Ethnic Differences in the Impact of Breast Cancer on Employment Status, Financial Situation, and Quality of Life
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Purpose
The purpose of this study is to learn more about how being treated for breast cancer affects patients' employment, financial situation, and quality of life on a short-term basis and on a longterm basis. Most studies of employment after breast cancer have focused on Caucasian women.This study will evaluate the impact of breast cancer on the lives of women from different ethnic groups.
| Condition | Intervention |
|---|---|
|
Breast Cancer |
Behavioral: survey web-based or telephone interview |
| Study Type: | Observational |
| Study Design: | Observational Model: Case Control Time Perspective: Prospective |
| Official Title: | Breast Cancer and the Workforce: Ethnic Differences in the Impact of Breast Cancer on Employment Status, Financial Situation, and Quality of Life (BCW) |
- To compare the impact of breast cancer on (a) employment status, (b) financial situation, and (c) QoL. [ Time Frame: 3 years ] [ Designated as safety issue: No ]
- To identify barriers to employment and correlates of employment status, financial situation, and QoL. [ Time Frame: 3 years ] [ Designated as safety issue: No ]
- To develop the methodology to evaluate discrimination in the labor market using a validated instrument and to determine whether or not labor market discrimination is exacerbated by a diagnosis of breast cancer. [ Time Frame: 3 years ] [ Designated as safety issue: No ]
| Estimated Enrollment: | 750 |
| Study Start Date: | May 2010 |
| Estimated Study Completion Date: | May 2013 |
| Estimated Primary Completion Date: | May 2013 (Final data collection date for primary outcome measure) |
| Groups/Cohorts | Assigned Interventions |
|---|---|
|
Breast cancer survivors
Women being treated for stage I-III breast cancer who were employed prior to this diagnosis will be recruited in their physicians' offices.
|
Behavioral: survey web-based or telephone interview
Patients will be asked to complete a questionnaire at baseline, and then one at follow up, 3-4 months after treatment completion. The patient will be contacted one and two years after the completion of their follow up questionnaire for a brief one-question survey regarding current employment status.
|
|
Comparison group
Peer controls will be nominated by participants in the breast cancer survivor group or recruited by community outreach and matched for age, language, and ethnicity.
|
Behavioral: survey web-based or telephone interview
Patients will be asked to complete a questionnaire at baseline, and then one at follow up, 3-4 months after treatment completion.
|
Eligibility| Ages Eligible for Study: | 18 Years to 64 Years |
| Genders Eligible for Study: | Female |
| Accepts Healthy Volunteers: | Yes |
| Sampling Method: | Non-Probability Sample |
We will recruit participants from Memorial Sloan-Kettering Cancer Center (MSKCC), four of its community-based outpatient treatment centers, and six urban community hospitals that serve large populations of ethnic minorities in New York City. The MSKCC outpatient regional sites are located in New Jersey (Basking Ridge) and New York, with two in Long Island (Commack and Rockville Centre) and another in Westchester County (Sleepy Hollow).
Inclusion Criteria:
Breast cancer survivors
- Pathologic diagnosis of stage I-III breast cancer
- Paid employment (full time or part time) at time of consent or in the three months prior to diagnosis
- Age 18 to 64 years (inclusive)
- The ability to give informed consent in Chinese (Mandarin), English, Korean, or Spanish. At Lincoln Medical and Mental Health Center, patients must be able to give consent in English or Spanish. At Bellevue Hospital Center and Woodhull Medical and Mental Health Center patients must be able to give consent in Chinese, English or Spanish.
Comparison group
Paid employment (full time or part time) at the time of consent
- Age 18 to 64 years (inclusive) and within an age range that is 5 years above or below that of the nominating or matched survivor
- The ability to give informed consent in the same language as the nominating survivor
- Membership in the same ethnic group as the nominating survivor
- Not treated for cancer in the past year (other than non-melanoma skin cancer)
Exclusion Criteria:
- N/A
Contacts and Locations| Contact: Victoria Blinder, M.D., M.Sc. | 646-888-4808 | |
| Contact: Francesca Gany, M.D., M.Sc. | 646-888-4240 |
| United States, New Jersey | |
| Memoral Sloan Kettering Cancer Center | Recruiting |
| Basking Ridge, New Jersey, United States | |
| Contact: Victoria Blinder, M.D., M.Sc 646-888-4808 | |
| United States, New York | |
| Woodhull Medical and Mental Health Center | Suspended |
| Brooklyn, New York, United States, 11206 | |
| Memorial Sloan-Kettering Cancer Center @ Suffolk | Recruiting |
| Commack, New York, United States, 11725 | |
| Contact: Victoria Blinder, M.D., M.Sc 646-888-4808 | |
| Queens Medical Associates | Not yet recruiting |
| Fresh Meadows, New York, United States, 11366 | |
| Contact: Gabriel Jung, MD | |
| Principal Investigator: Gabriel Jung, MD | |
| Memorial Sloan Kettering Cancer Center | Recruiting |
| New York, New York, United States, 10065 | |
| Contact: Victoria Blinder, M.D., M.Sc 646-888-4808 | |
| Contact: Ethan Basch, M.D., M.Sc 646-422-4426 | |
| Ralph Lauren Center for Cancer Care and Prevention | Recruiting |
| New York, New York, United States | |
| Contact: Joseph R Yoe, MD | |
| Principal Investigator: Joseph R Yoe, MD | |
| Bellevue Hospital Center | Suspended |
| New York, New York, United States | |
| New York Hospital - Queens | Recruiting |
| Queens, New York, United States, 11355 | |
| Contact: Susan H Lee, MD | |
| Principal Investigator: Susan H Lee, MD | |
| Memorial Sloan-Kettering at Mercy Medical Center | Recruiting |
| Rockville Centre, New York, United States | |
| Contact: Victoria Blinder, M.D., M.Sc 646-888-4808 | |
| Memoral Sloan Kettering Cancer Center at Phelps | Recruiting |
| Sleepy Hollow, New York, United States, 10591 | |
| Contact: Victoria Blinder, M.D., M.Sc 646-888-4808 | |
| Principal Investigator: | Victoria Blinder, M.D., M.Sc. | Memorial Sloan-Kettering Cancer Center |
More Information
Additional Information:
No publications provided
| Responsible Party: | Memorial Sloan-Kettering Cancer Center |
| ClinicalTrials.gov Identifier: | NCT01134172 History of Changes |
| Other Study ID Numbers: | 10-071 |
| Study First Received: | May 27, 2010 |
| Last Updated: | January 15, 2013 |
| Health Authority: | United States: Institutional Review Board |
Keywords provided by Memorial Sloan-Kettering Cancer Center:
|
Sociodemographic Ethnicity Work-related Health system |
QOL Questionnaires 10-071 |
Additional relevant MeSH terms:
|
Breast Neoplasms Neoplasms by Site Neoplasms Breast Diseases Skin Diseases |
ClinicalTrials.gov processed this record on June 18, 2013