CClinicalTrials.gg
CompletedNCT06792890AIScribe RCTUpdated Apr 24, 2026Results posted

A Randomized Controlled Trial of Ambient Artificial Intelligence Scribe Technologies

An interventional study of Use Nabla AI Scribe tool provided and Use AI Scribe tool provided by Vendor B in Physician Workflow and Artificial Intelligence (AI), sponsored by University of California, Los Angeles. Completed at 1 site in United States. Per ClinicalTrials.gov, last updated 2026-04-24.

Sponsored by University of California, Los Angeles · Not applicable, Interventional, and Health services research

Phase
Not applicable
Study type
Interventional
Enrollment
238
Allocation
Randomized
Sex
All
01

Study summary

This is a three-arm pragmatic RCT of 238 outpatient physicians at a large academic health system, randomized 1:1:1 to one of two AI scribe tools or a usual-care control group. The two-month study will observe and compare the effects of each tool prior to system-wide roll out of selected tool (anticipated Spring 2025). We will use covariate-constrained randomization to balance the arms in terms of physician baseline time in notes, survey-measured level of burnout, and clinic days per week.

The primary purpose of the initiative is to improve quality, efficiency, and business operations at University of California, Los Angeles (UCLA) Health, and this initiative is not being done for research purposes. The results of this operational initiative will inform the widespread roll out of AI scribe tools across all providers within the UCLA Health System. Nevertheless, the UCLA study team plans to rigorously examine and publish the impact of this intervention across the health system, which is why the study team pre-registered the initiative.

Read the detailed description

This study will assess operational-oriented outcomes across all groups. Notably, all groups will eventually receive all interventions over time in this observational study of a randomized roll out of a QI initiative. Moreover, the primary purpose of this initiative is operational. In other words, based on the results of this initiative, one of these tools will be eventually selected and operationalized widely across the health system.

Enrolled participants are randomized to one of three groups. Randomization was needed to overcome secular trends, seasonal and holiday effects in December, and other factors confounding the relationship between exposure to the AI tools and the outcomes.

The primary aim of this study is to evaluate the impact of two ambient AI scribe technologies on clinician change from baseline time spent on EHR documentation, comparing each scribe to a control group. Secondary objectives include assessing the AI scribes' impact on clinician metrics such as burnout, physician satisfaction, and productivity. Additionally, the study team intends to perform an economic evaluation analysis of the tools to guide business decision making. The study team will also analyze physician reported effects of the AI tools on patient safety, equity, and any unintended consequences of the initiative.

02

Conditions studied

  • Physician Workflow
  • Artificial Intelligence (AI)

Keywords

  • Artificial Intelligence Scribe
  • Randomized Controlled Trial
  • Documentation Efficiency
  • Physician Burnout
03

In context

Lead sponsor

University of California, Los Angeles is the lead sponsor of 1,142 studies on the registry; 192 are open to participants now.

Of its 91 completed or terminated interventional studies of FDA-regulated products, 66 (73%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Ambulatory care physicians within the UCLA Health system who held at least one half-day of clinic per week

Exclusion criteria

Exclusion Criteria:

  • Trainee providers (e.g., residents, medical students) and allied healthcare professionals (e.g., RNs, PAs)
  • Attendings who work exclusively with trainees
05

Study design

Phase
Not applicable
Primary purpose
Health services research
Allocation
Randomized
Intervention model
Single group
Masking
Single (Participant)
Enrollment
238 participants (actual)

Study arms

  • Other
    Nabla, Vendor of virtual AI scribe technology

    Participants in this arm will utilize AI scribe tools from Nabla and will continue their usual clinical documentation processes, supported by the scribe software, which integrates with the EHR and automatically adds the generated text to the note. The Nabla AI scribe tool is transcriptional and does not provide clinical decision support.

    Other: Use Nabla AI Scribe tool provided

  • Other
    Vendor B of virtual AI scribe technology

    Participants in this arm will utilize AI scribe tools from Vendor B and will continue their usual clinical documentation processes, supported by the scribe software, which integrates with the EHR and automatically adds the generated text to the note. The AI scribe tool is transcriptional and does not provide clinical decision support.

