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The Medication Experience Study

Wake Forest University (WFU) logo

Wake Forest University (WFU)

Status

Completed

Conditions

Elevated Cholesterol
Hypertension
Diabetes
Depression

Treatments

Other: Internet Survey

Study type

Interventional

Funder types

Other

Identifiers

NCT01702883
IRB00020789

Details and patient eligibility

About

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

Enrollment

186 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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.

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Factorial Assignment

Masking

Double Blind

186 participants in 4 patient groups

Control
No Intervention group
Description:
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.
Intervention Group A
Experimental group
Description:
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.
Treatment:
Other: Internet Survey
Intervention Group B
Experimental group
Description:
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.
Treatment:
Other: Internet Survey
Intervention Group C
Experimental group
Description:
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.
Treatment:
Other: Internet Survey

Trial documents
1

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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