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Mobile App Based Personalized Solutions and Tools for Medication Adherence of Rx Pills

NCT02072005 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 11

Last updated 2014-07-31

No results posted yet for this study

Summary

The primary aim of this study is to conduct a 9-patient feasibility and acceptability study of mSMART (with future studies focusing on improved medication adherence). The sample will include daily smokers who are already taking a prescribed medication. There will be no change in any medication regimen in this study, and the sample will include smokers either with or without a psychiatric disorder. Subjects will be asked to use a smartphone application, or "app" (i.e. mSMART) that will provide information about their medication and when to take it. Along with smart phone, the participants will be asked to utilize an electronic pillbox (i.e. GlowCap) to further assist with medication compliance.

Conditions

  • Cigarette Smoking

Interventions

OTHER

mSMART smartphone application

This application is an interface that provides subjects with information and questionnaires related to their medication.

Sponsors & Collaborators

  • Intelligent Automation, Inc.

    collaborator INDUSTRY

  • National Institute on Drug Abuse (NIDA)

    collaborator NIH

  • Duke University

    lead OTHER

Principal Investigators

  • John T Mitchell, Ph.D. · Duke University

Eligibility

Min Age
18 Years
Max Age
50 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-02-28
Primary Completion
2014-04-30
Completion
2014-04-30

Countries

  • United States

Study Locations

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Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02072005 on ClinicalTrials.gov