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Survivorship Plans and Outcomes in Underserved Breast Cancer Survivors RCT


N/A
21 Years
N/A
Not Enrolling
Female
Breast Cancer

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Trial Information

Survivorship Plans and Outcomes in Underserved Breast Cancer Survivors RCT


Inclusion Criteria:



- Female

- 21 years of age or older

- English- or Spanish-speaking

- Diagnosis of ductal carcinoma in situ (DCIS) or Stage I, II, or III BC for the first
time

- 12 months post-diagnosis

- At least 1 month post-chemotherapy completion

Exclusion Criteria:

- Previous cancer except non-melanomatous skin cancers or in situ non-breast cancers

- Pregnant and lactating women

- Patients receiving parenteral anti-cancer therapy, except trastuzumab

- Clinically apparent cognitive or psychiatric impairment

- Participation in another research study

- Current treatment for another cancer

- Male

Type of Study:

Interventional

Study Design:

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Health Services Research

Outcome Measure:

Provider Adherence Score (PAS)

Outcome Description:

Discussion and implementation of recommended breast cancer (BC) survivorship care, including surveillance and the evaluation and management of BC treatment-related symptoms, bone health, weight, vasomotor symptoms, mammography, clinical breast examinations, and depression, as well as discussion of the patient's primary BC-related concern.

Outcome Time Frame:

One year post-intervention

Safety Issue:

No

Principal Investigator

Rose C Maly, MD, MSPH

Investigator Role:

Principal Investigator

Investigator Affiliation:

University of California, Los Angeles

Authority:

United States: Institutional Review Board

Study ID:

1R01CA140481

NCT ID:

NCT01627366

Start Date:

August 2012

Completion Date:

September 2015

Related Keywords:

  • Breast Cancer
  • Breast Neoplasms

Name

Location

UCLALos Angeles, California  90095