Feasibility of a Supportive Education Program for Latina Breast Cancer Survivors

City of Hope

Status: Terminated

Conditions: Stage IIIA Breast Cancer; Stage IIIB Breast Cancer; Stage IIIC Breast Cancer; Stage II Breast Cancer; Stage I Breast Cancer; Cancer Survivor

Treatments: Other: Educational Intervention

Study type: Interventional

Funder types: Other

Identifiers

NCT01628887

12175

Details and patient eligibility

About

This clinical trial studies a supportive education program for Latina breast cancer survivors. The Bilingual Breast Cancer Education Intervention (BBCEI) may help Latina breast cancer survivors know what to expect after completing breast cancer treatment and prepare them to cope with cancer related survivorship issues

Full description

PRIMARY OBJECTIVES: I. Describe the feasibility of implementing the BBCEI. II. Describe the cultural and linguistic appropriateness of the BBCEI. III. Determine topics requiring further emphasis in the BBCEI. IV. Identify ways to enhance program content, format, and materials. OUTLINE: Participants undergo 2 tailored BBCEI sessions within 1 month. At the beginning of the first session the research nurse will present the participants with a list of common physical and social concerns. The participant will then be asked to identify 3 topics that she wants to discuss. The research nurse will discuss with the participant any relevant supportive care resources and make the appropriate referrals. At the second session the focus of the BBCEI will be on psychological and spiritual well-being.

Enrollment: 4 patients

Sex: Female

Ages: 21+ years old

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

The population will consist of Latinas with breast cancer who have completed primary cancer treatment. A total of 10 subjects will be accrued.

Inclusion Criteria:

• Diagnosis of Stage I, II or III.
• Self-identification as Hispanic/Latina.
• Able to read and understand English or Spanish to participate in the education sessions.
• Ability to read and/or understand the study protocol requirements, and provide written informed consent
• Subjects maybe be on hormonal therapy after treatment for initial breast cancer.

Exclusion Criteria:

• Actively receiving treatment with surgery, radiation therapy, or chemotherapy.
• Patients who have recurrence, metastasis, or a second primary cancer

Trial design

Primary purpose: Supportive Care

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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4 participants in 1 patient group

Supportive Care (BBCEI)

Experimental group

Description:

Participants undergo 2 tailored BBCEI sessions within 1 month. At the beginning of the first session the research nurse will present the participants with a list of common physical and social concerns. The participant will then be asked to identify 3 topics that she wants to discuss. The research nurse will discuss with the participant any relevant supportive care resources and make the appropriate referrals. At the second session the focus of the BBCEI will be on psychological and spiritual well-being.

Treatment:

Other: Educational Intervention