Clinical Trials Logo

Clinical Trial Summary

There are several benefits of over-the-counter medications, yet there is little research evaluating how to increase patient compliance when a health care provider suggests an over-the-counter (OTC) medication. We are evaluating two types of physician directions to see which increases patient compliance with OTC medications.


Clinical Trial Description

Researchers will identify a cohort of gynecologic patients presenting for annual examinations and offer participation in the study. Physician researchers will randomize patients to 2 types of physician directions about OTC medications, then follow compliance over the course of the next 7 months. A total of 123 participants in each arm will undergo recruitment, until a total of 246 participants are recruited.

Inclusion criteria include: female, non-pregnant patients presenting for annual gynecologic examinations between the ages of 19-50.

Exclusion criteria include: outside of study age range, patient taking thyroid medication, history of kidney stones, history of hypercalcemia, non-English speaking. ;


Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Single Blind (Subject), Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00439348
Study type Interventional
Source Florida Hospital
Contact
Status Completed
Phase N/A
Start date February 2007
Completion date February 2009

See also
  Status Clinical Trial Phase
Enrolling by invitation NCT05133700 - Use and Opinions of Care Home Medicines Audit Tools
Completed NCT03799367 - The Feasibility of Drug Delivery to Infants During Breastfeeding N/A