    Other: Use AI Scribe tool provided by Vendor B

  • No intervention
    No Scribe

    Participants in this arm will not have access to AI scribe tools and will continue their usual clinical documentation processes

Interventions

  • OtherUse Nabla AI Scribe tool provided

    AI Scribe technologies capture physician-patient conversations to create a transcript, then summarize the transcript in the form of a clinical notes. These tools are integrated into the EHR and automatically adds the generated text to the provider note. All physicians must inform patients about the recording and obtain their verbal consent, and instances of patients declining to consent are tracked. Nabla leverages its proprietary speech-to-text to transform the conversation into a written context, combined with HIPAA compliant Large Language Models (LLM) like Azure OpenAI's GPT-4. Nabla does not store any audio.

  • OtherUse AI Scribe tool provided by Vendor B

    AI Scribe technologies capture physician-patient conversations to create a transcript, then summarize the transcript in the form of a clinical notes. These tools are integrated into the EHR and automatically adds the generated text to the provider note. All physicians must inform patients about the recording and obtain their verbal consent, and instances of patients declining to consent are tracked.

06

What researchers measure

Primary outcomes

  1. Change in the Time in Notes Per Note

    The primary outcome measure is the change in provider mean time in notes per note in the second month of the trial from the providers baseline mean time in notes per note for the six months prior to enrollment. This change will be computed on the natural log scale. No patient level information will be collected for this outcome measure.

    Time frame: Study month 2

Secondary outcomes

  1. Provider Burnout Score

    The Mini Z 2.0 Survey is a validated 10-item instrument designed to measure key factors influencing workplace satisfaction and burnout among healthcare professionals. Each item is scored on a Likert scale (1-5), with higher scores generally indicating more positive outcomes - greater job satisfaction, sufficiency of time for electronic medical record documentation, and lower levels of stress. For negatively framed items (e.g., stress due to the job or frustration with the electronic medical record), higher scores indicate lower levels of dissatisfaction. The total score ranges from 10 to 50, with scores ≥40 representing a joyful workplace. No patient level information will be collected for this outcome measure.

    Time frame: Study month 2

  2. Provider Task Load Score

    Provider task load adapted from the NASA Task Load Index (TLX), a validated tool for assessing perceived workload across six sub-scales: mental demand, physical demand, temporal demand, performance, effort, and frustration. For this study, we adapted the TLX to focus on note-writing workload, including four sub-scales (mental demand, temporal demand, physical demand, and effort) as done previously. Each sub-scale is rated from 0 (low task load) to 100 (high task load) and summed together for a total score scale of 0 (low task load) to 400 (high task load), lower is better. No patient level information will be collected for this outcome measure.

    Time frame: Study month 2

  3. Provider Professional Fulfillment

    The Professional Fulfillment Index (PFI) is a validated 16-item instrument that uses a 5-point Likert scale (0-4) to measure professional fulfillment, work exhaustion, and interpersonal disengagement. For this study, we utilize the 4-item work exhaustion subscale which is a mean of the 4-items within that subscale, where a low score (0) indicates a lower level of exhaustion and a high (4) score indicates greater level of exhaustion. No patient level information will be collected for this outcome measure.

    Time frame: Study month 2

  4. Number of Physicians Who Are Considered Detractors, Passive, or Promoters

    Self-reported satisfaction survey that asks physicians to consider note accuracy, patient safety, equity, and other potential unintended consequences and rate their overall likelihood to recommend use of the tool on a 1-10 scale. Higher scores (10) indicate greater satisfaction and likelihood to recommend, whereas lower scores (1) indicate dissatisfaction and unlikelihood to recommend. Providers are grouped as "Promoters" if they respond 9-10, "Passive" if they respond 7-8, and "Detractors" if they respond with a value less than or equal to 6. This grouping matches commonly accepted "Net Promoter Score" groupings. No patient level information will be collected for this outcome measure.

    Time frame: Study month 2

  5. Change in Provider RVU

    The study team will use physician-level billing information via RVU to determine their change in productivity from a retrospective baseline 6 months prior to enrollment. No patient level information will be collected for this outcome measure.

    Time frame: Study month 2

  6. Change in EHR Signal (Activity) Data - Pajama Time

    We will examine change from a retrospective baseline 6 months prior to enrollment in Signal metrics including pajama time per scheduled day. Using this data will determine how a providers time is utilized in the EHR. No patient level information will be collected for this outcome measure.

