Completed

Using an Internet Survey to Improve Patient Adherence in Chronic Disease

0 criteria met from your profileSee at a glance how your profile meets each eligibility criteria.
What is being tested

Internet Survey

+ Internet Survey

+ Internet Survey

Other
Who is being recruted

Behavior+12

+ Behavioral Symptoms

+ Cardiovascular Diseases

Over 18 Years
+3 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Other Study

Interventional
Study Start: October 2012
See protocol details

Summary

Principal SponsorWake Forest University
Last updated: July 3, 2025
Sourced from a government-validated database.Claim as a partner

Study start date: October 1, 2012

Actual date on which the first participant was enrolled.

The purpose of this study is to evaluate whether participation in an Internet-based intervention helps improve medication use.

Principal SponsorWake Forest University
Last updated: July 3, 2025
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

186 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Other Study

Some studies explore topics that don't fall into a specific category. These might include innovative research, new technologies, or emerging healthcare areas.



Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

Over 18 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

BehaviorBehavioral SymptomsCardiovascular DiseasesEndocrine System DiseasesHyperlipidemiasMetabolic DiseasesNutritional and Metabolic DiseasesVascular DiseasesGlucose Metabolism DisordersDyslipidemiasLipid Metabolism DisordersDepressionDiabetes MellitusHypercholesterolemiaHypertension

Criteria

1 inclusion criteria required to participate
Any male or female 18 years or older, filling prescriptions for oral medications for hypertension, high cholesterol, diabetes, or depression at the Downtown Health Plaza, Piedmont Plaza, or Cancer Center Pharmacies

2 exclusion criteria prevent from participating
Inability to complete Internet surveys due to inadequate Internet access, not understanding a survey written in English, or lack of computer skills

Patient does not intend to continue using the same WFBMC-affiliated pharmacy for the next 12 months

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

4 intervention groups are designated in this study

This study does not include a placebo group 

Treatment Groups

Group I

No 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.

Group II

Experimental
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 III

Experimental
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 IV

Experimental
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.

Study Objectives

Primary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Wake Forest University Health Sciences

Winston-Salem, United StatesOpen Wake Forest University Health Sciences in Google Maps
CompletedOne Study Center