- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03810053
Utilizing Technology to Promote Cancer Prevention
September 28, 2021 updated by: University of Arkansas
The goal of the program is to develop an online module/a health application for cell phones which will share didactic information regarding cancer prevention and early detection measures.
These module/application will be developed, and be tested among volunteers for feedback.
In the future, these module/application will be disseminated widely to address cancer health disparity particularly in Arkansas.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
The application or the online module will play a short didactic explanation video that will provide information about cancers and benefits of uptake of cancer prevention and early detection measures.
It is currently unknown which method will be used, the online module or the application for the purpose.
The study participants will be subjected to only one method (once the method have been finalized and created).
The video content will engulf information about cervical, breast, colorectal and lung cancer prevention and early detection.
After the video, the application or the module will capture information on gender, age, smoking status, body mass index and positive cancer history in family.
Watching the video and answering the questions will take approximately 5 minutes.
The study participants will download the application on their personal cell phones and the data collected will be linked to identifying information in case they choose to receive the compensation and opt for the 6-month follow-up.
Based on the responses provided, and the age and the gender, the participants will be provided with a list of cancer prevention and early detection measure(s).
A subset of the study participants from ARResearch (only those who have agreed for the 6-month follow-up) will be asked if they are willing to be contacted by the study staff after 6 ±1 months (from the date of enrollment in the study) to enquire if they received/adopted the screening measures(s) that were suggested based on their age, gender and family history.
They will be asked whether it is OK to call and/or e-mail them for more information to better describe barriers to obtaining cancer prevention and screening measures.
Study Type
Interventional
Enrollment (Actual)
290
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Arkansas
-
Little Rock, Arkansas, United States, 72205
- University of Arkansas for Medical Sciences
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
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.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
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.
|
Short didactic explainer video that will provide information about cancers and benefits of uptake of cancer prevention and early detection measures.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Percentage of Participants to Learn New Information
Time Frame: up to 6 Months
|
Percentage of participants that indicated they learned something new about cancer prevention measures.
|
up to 6 Months
|
|
Percentage of Participants to Identify Needed Interventions
Time Frame: up to 6 months
|
Percentage of participants that identified interventions that they have not yet adopted from the use of the health application.
|
up to 6 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Mayumi Nakagawa, Ph.D, University of Arkansas
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
March 1, 2019
Primary Completion (Actual)
December 20, 2019
Study Completion (Actual)
July 14, 2021
Study Registration Dates
First Submitted
January 9, 2019
First Submitted That Met QC Criteria
January 17, 2019
First Posted (Actual)
January 18, 2019
Study Record Updates
Last Update Posted (Actual)
October 20, 2021
Last Update Submitted That Met QC Criteria
September 28, 2021
Last Verified
July 1, 2021
More Information
Terms related to this study
Other Study ID Numbers
- 228815
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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