The Development and Evaluation of an "E-Visit" Program for the Management of Acne

Mass General Brigham

Status: Completed

Conditions: Acne Vulgaris

Treatments: Other: Evisit; Other: Office visit

Study type: Interventional

Funder types: Other

Identifiers

NCT00417456

2005-P-000289

Details and patient eligibility

About

The purpose of this study is to test the efficacy, timeliness, and user satisfaction of an online "E-Visit" application that uses store-and-forward technology for acne patients requiring dermatologic care for their condition. Hypotheses:

1. That an "E-Visit" is an effective alternative to in-person clinic care for patients with mild to severe facial acne.
2. That providers and patients will be satisfied with this model.
3. That mean wait times for new and return visits will be reduced through the "E-Visit" model.
4. That this prototype for care will improve clinic workflow, offer additional patient access, and allow urgent cases to be seen earlier.

Full description

Across the United States, a geographically mal-distributed workforce of Dermatologists exists, a problem that is projected to worsen. Patient access to dermatologic care is threatened. The dermatology workforce shortage has resulted in long wait times for patients, especially new patient visits and acute care cases.

Teledermatology has received much attention as a solution to the preceding problems. Teledermatology can reduce the burden of repeat office visits in chronic conditions by facilitating care from home. In this trial, a model incorporating store-and-forward technology is tested in general clinics while its impact on clinical outcomes, satisfaction, and wait times are studied.

Comparison: After consent, study subjects are assigned a unique study number and randomly assigned to one of two groups:

Group 1- The first group of subjects will have four (4) in-office visits spaced six weeks apart.

Group 2- The second group will have four (4) "e-visits" spaced six weeks apart.

At the end of study (after completion of 5th visit overall) all participants will complete a satisfaction survey.

Enrollment: 151 patients

Sex: All

Ages: 12+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Age 12 or older
• Diagnosis of mild to severe facial acne
• Access to a credit card
• Access to an Internet connection and a computer
• Ability to image self
• MA Blue Cross/ Blue Shield Coverage

Exclusion criteria

• Non-English speaking individuals
• Patients taking Accutane for their acne
• Impaired Physical ability to image self
• Impaired Cognitive ability

Trial design

Primary purpose: Health Services Research

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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151 participants in 2 patient groups

1

Active Comparator group

Description:

Office Visits

Treatment:

Other: Office visit

2

Experimental group

Description:

Evisit

Treatment:

Other: Evisit