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Behavioural Intervention

Ambient Digital Scribes for Patient and Clinician Satisfaction

N/A
Recruiting
Research Sponsored by Duke University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Patient: 18 years or older
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up through study completion, an average of 2 months
Awards & highlights
No Placebo-Only Group

Summary

This trial aims to see how using Ambient Digital Scribes, which automatically record clinical encounters and generate notes using AI, affects both patients and clinicians. The researchers anticipate that using this technology will lead to increased

Who is the study for?
This trial is for clinicians who regularly document clinical encounters and their patients. The study aims to include participants who are willing to have their consultations recorded and notes generated by AI technology. Specific eligibility criteria details were not provided.
What is being tested?
The intervention being tested is the use of Ambient Digital Scribes, an AI technology that records clinical encounters and automatically generates clinical notes, aiming to improve patient satisfaction, reduce clinician burnout, and enhance communication quality.
What are the potential side effects?
Since this trial involves non-medical technology rather than a drug or medical procedure, traditional side effects are not applicable. However, potential issues may include privacy concerns with recording conversations or inaccuracies in AI-generated notes.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
Select...
I am 18 years old or older.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~through study completion, an average of 2 months
This trial's timeline: 3 weeks for screening, Varies for treatment, and through study completion, an average of 2 months for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Patient Satisfaction
Patient-perceived clinician empathy
Secondary study objectives
Clinician Communication
Clinician Satisfaction as measured by level of burnout

Awards & Highlights

No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Trial Design

1Treatment groups
Experimental Treatment
Group I: Study population - Clinicians and PatientsExperimental Treatment1 Intervention
Clinicians will audio record 4 patient encounters on two separate days each (240 encounters).

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Who is running the clinical trial?

Duke UniversityLead Sponsor
2,463 Previous Clinical Trials
2,981,277 Total Patients Enrolled
~0 spots leftby Dec 2024
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