Overview

This trial is active, not recruiting.

Condition breast cancer
Treatment questionnaires
Sponsor Memorial Sloan Kettering Cancer Center
Collaborator University of Texas Southwestern Medical Center
Start date October 2001
End date December 2017
Trial size 650 participants
Trial identifier NCT00582478, 01-120

Summary

The purpose of this study is to look at how breast cancer treatment affects quality of life in women of different ages. The U.S. Army Breast Cancer Research Program funds this study. In this research project, we wish to study a woman's quality of life after breast cancer treatment as related to her health. We want to know how you feel about your quality of life.

United States No locations recruiting
Other Countries No locations recruiting

Study Design

Observational model case-only
Time perspective prospective
Arm
women with breast cancer
questionnaires Functional Assessment of Cancer Therapy - Fact B, 2. Beck Depression Inventory, 3. MOS Sexual Functioning
Participants will be followed regularly at 3, 6, 12, and 18-month intervals

Primary Outcomes

Measure
The study measurements are quality of life questionnaires
time frame: 7 years 2 months

Eligibility Criteria

Female participants at least 18 years old.

Inclusion Criteria: - Female - Aged 18 or older at the time of breast cancer diagnosis - English-speaking - Community dwelling (i.e. not living in a residential care or correctional facility) - Diagnosed with invasive breast cancer Stage I, II, or III within the previous 6 months - First time diagnosis - Have physician agreement for participation - Provide informed consent Exclusion Criteria: - Psychiatric or psychological abnormality precluding informed consent or ability to complete questionnaires - Previous or concurrent malignancy (except basal and squamous skin cancer and stage 0 cervical cancer) - Stage IV breast malignancy - Residency outside of the United States - For women ages 45 years and younger only: Those participants < 45 years who were having regular menstrual cycles at the time of diagnosis will be excluded from this protocol. This study will only be enrolling women in this age category who have had a prior hysterectomy or were having irregular menstrual cycles at the time of diagnosis. Women with regular menstrual cycles will be enrolled into a companion project (i.e., Menstrual Cycle Maintenance

Additional Information

Official title Investigating Mechanisms to Explain Age Associated Differences in Quality of Life Among Breast Cancer Patients
Principal investigator Kimberly Van Zee, MD
Description This multi-center study will include self-referred. This project is a prospective cohort study of 800 women aged 18 and over who are newly diagnosed with breast cancer. Women will be recruited into the study within 6 months after diagnosis and followed for 18 months. The primary purpose of the proposed study is to examine mechanisms that may explain age differences in the health-related quality of life of women who have been diagnosed with a first-time breast cancer. The studies will examine psychosocial factors such as social support, coping strategies, resiliency, and the impact of cancer on life responsibilities as explanations of age-associated factors affecting HRQL. This project is an observational, longitudinal study of women aged 18 and over who are newly diagnosed with breast cancer. In order to examine both the short- and longer-term impact of breast cancer on HRQL, the study will survey women post diagnosis and follow them at 3, 6, 12, and 18 months. A secondary purpose is to have this large cohort of breast cancer patients serve as a comparison group for other studies in the Behavioral Center of Excellence award given to Wake Forest Medical Center by the Department of Defense. Extensive baseline data will be collected by an in-depth chart review and interview for additional data. Information will be gathered on demographics, clinical and treatment variables. The study intervention consists of collecting data on health-related quality of life through specific questionnaires. Data collection instruments will be mailed to participants at regularly scheduled intervals accompanied by a stamped,addressed envelope. If the participant does not return study forms within three weeks, the participant will be called.
Trial information was received from ClinicalTrials.gov and was last updated in November 2016.
Information provided to ClinicalTrials.gov by Memorial Sloan Kettering Cancer Center.