Smart Phone App Intervention In Young Adults With Cancer
NCT ID: NCT04119869
Last Updated: 2020-12-08
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
25 participants
INTERVENTIONAL
2019-11-11
2020-06-29
Brief Summary
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Detailed Description
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The investigators are conducting this study to see if the iaya app, specifically developed for young adults with cancer, is practical, to determine patient satisfaction with the iaya app, and to test study procedures.
Conditions
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Keywords
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Study Design
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NA
SINGLE_GROUP
SUPPORTIVE_CARE
NONE
Study Groups
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iaya Smart Phone Application
* Pre-study evaluation
* Access to the smartphone intervention over the course of 12 weeks
* Post-study evaluation and interview
iaya
The iaya app is a smartphone application intervention that -through a variety of approaches, such as exercises aimed at identifying and changing thoughts and behaviors, imagery, and relaxation- seeks to enhance coping with the emotional impact of cancer.
Interventions
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iaya
The iaya app is a smartphone application intervention that -through a variety of approaches, such as exercises aimed at identifying and changing thoughts and behaviors, imagery, and relaxation- seeks to enhance coping with the emotional impact of cancer.
Eligibility Criteria
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Inclusion Criteria
* Able to speak/read English
* Have a smart phone
* Receiving cancer treatment
* Active cancer care from an oncologist at Dana-Farber Cancer Institute
Exclusion Criteria
* Adults unable to consent
* Individuals who are not yet adults (infants, children, teenagers)
* Pregnant women
* Prisoners
18 Years
39 Years
ALL
No
Sponsors
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Dana-Farber Cancer Institute
OTHER
Responsible Party
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Hanneke Poort PhD
Principal Investigator
Principal Investigators
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Hanneke Poort, PhD
Role: PRINCIPAL_INVESTIGATOR
Dana-Farber Cancer Institute
Locations
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Dana-Farber Cancer Institute
Boston, Massachusetts, United States
Countries
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Provided Documents
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Document Type: Informed Consent Form
Other Identifiers
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19-333
Identifier Type: -
Identifier Source: org_study_id