological states as well. Indeed, in at least one study in which no differences between group members and control subjects were found on paper-and-pencil tests, clinical differences were observed by therapists. The authors suggest the possibility that these measures simply are not sensitive enough to the range of possible positive group outcomes.
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-Greenstein, Mindy & William Breitbart; Cancer and the experience of meaning: a group psychotherapy for people with cancer; American Journal of Psychotherapy; Fall 2000; Vol. 54; Issue 4.The article above contains foundational information. Articles below contain optional updates.
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