Improving Informed Decision Making for Cancer Clinical Trial Participation
Lay Description
The goal of this study is to develop and pilot test a multi-communication approach to improve informed decision-making about cancer Clinical Trials (CTs) participation by increasing awareness of CTs and Mays Cancer Center (MCC) services (treatment care capacities, reputation and resources), positive attitudes towards CTs, self-efficacy and intentions to consider CTs as an appropriate treatment option for cancer (intention to participate) among patients attending the MCC (clinic-based setting) and the general public in selected Bexar County areas (community-based settings).
Category
- Cancers and Other Neoplasms
- IRB Number
- 20180283HU
- NCT Number
- NCT03820687
Eligibility
- Eligible Ages
- Over 18 Years
- Eligible Genders
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- Newly diagnosed cancer patients attending any of the clinics at the MCC
- Patients who have not had a consultation with their doctor to discuss treatment options
- Patients who have not participated in a Clinical Trial before
- English or Spanish speaking
- Able to provide informed consent
Exclusion Criteria
- Younger than 18 years
- Patients who have already had a consultation with their doctor to discuss treatment options
- Patients who have participated in a Clinical Trial before
- Unable to provide informed consent
Study Design
Arm Groups
Study Contact
Patricia Chalela
210-562-6513
chalela@uthscsa.edu
Principal Investigator
Amelie Ramirez