- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00634608
Integrating Targeted MedlinePlus Health Prescriptions Into Clinic Practice Workflow
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.
Study Overview
Status
Conditions
- Depression
- HIV Infections
- Hypertension
- Obesity
- Diabetes Mellitus
- Back Pain
- Urinary Incontinence
- Irritable Bowel Syndrome
- Insomnia
- Asthma
- Anxiety
- Sinusitis
- Shoulder Pain
- Allergic Rhinitis
- Urinary Tract Infection
- Vaginitis
- Bursitis
- Hyperlipidemia
- Esophageal Reflux
- Benign Prostatic Hypertrophy
- Osteoporosis (Senile)
- Symptomatic Menopause
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Missouri
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Columbia, Missouri, United States, 65211
- University of Missouri, Department of Internal Medicine
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- To be included in the study population, patients must also be seen by their physician for one of the 21 target health conditions (Allergic Rhinitis, Asthma, Back Pain, Benign Prostatic Hypertrophy, Bursitis, Depression/Anxiety, Diabetes Mellitus, Esophageal Reflux, HIV, Hyperlipidemia, Hypertension, Insomnia, Irritable Bowel Syndrome, Obesity, Osteoporosis (senile), Shoulder Pain, Sinusitis, Symptomatic Menopause, Urinary Incontinence, Urinary Tract Infection, Vaginitis) and be willing to provide an email address.
- Patients will be included only once.
- All patients in the intervention and the control group will receive the survey.
- All physicians and staff at the Fairview Clinic and HIV Clinic will be invited to complete the physician or staff survey.
Exclusion Criteria:
- No email address
Study Plan
How is the study designed?
Design Details
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
No Intervention: Survey
Control group participants are sent a survey within one week of clinic visit
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Experimental: Health Information Prescription
Health Information Prescription is emailed to participants within 24 hours of clinic visit.
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The patient education materials will consist of approximately 21 topics representing some of the most common conditions seen at the Fairview Internal Medicine Clinic.
Twenty-one e-mails, one per topic, will be created by Fairview physicians to be distributed to selected clinic patients.
There will be a standard e-mail for each condition with a specific link to MedlinePlus.
To create the targeted health information topic email, the physician will review the information available at MedlinePlus.
The physician will then select several links of appropriate information and, using the template, will write a short annotation on each link.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
health information experiences of the patient
Time Frame: approximately one week following clinic appointment
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approximately one week following clinic appointment
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Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
clinician feedback on the health information prescription process
Time Frame: midpoint and conclusion of the study
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midpoint and conclusion of the study
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Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Robert Hodge, MD, University of Missouri-Columbia
Publications and helpful links
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Digestive System Diseases
- Pathologic Processes
- Metabolic Diseases
- Respiratory Tract Infections
- Respiratory Tract Diseases
- Urologic Diseases
- Lower Urinary Tract Symptoms
- Urological Manifestations
- Pain
- Neurologic Manifestations
- Disease Attributes
- Gastrointestinal Diseases
- Prostatic Diseases
- Joint Diseases
- Musculoskeletal Diseases
- Otorhinolaryngologic Diseases
- Urination Disorders
- Colonic Diseases, Functional
- Colonic Diseases
- Intestinal Diseases
- Pathological Conditions, Anatomical
- Bone Diseases
- Esophageal Motility Disorders
- Deglutition Disorders
- Esophageal Diseases
- Paranasal Sinus Diseases
- Nose Diseases
- Lipid Metabolism Disorders
- Arthralgia
- Dyslipidemias
- Bone Diseases, Metabolic
- Vaginal Diseases
- Urinary Incontinence
- Irritable Bowel Syndrome
- Infections
- Communicable Diseases
- Prostatic Hyperplasia
- Gastroesophageal Reflux
- Sinusitis
- Shoulder Pain
- Urinary Tract Infections
- Osteoporosis
- Vaginitis
- Hypertrophy
- Hyperlipidemias
- Bursitis
Other Study ID Numbers
- HHSN276200700263P
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
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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