Follow-up Care Among Vulnerable Cancer Survivors
D
David Haggstrom, MD
Primary Investigator
J
Jessica MacLean
Primary Investigator
Administratively Closed
100 years or below
All
Phase
N/A
2 Locations
Brief description of study
What is the purpose of this study?
A longitudinal cohort study will be performed among cancer survivors diagnosed in the state of Indiana from 2001-2010 in order to determine whether there are differences in the quality of surveillance care processes among socially vulnerable populations.
THIS STUDY IS ENROLLING BY INVITATION ONLY - Consistent with most oncology trials, patients are not actively “recruited,” but are screened by their physician for appropriate clinical trial(s) at the time of their routine clinic visit. Occasionally, a patient may be a self-referral or physician referral, but are still screened for appropriate clinical trials at the time of their routine clinic visit. PI and staff may send copies of relevant consent forms to these patients to look over prior to actually consenting or enrolling them. This may take place at the patient's visit at which the consent is presented or the patient's next visit to the outpatient hematology/oncology clinic.
Interested in participating? For more information about this research study or other cancer-related clinical trials at IU Simon Comprehensive Cancer Center, please contact:
IU Clinical Trials Office
Email: iutrials@iu.edu
Phone: (317) 278-5632
Eligibility of study
You may be eligible for this study if you meet the following criteria:
- Conditions: Cancer
-
Age: 100 years or below
-
Gender: All
Updated on
13 Nov 2024.
Study ID: IUCRO-0457, 1311856317
