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Affect of Advertisements on Treatment Compliance in Women With Breast Cancer
This study is ongoing, but not recruiting participants.
Sponsored by: Institut Bergonie
Information provided by: National Cancer Institute (NCI)
ClinicalTrials.gov Identifier: NCT00462410
  Purpose

RATIONALE: Measuring how advertising affects treatment compliance in women with breast cancer may help doctors plan the best treatment.

PURPOSE: This clinical trial is studying how advertisements affect treatment compliance in women with breast cancer.


Condition Intervention
Breast Cancer
Procedure: counseling
Procedure: psychosocial assessment and care

Genetics Home Reference related topics: breast cancer
MedlinePlus related topics: Breast Cancer Cancer
U.S. FDA Resources
Study Type: Interventional
Study Design: Health Services Research, Open Label
Official Title: Socio-Anthropological Study Evaluating the Impact of Observance or Treatment in Patients With Breast Cancer

Further study details as provided by National Cancer Institute (NCI):

Primary Outcome Measures:
  • Treatment compliance [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • Factors affecting adherence to the medical plan [ Designated as safety issue: No ]

Estimated Enrollment: 65
Study Start Date: March 2006
Detailed Description:

OBJECTIVES:

Primary

  • Evaluate the consequences of advertisement on treatment compliance in women with breast cancer.

Secondary

  • Determine the factors favoring or not favoring adherence to the medical recommendations.

OUTLINE: Patients and their medical and nonmedical caregivers are interviewed by a sociologist or anthropologist twice over 1 year. The first interview is at the consultation visit and the second interview is at the patient's home. The impact of advertisement on treatment compliance is measured.

PROJECTED ACCRUAL: A total of 65 patients will be accrued for this study.

  Eligibility

Genders Eligible for Study:   Female
Accepts Healthy Volunteers:   No
Criteria

DISEASE CHARACTERISTICS:

  • Diagnosis of breast cancer
  • Hormone receptor status not specified

PATIENT CHARACTERISTICS:

  • Female
  • Menopausal status not specified

PRIOR CONCURRENT THERAPY:

  • Not specified
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00462410

Sponsors and Collaborators
Institut Bergonie
Investigators
Study Chair: Marc Debled, MD Institut Bergonie
  More Information

Clinical trial summary from the National Cancer Institute's PDQ® database  This link exits the ClinicalTrials.gov site

Study ID Numbers: CDR0000540528, IB-2006-03, INCA-REF0145, INCA-SOCIO-ANTHROPO
Study First Received: April 18, 2007
Last Updated: July 23, 2008
ClinicalTrials.gov Identifier: NCT00462410  
Health Authority: United States: Federal Government

Keywords provided by National Cancer Institute (NCI):
recurrent breast cancer
stage I breast cancer
stage II breast cancer
stage IIIA breast cancer
stage IIIB breast cancer
stage IIIC breast cancer
stage IV breast cancer

Study placed in the following topic categories:
Skin Diseases
Breast Neoplasms
Breast Diseases
Recurrence

Additional relevant MeSH terms:
Neoplasms
Neoplasms by Site

ClinicalTrials.gov processed this record on January 16, 2009