- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02411006
Effect of Reminders on Adherence
September 26, 2016 updated by: University of Pennsylvania
Prediction and Pre-commitment Mailings for Medication Adherence
The investigators seek to increase medication adherence of subjects.
The investigators will send mailings to customers of an insurance company, asking them to predict or commit to a certain level of behavior.
The investigators will measure whether this increases medication adherence.
Study Overview
Status
Completed
Conditions
Detailed Description
The investigators seek to increase medication adherence of subjects.
The investigators will send mailings to customers of an insurance company, asking them to predict or commit to a certain level of behavior.
The investigators will measure whether this increases medication adherence.
The investigators will send mailings to subjects once per month, and elicit responses via mail, phone, and web surveys.
Study Type
Interventional
Enrollment (Actual)
47088
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
-
-
Pennsylvania
-
Philadelphia, Pennsylvania, United States, 19104
- University of Pennsylvania
-
-
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
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- customers of the investigators' insurance company partner
Exclusion Criteria:
- none
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: Prevention
- Allocation: Randomized
- Interventional Model: Factorial Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
No Intervention: Usual care control
No intervention, just usual care from the insurance company
|
|
Experimental: Reminder control
Send a reminder to subjects every month
|
Remind people to take their medicine
|
Experimental: Anonymous prediction
Ask subjects to anonymously predict their upcoming medication adherence
|
Remind people to take their medicine
Ask people to predict their upcoming medication adherence
Keep patient predictions and commitment anonymous
|
Experimental: Anonymous commitment
Ask subjects to anonymously commit to their upcoming medication adherence
|
Remind people to take their medicine
Keep patient predictions and commitment anonymous
Ask people to commit to their upcoming medication adherence
|
Experimental: Identified prediction
Ask subjects to predict their upcoming medication adherence and report it
|
Remind people to take their medicine
Ask people to predict their upcoming medication adherence
Ask patients to report their predictions and commitments
|
Experimental: Identified commitment
Ask subjects to commit to their upcoming medication adherence and report it
|
Remind people to take their medicine
Ask people to commit to their upcoming medication adherence
Ask patients to report their predictions and commitments
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Medication refills
Time Frame: 6 months
|
frequency of refilling medication
|
6 months
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Hemoglobin A1C
Time Frame: 6 months
|
6 months
|
LDL cholesterol
Time Frame: 6 months
|
6 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Katherine Milkman, Ph.D, University of Pennsylvania
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
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
November 1, 2014
Primary Completion (Actual)
June 1, 2015
Study Completion (Actual)
June 1, 2015
Study Registration Dates
First Submitted
April 3, 2015
First Submitted That Met QC Criteria
April 7, 2015
First Posted (Estimate)
April 8, 2015
Study Record Updates
Last Update Posted (Estimate)
September 27, 2016
Last Update Submitted That Met QC Criteria
September 26, 2016
Last Verified
September 1, 2016
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- H14P001
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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