Effectiveness of an Internet-Based Curriculum in Increasing Health Care Providers' Knowledge of Herbs and Dietary Supplements

May 23, 2012 updated by: National Library of Medicine (NLM)

Internet-Based Curriculum About Herbs and Dietary Supplements

The purpose of this study is to determine the effectiveness of four different strategies designed to improve clinicians' knowledge about herbs and dietary supplements. This study will also increase their confidence in their ability to answer patient questions about these topics.

Study hypotheses: 1) Delivery of modules over 10 weeks will lead to better educational outcomes than delivery of modules at one time. 2) The method of module delivery that directly lists the modules in an email will be associated with greater improvements in knowledge, confidence, and communication skills and greater satisfaction with the overall curriculum than methods that involve the delivery of only links to the modules in an email. 3) Active participation in a moderated mailing list will enhance outcomes and satisfaction with the curriculum more than non-participation or passive participation (reading the messages of others). 4) More positive attitudes toward the use of and greater use of computer and Internet technologies at baseline will be associated with more active participation in the mailing list; greater use of the modules delivered through links; greater improvements in knowledge, confidence, and communication; and more positive attitudes about the curriculum following participation in the study.

Study Overview

Status

Completed

Conditions

Detailed Description

As herbal medicine use becomes more popular, health care providers may find that patients are asking questions about the risks and benefits of complementary and alternative medicine (CAM) more frequently. It is important that providers have some knowledge about these therapies and are familiar with resources to which they can refer patients. This study will compare the effectiveness of four strategies used to deliver educational modules that can increase health care providers' knowledge about herbal medicine and dietary supplements.

This study will last about 10 weeks and will enroll a variety of health care providers, including physicians, physician assistants, pharmacists, dietitians, and nurses. At study entry, participants will be stratified by provider type. Participants will then be randomly assigned to 1 of 4 educational delivery strategies: delivery of educational modules all at one time directly through email, delivery of modules over 10 weeks directly through email, delivery of modules through an email message with a link to an Internet site containing all modules, or delivery of multiple emails over 10 weeks with links to an Internet site containing all modules.

Each module will begin with a brief clinical scenario followed by questions to assess knowledge, confidence about where to locate information, and the level of communication that providers have engaged in with their patients. Participants will complete questionnaires at study entry and at Week 10. The questionnaires will assess the use of and attitudes toward Internet technology, motivation for participating in the course, and knowledge, attitudes, and communication practices related to the clinical use of herbs and dietary supplements. Participants will have the opportunity to participate in a moderated mailing list where they can discuss CAM-related topics with other providers and read the discussions of others. In addition, after completing the curriculum, participants will complete questionnaires about their use of and attitudes toward the intervention they received in the study.

Study Type

Interventional

Enrollment

1500

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • North Carolina
      • Winston-Salem, North Carolina, United States, 27157
        • Northwest Area Health Education Center

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Live and work in the United States
  • Licensed to provide health care in the United States
  • Have regular access to the Internet and an e-mail address that can be checked at least twice weekly for at least 4 months
  • Willing to complete all study assessments

Exclusion Criteria:

  • Previous enrollment in this curriculum

Study Plan

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

How is the study designed?

Design Details

  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Double

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Changes in participant knowledge, confidence, and communication practices regarding herbs and dietary supplements

Secondary Outcome Measures

Outcome Measure
Impact of comfort with using technology on the primary outcomes

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Kathi Kemper, MD, Wake Forest University Health Sciences

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

February 1, 2004

Primary Completion

December 7, 2022

Study Completion

December 1, 2004

Study Registration Dates

First Submitted

May 10, 2005

First Submitted That Met QC Criteria

May 10, 2005

First Posted (Estimate)

May 11, 2005

Study Record Updates

Last Update Posted (Estimate)

May 24, 2012

Last Update Submitted That Met QC Criteria

May 23, 2012

Last Verified

August 1, 2006

More Information

Terms related to this study

Other Study ID Numbers

  • R01LM007709 (U.S. NIH Grant/Contract)

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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