The Medication Experience Study

This study is currently recruiting participants. (see Contacts and Locations)
Verified May 2014 by Wake Forest School of Medicine
Sponsor:
Information provided by (Responsible Party):
Steven R. Feldman, Wake Forest School of Medicine
ClinicalTrials.gov Identifier:
NCT01702883
First received: October 4, 2012
Last updated: May 27, 2014
Last verified: May 2014

October 4, 2012
May 27, 2014
October 2012
June 2015   (final data collection date for primary outcome measure)
The primary measure will be adherence as measured by pharmacy refills in each group. [ Time Frame: 12 months ] [ Designated as safety issue: No ]
Same as current
Complete list of historical versions of study NCT01702883 on ClinicalTrials.gov Archive Site
Not Provided
Not Provided
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The Medication Experience Study
Using an Internet Survey to Improve Patient Adherence in Chronic Disease

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

Not Provided
Interventional
Not Provided
Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Factorial Assignment
Masking: Double Blind (Subject, Investigator)
  • Hypertension
  • Elevated Cholesterol
  • Diabetes
  • Depression
Other: Internet Survey
prompt to complete internet survey
Other Name: internet surveys
  • No Intervention: Control
    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.
  • Experimental: Intervention Group A
    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.
    Intervention: Other: Internet Survey
  • Experimental: Intervention Group B
    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.
    Intervention: Other: Internet Survey
  • Experimental: Intervention Group C
    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.
    Intervention: Other: Internet Survey
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruiting
1112
September 2015
June 2015   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • 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.

Exclusion Criteria:

  • 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.
Both
18 Years and older
No
Contact: Irma M Richardson, MHA 336-716-2903 irichard@wakehealth.edu
United States
 
NCT01702883
20789
No
Steven R. Feldman, Wake Forest School of Medicine
Wake Forest School of Medicine
Not Provided
Principal Investigator: Steve R Feldman, MD, PhD Wake Forest School of Medicine
Wake Forest School of Medicine
May 2014

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP