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CompletedNCT02833246Updated Nov 19, 2018

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

An interventional study of SMS/MMS text messaging and usual care in Sarcoma, Lung and Solid Tumor Gastrointestinal, sponsored by Memorial Sloan Kettering Cancer Center. Completed at 1 site in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2018-11-19.

Sponsored by Memorial Sloan Kettering Cancer Center · Not applicable, Interventional, and Other

Phase
Not applicable
Study type
Interventional
Enrollment
28
Allocation
Randomized
Ages
18 Years and older
Sex
All
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Study 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.

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Conditions studied

  • Sarcoma
  • Lung
  • Solid Tumor Gastrointestinal

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Keywords

  • texting
  • Adherence to Oral Anticancer Medications
  • 16-810
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In context

Sarcoma

1,667 studies on the registry are indexed under Sarcoma; 393 are open to participants now.

This study's enrollment of 28 is below the median of 40 across 1,283 interventional studies indexed under Sarcoma.

Browse Sarcoma studies →

Lead sponsor

Memorial Sloan Kettering Cancer Center is the lead sponsor of 1,930 studies on the registry; 328 are open to participants now.

Of its 129 completed or terminated interventional studies of FDA-regulated products, 66 (51%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

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

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.
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Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
28 participants (actual)

Study arms

  • Experimental
    SMS/MMS text messaging

    Patients will be able to tailor their SMS/MMS reminders with respect to when (i.e., what time of day) they wish to receive the reminders, as well as how often the messages are sent (e.g., morning and evening).

    Other: SMS/MMS text messaging

  • Active comparator
    usual care

    This includes physician and nursing assessment and intervention for any identified AEs. Of note, there is not currently standard follow-up that patients receive from nursing or physician staff while on an OAM treatment. Patients are encouraged to call their physician's office with any questions or changes in their medical status but are not called routinely by MSK staff.

    Other: usual care

Interventions

  • OtherSMS/MMS text messaging

    text messaging reminders on oral chemotherapy medication adherence

  • Otherusual care
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What researchers measure

Primary outcomes

  1. objective pill count

    is greater or less than the amount of OAM that the patient should have in their possession.

    Time frame: 1 year

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Study locations

1 site
  • Memorial Sloan Kettering Cancer Center
    New York, New York 10065, United States
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References and documents

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Nov 19, 2018, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT02833246
Lead sponsor
Memorial Sloan Kettering Cancer Center
Responsible party
Sponsor
First posted
Jul 14, 2016
Start date
Jun 28, 2016
Primary completion
Nov 14, 2018
Completion
Nov 14, 2018
Last update
Nov 19, 2018

Study contacts

Thomas Atkinson, PhD
principal investigator · Memorial Sloan Kettering Cancer Center
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Nov 2018. You cannot join it, but the record below documents what was studied.

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