    Time frame: Study month 2

  7. Change in EHR Signal (Activity) Data - Time Outside Scheduled Hours

    We will examine change from a retrospective baseline 6 months prior to enrollment in Signal metrics including time outside scheduled hours per scheduled day. Using this data will determine how a providers time is utilized in the EHR. No patient level information will be collected for this outcome measure.

    Time frame: Study month 2

  8. Change in EHR Signal (Activity) Data - Time on Unscheduled Days

    We will examine change from a retrospective baseline 6 months prior to enrollment in Signal metrics including time spent in the system on unscheduled days where . Using this data will determine how a providers time is utilized in the EHR. No patient level information will be collected for this outcome measure.

    Time frame: Study month 2

07

Results

Posted Apr 24, 2026

Participant flow

Participant flow — Overall Study
MilestoneNabla, Vendor of Virtual AI Scribe TechnologyVendor B of Virtual AI Scribe TechnologyNo Scribe
Started797980
Completed797980
Not completed000

Outcome measures

PrimaryChange in the Time in Notes Per Note

The primary outcome measure is the change in provider mean time in notes per note in the second month of the trial from the providers baseline mean time in notes per note for the six months prior to enrollment. This change will be computed on the natural log scale. No patient level information will be collected for this outcome measure.

Time frame:
Study month 2
Reported as:
Mean · ln(minutes per note)
Change in the Time in Notes Per Note
ln(minutes per note)Nabla, Vendor of Virtual AI Scribe TechnologyVendor B of Virtual AI Scribe TechnologyNo Scribe
Change in the Time in Notes Per Note-0.85 ± 3.49-0.46 ± 1.16-0.29 ± 1.37
SecondaryProvider Burnout Score

The Mini Z 2.0 Survey is a validated 10-item instrument designed to measure key factors influencing workplace satisfaction and burnout among healthcare professionals. Each item is scored on a Likert scale (1-5), with higher scores generally indicating more positive outcomes - greater job satisfaction, sufficiency of time for electronic medical record documentation, and lower levels of stress. For negatively framed items (e.g., stress due to the job or frustration with the electronic medical record), higher scores indicate lower levels of dissatisfaction. The total score ranges from 10 to 50, with scores ≥40 representing a joyful workplace. No patient level information will be collected for this outcome measure.

Time frame:
Study month 2
Reported as:
Mean · score on a scale
Provider Burnout Score
score on a scaleNabla, Vendor of Virtual AI Scribe TechnologyVendor B of Virtual AI Scribe TechnologyNo Scribe
Provider Burnout Score30.43 ± 6.1131.25 ± 5.6529.30 ± 6.46
SecondaryProvider Task Load Score

Provider task load adapted from the NASA Task Load Index (TLX), a validated tool for assessing perceived workload across six sub-scales: mental demand, physical demand, temporal demand, performance, effort, and frustration. For this study, we adapted the TLX to focus on note-writing workload, including four sub-scales (mental demand, temporal demand, physical demand, and effort) as done previously. Each sub-scale is rated from 0 (low task load) to 100 (high task load) and summed together for a total score scale of 0 (low task load) to 400 (high task load), lower is better. No patient level information will be collected for this outcome measure.

Time frame:
Study month 2
Reported as:
Mean · score on a scale
Provider Task Load Score
score on a scaleNabla, Vendor of Virtual AI Scribe TechnologyVendor B of Virtual AI Scribe TechnologyNo Scribe
Provider Task Load Score56.74 ± 24.1150.33 ± 22.2960.48 ± 20.94
SecondaryProvider Professional Fulfillment

The Professional Fulfillment Index (PFI) is a validated 16-item instrument that uses a 5-point Likert scale (0-4) to measure professional fulfillment, work exhaustion, and interpersonal disengagement. For this study, we utilize the 4-item work exhaustion subscale which is a mean of the 4-items within that subscale, where a low score (0) indicates a lower level of exhaustion and a high (4) score indicates greater level of exhaustion. No patient level information will be collected for this outcome measure.

