- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03697083
Reminders Through Association & Prescription Adherence
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Participants enter an online survey where they are asked to confirm that they plan to pick up a prescription, state what day they plan to pick up their prescription, and indicate the type of location where the prescription will be picked up (e.g., pharmacy, hospital, doctors office, etc.). Participants are asked to participate in a prescription reminder program in which they will receive up to eight text messages from the researchers and send up to three text messages to the researchers. Participants are then quizzed about the reminder program to ensure they understand what they are signing up for. Participants are further told that if they follow the directions outlined in the program they will be compensated for participating in this survey via their phone number.
Participants who wish to enroll in the reminder program will initiate the text messaging by texting "STARTXXXX" to number provided. This validates that the participants received the message, have the capacity to text, and are willing to text. Participants are then randomly assigned to one of three conditions. In the treatment condition, participants will be prompted to think of a reminder cue that will help them remember to pick up the prescription. In the active control condition, participants will be asked to think about where they will store their prescription. Participants in the baseline control condition will simply be thanked for enrolling.
Participants in the treatment and active control conditions then receive a series of text messages prior to the scheduled pick up date reminding them to pick up their medication. In addition, the text message will prompt participants to text a picture of their prescription receipt to validate that they followed-through on their behavior. If participants text us a picture of their receipt that follows the guidelines outlined in the survey, participants are compensated.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Pennsylvania
-
Philadelphia, Pennsylvania, United States, 19104
- University of Pennsylvania
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Participants must be capable of sending and receiving text and picture messages on their phone.
Exclusion Criteria:
- Participants will only be excluded if they participated in the pilot study in which the investigators enrolled 150 participants. These participants will be excluded when they attempt to text the investigators to enroll.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: HEALTH_SERVICES_RESEARCH
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: NONE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
EXPERIMENTAL: Reminders Through Association Arm
participants will be prompted to think of a reminder cue that will help them remember to pick up the prescription.
|
Participants receive 8 text messages asking them to think of a reminder cue that will help them remember to pick up the prescription and use the cue.
|
|
ACTIVE_COMPARATOR: Active Control Arm
Participants will be asked to think about where they will store their prescription.
|
Participants receive 8 text messages asking them to think of where they plan to store their medication once they pick it up and to think about that location on their intended date of pickup.
|
|
ACTIVE_COMPARATOR: Baseline Control Arm
Participants are thanked for enrolling in the reminder program.
|
Participants receive 1 text message thanking participants for enrolling in the reminder program.
Participants are not contacted further.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Picking up Prescription on Intended Date of Pickup
Time Frame: The time frame can range from less than 1 day to a maximum of 7 days.
|
At the beginning of the study, participants indicate the date they plan to pick up their prescription. Participants are later asked to text a picture of their prescription receipt to the experimenter after they complete the prescription reminder program. The receipt must satisfy three criteria:
the investigators' primary dependent variable is binary taking the value one if the participant sends a picture of their receipt to the investigators that satisfies all criteria stated above and taking the value zero if otherwise. |
The time frame can range from less than 1 day to a maximum of 7 days.
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (ACTUAL)
Primary Completion (ACTUAL)
Study Completion (ACTUAL)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ACTUAL)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 825556
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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