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

This trial's timeline: 3 weeks for screening, Varies for treatment, and up to 5 years for reporting.

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.

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