Smart-phone Application to Promote Medication Adherence in Adolescents and Young Adults (AYA) With Cancer
This trial has been completed.
|Sponsor||University of Utah|
|Collaborator||Oncology Nursing Society Foundation|
|Start date||May 2012|
|End date||December 2016|
|Trial size||32 participants|
|Trial identifier||NCT01618344, SCH-13929|
To explore use of a smart-phone medication reminder application to promote adherence to oral medications by AYA with cancer.
Feasibility and acceptability of using a smart-phone medication reminder application to promote adherence to oral medications by AYA with cancer.
time frame: ongoing study weeks 5-12
All participants from 15 years up to 29 years old.
Inclusion criteria: 1)15-29 year olds receiving treatment for any type of cancer, either primary or recurrent/relapsed disease. 2) Patient has completed at least one month of therapy 3)Patient is expected to remain on therapy for 3 month duration of study 4) Patient has an iPhone, iPad, or iTouch running iOS 4.0 or later 5) Patient is willing to use a smart-phone medication reminder application- Exclusion Criteria: 1)Patients who are unable to speak/read/write English as required for use of smart-phone medication reminder application and completion of study measures.
|Official title||Use of a Smart-phone Medication Reminder Application to Promote Adherence to Oral Medications by Adolescents and Young Adults(AYA) With Cancer|
|Principal investigator||Yelena Wu, MD|
|Description||Non-adherence to oral medications is a prevalent problem in adolescents and young adults (AYA) with cancer that may impact both survival and quality of life while on treatment. The purpose of this study is to explore use of a smart-phone medication reminder application to promote adherence to oral medications by AYA with cancer. The study's primary aim is to explore the feasibility and acceptability of using a smart-phone medication reminder application to promote adherence to oral medications by AYA with cancer as well as to characterize application use. Secondary aims include: 1) to obtain initial estimates of intervention effect- measured by pre-intervention to post-intervention differences in perceived behavioral control for adherence, intention to adhere, and adherence behavior - to inform design of a future trial powered to detect a clinically significant effect of smart-phone medication reminder application use on adherence to oral medications; and 2) to examine the relationships among perceived behavioral control for adherence, intention to adhere, and adherence behavior. A pre-post single group design will be used. Data will be collected weekly for 4 weeks before introduction of the intervention and for 8 weeks following introduction of the intervention. Analytic approaches will include descriptive statistics and generalized estimating equation (GEE) modeling.|
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