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Spots Global Cancer Trial Database for Group Therapy Compared With Educational Materials in Patients With Prostate Cancer

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We do not endorse or review these studies in any way.

Trial Identification

Brief Title: Group Therapy Compared With Educational Materials in Patients With Prostate Cancer

Official Title: SUPPORTIVE-EXPRESSIVE GROUP THERAPY FOR MEN WITH PRIMARY PROSTATE CANCER

Study ID: NCT00002848

Study Description

Brief Summary: RATIONALE: Developing coping strategies may help improve the quality of life of patients with prostate cancer. PURPOSE: This randomized clinical trial is comparing the effect of group therapy with written educational materials on the quality of life of men with stage I or stage II prostate cancer.

Detailed Description: OBJECTIVES: * Determine the feasibility of providing group support, and evaluate the effect of supportive-expressive group therapy vs. written educational material on the psychological health and quality of life of men with stage I/II prostate cancer. OUTLINE: Patients are stratified by prior hormonal therapy. Patients continue standard oncologic treatment concurrently with supportive-expressive group therapy. Supportive-expressive group therapy consists of twelve 90-minute weekly meetings with 8-12 members and 2 cotherapists and is based on the following themes: building bonds, expressing emotions, detoxifying dying, taking time to prioritize and set realistic goals, fortifying families, and dealing with doctors. Each session commences with a brief stress reduction exercise and ends with a brief cognitive restructuring imagery exercise. The main portion of the meeting emphasizes providing an environment in which patients can share their concerns, feelings, and thoughts openly and honestly. The role of the cotherapist is to facilitate expression of patients' concerns, offer empathy, and continue to encourage patients to express their feelings and thoughts. Quality-of-life questionnaires are filled out at 3 and 6 months and then every 6 months for a total of 2 years. PROJECTED ACCRUAL: Approximately 480 patients (including an estimated 53 minority patients) will be entered in this multicenter study.

Eligibility

Minimum Age:

Eligible Ages: CHILD, ADULT, OLDER_ADULT

Sex: MALE

Healthy Volunteers: No

Locations

CCOP - Western Regional, Arizona, Phoenix, Arizona, United States

Stanford Cancer Center at Stanford University Medical Center, Stanford, California, United States

CCOP - Wichita, Wichita, Kansas, United States

CCOP - Kalamazoo, Kalamazoo, Michigan, United States

James P. Wilmot Cancer Center at University of Rochester Medical Center, Rochester, New York, United States

CCOP - Columbus, Columbus, Ohio, United States

CCOP - Northwest, Tacoma, Washington, United States

Contact Details

Name: Gary R. Morrow, PhD, MS

Affiliation: James P. Wilmot Cancer Center

Role: STUDY_CHAIR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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