Aging and Cancer Effects (ACE) Study

This study has been completed.
Information provided by (Responsible Party):
University of Wisconsin, Madison Identifier:
First received: September 13, 2005
Last updated: October 1, 2015
Last verified: September 2010


  1. Subjective self-reported data can be used to accurately reflect functioning across the 5 key domains.
  2. Cancer and its various treatment modalities will exert detrimental effects on the 5 key domains in older adults with cancer.
  3. Some aspect of baseline patient characteristic will be predictive of cancer-related outcomes.

Breast Cancer
Lung Cancer

Study Type: Observational
Study Design: Observational Model: Case-Only
Time Perspective: Prospective
Official Title: Aging and Cancer: The Effects of Comorbidities on Cancer and it's Treatment

Resource links provided by NLM:

Further study details as provided by University of Wisconsin, Madison:

Enrollment: 34
Study Start Date: February 2005
Study Completion Date: December 2009
Primary Completion Date: December 2009 (Final data collection date for primary outcome measure)

Ages Eligible for Study:   55 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
Men and women over the age of 55 newly diagnosed with lung, breast, colon or rectal cancer, and with an anticipated life expectancy of at least 2 years for breast cancer patients,1 year for patients with lung cancer, and 2 years for patients with colon or rectal cancer. There is no upper age limit for participation in this study.

Inclusion Criteria:

  • Willing to do memory testing
  • Willing to participate in activities of daily living assessment
  • Can use a cane or walker
  • Willing to complete a balance performance assessment, if able.

Exclusion Criteria:

  • Currently receiving treatment for cancer.
  • Has a previous history of brain cancer
  • Significant neurological disease other than AD that might affect cognitive function, such as stroke, Parkinson's disease, multiple sclerosis, or serious traumatic brain injury.
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its identifier: NCT00204880

United States, Wisconsin
University of Wisconsin
Madison, Wisconsin, United States, 53792
Sponsors and Collaborators
University of Wisconsin, Madison
Principal Investigator: Sanjay Asthana, MD University of Wisconsin, Madison
  More Information

No publications provided

Responsible Party: University of Wisconsin, Madison Identifier: NCT00204880     History of Changes
Other Study ID Numbers: 2004-0341
Study First Received: September 13, 2005
Last Updated: October 1, 2015
Health Authority: United States: Institutional Review Board processed this record on November 27, 2015