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Volume 53, Issue 1, Pages 47-55 (January 2000)


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Lessons learned from enrollment in the BEST study—A multicenter, randomized trial of group psychosocial support in metastatic breast cancer

Pamela J. GoodwinaCorresponding Author Informationemail address, Molyn Leszczb, Gail Quirtc, Jan Koopmansd, Andrew Arnolde, Elizabeth Dohanf, Marilyn Hundlebyg, Harvey Max Chochinovh, Margaret Navarroi

Received 5 May 1998; received in revised form 7 June 1999; accepted 13 July 1999.

Abstract 

The BEST study, a multicenter randomized trial of group psychosocial support in metastatic breast cancer, had several unusual features that may have influenced recruitment, notably the group nature of the intervention and the need for close collaboration between medical and psychosocial investigators. The recruitment process was examined in light of these features. Establishment of study centers was facilitated by involvement of experienced medical investigators who had successfully collaborated in previous research projects. Systematic evaluation of potential subjects or direct recruitment by psychosocial investigators optimized recruitment; however, the group nature of the intervention prolonged recruitment. Overall, 652 women were approached and 237 (43.3% of those medically eligible) randomized. Using population-based estimates, 24.3% of women with metastatic breast cancer were assessed for the study and 8.7% randomized. A randomization ratio of 2:1 was required to form and maintain groups. Competing clinical trials were the greatest barrier to recruitment. Five lessons were learned during recruitment for this trial: (1) multicenter randomized trials of psychosocial interventions are feasible, even in very ill patients, (2) the use of a group intervention effectively increased the required sample size by 50%, (3) similarity of randomization rates suggests that generalizability of study results will probably be comparable to that of other randomized cancer trials, (4) multidisciplinary collaborations and involvement of experienced researchers facilitated enrollment, and (5) most challenges encountered in recruitment were similar to those seen in all clinical trials.

a Department of Medicine, Division of Clinical Epidemiology, Clinical Epidemiology and Health Care Research Program, University of Toronto, Samuel Lunenfeld Research Institute, Mount Sinai Hospital, Toronto, Ontario, Canada

b Department of Psychiatry, Mount Sinai Hospital, University of Toronto, Toronto, Ontario, Canada

c Mount Sinai Hospital, Toronto, Ontario, Canada

d Department of Oncology, Tom Baker Cancer Center, University of Calgary, Calgary, Alberta, Canada

e Department of Medicine, Hamilton Regional Cancer Center, McMaster University, Hamilton, Ontario, Canada

f Department of Patient and Family Counseling, British Columbia Cancer Agency, University of British Columbia, Vancouver, British Columbia, Canada

g Department of Psychology, Cross Cancer Institute, University of Alberta, Edmonton, Alberta, Canada

h Department of Psychiatry, Department of Psychosocial Oncology, Manitoba Cancer Treatment and Research Foundation, University of Manitoba, Winnipeg, Manitoba, Canada

i Department of Psychiatry, Ottawa Regional Cancer Center, University of Ottawa, Ottawa, Ontario, Canada

Corresponding Author InformationCorresponding author. Tel.: 416-586-8605; Fax: 416-586-8659.(P.J. Goodwin)

PII: S0895-4356(99)00148-1


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