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Effect of Multi-Media Enrollment

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ClinicalTrials.gov Identifier: NCT02020252
Recruitment Status : Unknown
Verified January 2018 by University of Chicago.
Recruitment status was:  Active, not recruiting
First Posted : December 24, 2013
Last Update Posted : January 4, 2018
Sponsor:
Information provided by (Responsible Party):
University of Chicago

Study Description
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Brief Summary:
The purpose of this research study is to test a touchscreen computer program, which allows patients to see information on a computer screen regarding cancer care, and specifically clinical trials. The purpose of this research is to help the investigators learn more about how to use technology in the medical setting to improve health outcomes.

Condition or disease Intervention/treatment
Lung Cancer Other: Touchscreen Computer Program

Study Design
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Study Type : Observational
Actual Enrollment : 120 participants
Observational Model: Other
Time Perspective: Prospective
Official Title: A Pilot Investigation to Examine the Effect of a Multi-Media, Computer Based Tool (Talking Touchscreen) on Enrollment in Adult Oncology-Specific Clinical Trials at an Academic Medical Center
Actual Study Start Date : November 26, 2013
Estimated Primary Completion Date : October 2018
Estimated Study Completion Date : November 2018

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Groups and Cohorts
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Group/Cohort Intervention/treatment
Touchscreen Participants Other: Touchscreen Computer Program
A program which allows patients to see information on a computer screen regarding cancer care, and specifically clinical trials


Outcome Measures
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Primary Outcome Measures :
  1. Change in attitudes, knowledge, and clinical trial decision making after use of interactive multimedia learning program [ Time Frame: 1 day ]
    To determine whether talking touchscreen (TT) delivery of educational clinical trial information can improve clinical trial knowledge overall and within low literacy populations, in particular.


Eligibility Criteria
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Information from the National Library of Medicine

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, Learn About Clinical Studies.


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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
Patients at the University of Chicago Medical Center
Criteria

Inclusion Criteria:

  • New patients presenting at the University of Chicago outpatient oncology clinics.
Contacts and Locations
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Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02020252


Locations
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United States, Illinois
University of Chicago Comprehensive Cancer Center
Chicago, Illinois, United States, 60637
Sponsors and Collaborators
University of Chicago
Investigators
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Principal Investigator: Blase Polite, MD University of Chicago Comprehensive Cancer Center
More Information
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Responsible Party: University of Chicago
ClinicalTrials.gov Identifier: NCT02020252    
Other Study ID Numbers: IRB13-1233
First Posted: December 24, 2013    Key Record Dates
Last Update Posted: January 4, 2018
Last Verified: January 2018