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MedlinePlus Health Prescriptions: Developing a Pragmatic Approach for Clinic Use

University of Missouri (MU) logo

University of Missouri (MU)

Status

Completed

Conditions

Vertigo
Coronary Artery Disease
Tobacco Use Cessation
Migraine Disorders
Hypothyroidism
Obesity
HIV Infections
Shoulder Pain
Irritable Bowel Syndrome
Sleep Initiation and Maintenance Disorders
Osteoarthritis
Hyperlipidemia
Diarrhea
Chronic Obstructive Pulmonary Disease
Gastroesophageal Reflux
Vaginitis
Bursitis
Sinusitis
Senile Osteoporosis
Fibromyalgia
Back Pain
Urinary Tract Infection
Menopause
Diabetes Mellitus
Cough
Allergic Rhinitis
Anxiety
Smoking Cessation
Headache
Hypertension
Asthma
Influenza
Acne Vulgaris
Depression
Prostatic Hyperplasia
Urinary Incontinence
Obstructive Sleep Apnea

Treatments

Other: health information prescription

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT01050465
HHSN276200800445P

Details and patient eligibility

About

The specific aim of this proposed pilot study is to compare two standardized processes (paper and electronic) to deliver a customized MedlinePlus health information prescription.

Full description

The specific aim of this proposed pilot study is to compare two standardized processes (paper and electronic) to deliver a customized MedlinePlus health information prescription.

Primary Hypothesis. Individuals in the paper prescription group will be just as likely to seek information using MedlinePlus compared with individuals in the group who receive the same customized information through an email prescription.

Secondary Hypothesis. Individuals in the paper prescription group will be just as likely to have successful behavioral outcome measures as those in the group who receive the same customized information through an email prescription.

Enrollment

907 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  • one of the 40 target health conditions.

Exclusion Criteria

  • absence of at least one of the target 40 conditions

Trial design

907 participants in 2 patient groups

email
Active Comparator group
Description:
Patients randomized to this arm will receive an email health information prescription.
Treatment:
Other: health information prescription
paper
Active Comparator group
Description:
Patients randomized to this arm will receive a paper health information prescription.
Treatment:
Other: health information prescription

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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