Your session is about to expire
← Back to Search
Behavioural Intervention
Online Program for Medication Adherence
N/A
Waitlist Available
Led By Steve R Feldman, MD, PhD
Research Sponsored by Wake Forest University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 5 years
Awards & highlights
No Placebo-Only Group
Summary
This trial will test whether an online program can help improve medication adherence.
Who is the study for?
This trial is for adults over 18 who are currently taking oral medications for high blood pressure, high cholesterol, diabetes, or depression and get their prescriptions from specific pharmacies. Participants must plan to use the same pharmacy for the next year and be able to complete surveys online in English.
What is being tested?
The study is testing an Internet-based intervention designed to improve medication usage among patients with certain chronic conditions. It involves participants completing internet surveys about their experience with medications.
What are the potential side effects?
Since this trial involves completing internet surveys rather than testing a new medication or medical device, there are no direct physical side effects associated with participating in this research.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ up to 5 years
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 5 years
Treatment Details
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
4Treatment groups
Experimental Treatment
Active Control
Group I: Intervention Group CExperimental Treatment1 Intervention
Randomization occurs after enrollment survey has been completed. This group will complete weekly internet surveys for eight weeks. Upon secondary randomization at week eight, the group will not receive any more internet surveys. They will be asked to complete the final survey.
Group II: Intervention Group BExperimental Treatment1 Intervention
Randomization occurs after enrollment survey has been completed. This group will complete weekly internet surveys for eight weeks. Upon secondary randomization at week eight, this group will begin to receive monthly internet surveys. They will be asked to complete the final survey.
Group III: Intervention Group AExperimental Treatment1 Intervention
Randomization occurs after enrollment survey has been completed. Upon secondary randomization at week eight, this group will continue to receive weekly internet surveys for the entire twelve months. They will be asked to complete the final survey.
Group IV: ControlActive Control1 Intervention
Randomization occurs after enrollment survey has been completed. This group will not receive the internet intervention for the twelve months. They will be asked to complete the final survey.
Find a Location
Who is running the clinical trial?
Wake Forest UniversityLead Sponsor
192 Previous Clinical Trials
166,050 Total Patients Enrolled
Steve R Feldman, MD, PhDPrincipal InvestigatorWake Forest University Health Sciences
2 Previous Clinical Trials
424 Total Patients Enrolled