Utilizing Technology to Promote Cancer Prevention
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The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details. |
ClinicalTrials.gov Identifier: NCT03810053 |
Recruitment Status :
Not yet recruiting
First Posted : January 18, 2019
Last Update Posted : February 5, 2019
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Condition or disease | Intervention/treatment | Phase |
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Health Knowledge, Attitudes, Practice | Behavioral: Mobile App/Online Module | Not Applicable |
Study Type : | Interventional (Clinical Trial) |
Estimated Enrollment : | 300 participants |
Intervention Model: | Single Group Assignment |
Masking: | None (Open Label) |
Primary Purpose: | Health Services Research |
Official Title: | Utilizing Technology to Promote Cancer Prevention |
Estimated Study Start Date : | April 2019 |
Estimated Primary Completion Date : | January 2020 |
Estimated Study Completion Date : | March 2020 |
Arm | Intervention/treatment |
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Experimental: Mobile App/Online Module
Subjects will watch a short video containing information about cancers and benefits of uptake cancer prevention and early detection measures. Information regarding gender, age, smoking status, BMI and positive cancer history in family will be captured. Subjects will be provided with a list of cancer prevention and early detection measures based on the responses provided.
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Behavioral: Mobile App/Online Module
Short didactic explainer video that will provide information about cancers and benefits of uptake of cancer prevention and early detection measures. |
- The Effectiveness of an Online Module in Teaching New Information [ Time Frame: up to 6 Months ]This study will address the number of participants who have learned something new from the development of a health application for cell phones or an online module.
- The Effectiveness of an Online Module in Identifying Needed Interventions [ Time Frame: up to 6 months ]The study will also address the number of participants that identified interventions that they have not yet adopted from the use of the health application.

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Ages Eligible for Study: | 18 Years and older (Adult, Older Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
- Any ARResearch volunteer.
- 18 years or older in age.
- Have access to a personal cell phone and/or computer
Exclusion Criteria:
- Unable to give an informed consent.

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): NCT03810053
Contact: Maumi Nakagawa, MD, PhD | 501-686-8635 | MNakagawa@uams.edu | |
Contact: Beth Scanlan | 501-686-8274 | bscanlan@uams.edu |
Principal Investigator: | Maumi Nakagawa, Ph.D | University of Arkansas |
Responsible Party: | University of Arkansas |
ClinicalTrials.gov Identifier: | NCT03810053 History of Changes |
Other Study ID Numbers: |
228815 |
First Posted: | January 18, 2019 Key Record Dates |
Last Update Posted: | February 5, 2019 |
Last Verified: | February 2019 |
Studies a U.S. FDA-regulated Drug Product: | No | |
Studies a U.S. FDA-regulated Device Product: | No |