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AI Virtual Assistant for Surgery Patients
N/A
Waitlist Available
Led By Antonio Forte, MD, PhD
Research Sponsored by Mayo Clinic
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 12 months
Awards & highlights
No Placebo-Only Group
Summary
This trial is testing if an AI virtual assistant on mobile phones can help patients planning surgery by providing answers and information about their procedure.
Who is the study for?
This trial is for adults over 18 who are patients at the Plastic Surgery outpatient clinic of Mayo Clinic Florida. Participants need to be able to use mobile phone apps and must consent to join the study.
What is being tested?
The study is examining the long-term effects of providing plastic surgery patients with an Artificial Intelligence Virtual Assistant (AIVA) as a supplementary resource.
What are the potential side effects?
Since this trial involves a virtual assistant, there are no direct medical side effects. However, participants may experience issues related to technology use such as privacy concerns or data security risks.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 12 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~12 months
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Duration of phone call
Nature of phone call
Number of phone calls
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Subjects with virtual assistanceExperimental Treatment1 Intervention
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)
Group II: Subjects without virtual assistanceActive Control1 Intervention
Subjects receiving current standard of care for a surgical procedure within the department of plastic surgery
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Surgical treatments generally involve the physical removal, repair, or replacement of diseased or damaged tissues and organs. Common mechanisms include excision (cutting out tissue), reconstruction (repairing or reshaping tissue), and transplantation (replacing tissue or organs).
These interventions are crucial for addressing conditions that cannot be managed with medication alone. The use of supportive technologies like the Artificial Intelligence Virtual Assistant (AIVA) can significantly enhance patient outcomes by providing timely information, reminders, and emotional support, thereby improving adherence to post-operative care plans and reducing complications.
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Find a Location
Who is running the clinical trial?
Mayo ClinicLead Sponsor
3,353 Previous Clinical Trials
3,060,823 Total Patients Enrolled
13 Trials studying Surgery
7,096 Patients Enrolled for Surgery
Antonio Forte, MD, PhDPrincipal InvestigatorMayo Clinic
5 Previous Clinical Trials
870 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I am over 18 years old.
Research Study Groups:
This trial has the following groups:- Group 1: Subjects without virtual assistance
- Group 2: Subjects with virtual assistance
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.