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Quality of Life in Female Breast Cancer Survivors and Their Spouse, Partner, or Acquaintance

NCT00309933 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 2697

Last updated 2023-06-18

No results posted yet for this study

Summary

RATIONALE: Studying quality of life in breast cancer survivors may help determine the long-term effects of breast cancer and may help improve the quality of life for future breast cancer survivors.

PURPOSE: This clinical trial is studying quality of life in female breast cancer survivors and their spouse, partner, or acquaintance.

Conditions

  • Breast Cancer
  • Cancer Survivor
  • Cognitive/Functional Effects
  • Psychosocial Effects of Cancer and Its Treatment
  • Sexuality and Reproductive Issues
  • Spiritual Concerns

Interventions

PROCEDURE

cognitive assessment

PROCEDURE

psychosocial assessment and care

PROCEDURE

quality-of-life assessment

Sponsors & Collaborators

  • National Cancer Institute (NCI)

    collaborator NIH

  • Eastern Cooperative Oncology Group

    lead NETWORK

Principal Investigators

  • Victoria Champion, DNS · Indiana University Melvin and Bren Simon Cancer Center

  • George W. Sledge, MD · Indiana University Melvin and Bren Simon Cancer Center

  • Lynne Wagner, MD · Robert H. Lurie Cancer Center

Eligibility

Min Age
18 Years
Max Age
78 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2006-04-03
Primary Completion
2011-03-31
Completion
2011-03-31

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00309933 on ClinicalTrials.gov