- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01696331
Text Messaging for Adherence in Adolescent Liver Transplant Recipients
April 17, 2018 updated by: Rebecca Berquist McKenzie, Stanford University
Impact of Text Messaging on Adherence in Adolescent Liver Transplant Patients
Text message reminders will improve adherence to lab tests in adolescent liver transplant recipients.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Adolescent patients who received a liver transplant will be recruited to participate in receiving text message reminders for lab tests.
They will be send de-identified messages according to their required lab schedule.
The investigators will monitor their adherence to lab tests as well as medication and clinic visits.
They will also have a questionnaire about their medical regimen before and at the end of the study.
Study Type
Interventional
Enrollment (Actual)
42
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
California
-
Palo Alto, California, United States, 94304
- Lucile Packard Children's Hospital
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
12 years to 25 years (ADULT, CHILD)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Patient >12 years
- Received liver transplant
- Followed by Stanford Liver Transplant Team
Exclusion Criteria:
- No personal cell phone
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: HEALTH_SERVICES_RESEARCH
- Allocation: NA
- Interventional Model: SINGLE_GROUP
- Masking: NONE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
EXPERIMENTAL: Text Message Reminder
|
Sent TM reminder at beginning and end of each month that corresponded to required lab frequency.
Patients were able to send autoresponses.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Adherence to lab tests
Time Frame: One year
|
One year
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Texting responses
Time Frame: 1 year
|
Correspondence between actual completion of tests versus reported
|
1 year
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
September 1, 2012
Primary Completion (ACTUAL)
January 1, 2013
Study Completion (ACTUAL)
January 1, 2013
Study Registration Dates
First Submitted
September 27, 2012
First Submitted That Met QC Criteria
September 28, 2012
First Posted (ESTIMATE)
October 1, 2012
Study Record Updates
Last Update Posted (ACTUAL)
April 19, 2018
Last Update Submitted That Met QC Criteria
April 17, 2018
Last Verified
April 1, 2018
More Information
Terms related to this study
Other Study ID Numbers
- 25318
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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