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Integrating Targeted MedlinePlus Health Prescriptions Into Clinic Practice Workflow

Obesity Clinical Trial

Official title:
Integrating Targeted MedlinePlus Health Prescriptions Into Clinic Practice Workflow

Clinical Trial Summary

The specific aim of this proposed project is to implement a standard process for integrating MedlinePlus health information prescriptions into the clinic workflow.

Hypothesis 1: Individuals in the intervention group who receive tailored email health information with provider selected MedlinePlus links and added commentary for patient specific conditions will be more likely to seek information / use MedlinePlus compared with individuals in the control group.

Hypothesis 2: Individuals in the intervention group who receive tailored email health information with provider selected MedlinePlus links and added commentary for patient specific conditions will be more satisfied with the information received compared with individuals in the control group.

Clinical Trial Description

Providing patient education in an outpatient practice can be challenging in part due to the variety of patient medical conditions and the quantity of materials needed. Increasingly, electronic resources such as those found on the internet have the potential to provide easily accessible needed information. However, clinicians do not have the time to assemble a list of websites for their patients and even if they did, the quality of information varies greatly and would require close screening. MedlinePlus is a free National Library of Medicine sponsored website that features health information on hundreds of conditions with all information carefully screened for quality standards by expert librarians. We will conduct a pilot study to seamlessly integrate provider-customized MedlinePlus health education prescriptions for specific conditions into the normal clinic workflow to motivate patients to access and expand their use of MedlinePlus to benefit their health. As HIV prevention/education is very important, we will include the HIV clinic as well as a general internal medicine clinic. ;

Study Design

Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label

Related Conditions & MeSH terms

  • Allergic Rhinitis
  • Anxiety
  • Asthma
  • Back Pain
  • Benign Prostatic Hypertrophy
  • Bursitis
  • Communicable Diseases
  • Depression
  • Diabetes Mellitus
  • Enuresis
  • Esophageal Reflux
  • Gastroesophageal Reflux
  • HIV Infections
  • Hyperlipidemia
  • Hyperlipidemias
  • Hypertension
  • Hypertrophy
  • Infection
  • Insomnia
  • Irritable Bowel Syndrome
  • Obesity
  • Osteoporosis
  • Osteoporosis (Senile)
  • Prostatic Hyperplasia
  • Rhinitis
  • Rhinitis, Allergic
  • Shoulder Pain
  • Sinusitis
  • Symptomatic Menopause
  • Urinary Incontinence
  • Urinary Tract Infection
  • Urinary Tract Infections
  • Vaginitis
Clinical Trial Details
NCT number NCT00634608
Study type Interventional
Source University of Missouri-Columbia
Contact
Status Completed
Phase N/A
Start date February 2008
Completion date September 2009
View Details
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