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Virtual Assistant for Plastic Surgery Patients

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Mayo Clinic

Status

Not yet enrolling

Conditions

Surgery

Treatments

Other: Artificial Intelligence Virtual Assistant

Study type

Interventional

Funder types

Other

Identifiers

NCT04017351
19-001980

Details and patient eligibility

About

Researchers are trying determine the long term impact when patients have access to the artificial intelligence virtual assistant (AIVA) as a complimentary resource.

Full description

Eligible subjects will be randomized into to two groups. One group of subjects will be given access to the AIVA will be instructed to ask, at home, questions regarding the planned surgery to the AIVA application on their mobile phone. The other group will be instructed to call to the Standard of Care call center with questions related to their treatments. Researchers will follow up with all subjects from both groups for a 1 year amount of time.

Enrollment

200 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Subjects above 18 years old
  • Able to use applications on mobile phones and consent to participate
  • Adult subjects in the Plastic Surgery outpatient clinic of Mayo Clinic Florida

Exclusion criteria

-

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

200 participants in 2 patient groups

Subjects with virtual assistance
Experimental group
Description:
Subjects receiving current standard of care for a surgical procedure within the department of plastic surgery will have access to artificial intelligence virtual assistance (AIVA)
Treatment:
Other: Artificial Intelligence Virtual Assistant
Subjects without virtual assistance
No Intervention group
Description:
Subjects receiving current standard of care for a surgical procedure within the department of plastic surgery

Trial contacts and locations

1

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Central trial contact

Mauricia Buchanan, RN; Antonio Forte, MD, PhD

Data sourced from clinicaltrials.gov

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