A Theoretically Informed mHealth Intervention to Improve Medication Adherence by Adults with Chronic Conditions: Technology Acceptance Model-Based Smartphone Medication Reminder App Training Session

  • STATUS
    Recruiting
Updated on 19 February 2024

Summary

As a potential way to support your medication taking and management, the aim of this study is to promote your smartphone medication reminder app use. To meet this aim, the purpose of this study is to provide you with a group session introducing a smartphone medication reminder app and to assess whether the group session is helpful for promoting app use.

Description

You will be asked to take part in a 2-hour group session.  You will learn about one smartphone medication reminder app.  In addition you will be asked what you think about the app and the group session.  We will conduct the study at a private room at IUPUI or another more conveniently located community site. 

Participants will be compensated for their participation.

Details
Condition Chronic condition
Age 40years - 100years
Clinical Study IdentifierTX10231
Last Modified on19 February 2024

Eligibility

How to participate?

Step 1 Connect with a study center
Message sent successfully.
We have submitted the information you provided to the research team at the location you chose. For your records, we have sent a copy of the message to your email address.
If you would like to be informed of other studies that may be of interest to you, you may sign up for Patient Notification Service.
Sign up

Send a message

Enter your contact details to connect with study team


Email

View email

Phone

Phone country flag

View phone
Investigator Avatar

Primary Contact

First name*
Last name*
Email*
Phone number*
Preferred way of contact label
Race
Ethnicity
Other language

Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

Learn more

If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

Learn more

Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

Learn more

Similar trials to consider

Loading...

Not finding what you're looking for?

Every year hundreds of thousands of volunteers step forward to participate in research. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.

Sign up as volunteer
Add a private note
  • abc Select a piece of text.
  • Add notes visible only to you.
  • Send it to people through a passcode protected link.