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NCT02833246 Clinical Trial

Using a Patient-Centered mHealth Intervention to Improve Adherence to Oral Anticancer Medications

Sarcoma Clinical Trial

Official title:
Using a Patient-Centered mHealth Intervention to Improve Adherence to Oral Anticancer Medications

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT02833246
Other study ID # 16-810
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date June 28, 2016
Est. completion date November 14, 2018

Study information
Verified date November 2018
Source Memorial Sloan Kettering Cancer Center
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study is being done to determine if sending reminder text messages helps patients take their Oral Anticancer Medication (OAMs) when they are supposed to.

Recruitment information / eligibility
Status Completed
Enrollment 28
Est. completion date November 14, 2018
Est. primary completion date November 14, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Patient in the Sarcoma, Solid Tumor Gastrointestinal (ST GI), and Thoracic Medicine service at MSK.

- Starting a new treatment regimen that includes a single oral anticancer medication

- Patients must have a mobile phone that can send and receive SMS/MMS messages and is internet-enabled.

- Age 18 or older.

- Ability to speak and read English because we do not have the resources to translate the text messages into other languages.

Exclusion Criteria:

- Patient expresses inability or unfamiliarity with using SMS/MMS messaging on their phone and is unwilling to be trained in the use of this technology.

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• SMS/MMS text messaging
text messaging reminders on oral chemotherapy medication adherence
• usual care

Locations
Country Name City State
United States Memorial Sloan Kettering Cancer Center New York New York

Sponsors (1)
Lead Sponsor Collaborator
Memorial Sloan Kettering Cancer Center

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary objective pill count is greater or less than the amount of OAM that the patient should have in their possession. 1 year
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