Time frame:
Study month 2
Reported as:
Mean · score on a scale
Provider Professional Fulfillment
score on a scaleNabla, Vendor of Virtual AI Scribe TechnologyVendor B of Virtual AI Scribe TechnologyNo Scribe
Provider Professional Fulfillment1.67 ± 0.901.51 ± 0.771.82 ± 0.80
SecondaryNumber of Physicians Who Are Considered Detractors, Passive, or Promoters

Self-reported satisfaction survey that asks physicians to consider note accuracy, patient safety, equity, and other potential unintended consequences and rate their overall likelihood to recommend use of the tool on a 1-10 scale. Higher scores (10) indicate greater satisfaction and likelihood to recommend, whereas lower scores (1) indicate dissatisfaction and unlikelihood to recommend. Providers are grouped as "Promoters" if they respond 9-10, "Passive" if they respond 7-8, and "Detractors" if they respond with a value less than or equal to 6. This grouping matches commonly accepted "Net Promoter Score" groupings. No patient level information will be collected for this outcome measure.

Time frame:
Study month 2
Reported as:
Count of participants · Participants
Number of Physicians Who Are Considered Detractors, Passive, or Promoters
ParticipantsNabla, Vendor of Virtual AI Scribe TechnologyVendor B of Virtual AI Scribe Technology
Detractor (<=6)2521
Passive (7-8)1715
Promoter (9-10)2330
SecondaryChange in Provider RVU

The study team will use physician-level billing information via RVU to determine their change in productivity from a retrospective baseline 6 months prior to enrollment. No patient level information will be collected for this outcome measure.

Time frame:
Study month 2
Reported as:
Mean · monthly work RVU
Change in Provider RVU
monthly work RVUNabla, Vendor of Virtual AI Scribe TechnologyVendor B of Virtual AI Scribe TechnologyNo Scribe
Change in Provider RVU-58.66 ± 132.93-13.89 ± 151.30-30.69 ± 155.98
SecondaryChange in EHR Signal (Activity) Data - Pajama Time

We will examine change from a retrospective baseline 6 months prior to enrollment in Signal metrics including pajama time per scheduled day. Using this data will determine how a providers time is utilized in the EHR. No patient level information will be collected for this outcome measure.

Time frame:
Study month 2
Reported as:
Mean · minutes/day
Change in EHR Signal (Activity) Data - Pajama Time
minutes/dayNabla, Vendor of Virtual AI Scribe TechnologyVendor B of Virtual AI Scribe TechnologyNo Scribe
Change in EHR Signal (Activity) Data - Pajama Time1.62 ± 24.920.33 ± 29.24-3.71 ± 19.63
SecondaryChange in EHR Signal (Activity) Data - Time Outside Scheduled Hours

We will examine change from a retrospective baseline 6 months prior to enrollment in Signal metrics including time outside scheduled hours per scheduled day. Using this data will determine how a providers time is utilized in the EHR. No patient level information will be collected for this outcome measure.

Time frame:
Study month 2
Reported as:
Mean · minutes/day
Change in EHR Signal (Activity) Data - Time Outside Scheduled Hours
minutes/dayNabla, Vendor of Virtual AI Scribe TechnologyVendor B of Virtual AI Scribe TechnologyNo Scribe
Change in EHR Signal (Activity) Data - Time Outside Scheduled Hours-5.31 ± 16.84-1.70 ± 11.42-1.43 ± 12.36
SecondaryChange in EHR Signal (Activity) Data - Time on Unscheduled Days

We will examine change from a retrospective baseline 6 months prior to enrollment in Signal metrics including time spent in the system on unscheduled days where . Using this data will determine how a providers time is utilized in the EHR. No patient level information will be collected for this outcome measure.

Time frame:
Study month 2
Reported as:
Mean · minutes/day
Change in EHR Signal (Activity) Data - Time on Unscheduled Days
minutes/dayNabla, Vendor of Virtual AI Scribe TechnologyVendor B of Virtual AI Scribe TechnologyNo Scribe
Change in EHR Signal (Activity) Data - Time on Unscheduled Days-6.63 ± 23.891.51 ± 26.12-3.38 ± 19.61

Adverse events

Collected over From the time the scribe was enabled for providers (study start date) until completion of the post-trial survey (study completion date), up to 72 days. Non-serious events are listed at a 5% frequency threshold.

Adverse event summary by group
GroupDeathsSeriousOther
Nabla, Vendor of Virtual AI Scribe Technology0/79 (0%)0/79 (0%)0/79 (0%)
Vendor B of Virtual AI Scribe Technology0/79 (0%)0/79 (0%)0/79 (0%)
No Scribe0/80 (0%)0/80 (0%)0/80 (0%)

Baseline characteristics

Age, Customized
Age, Customized(Participants)Nabla, Vendor of Virtual AI Scribe TechnologyVendor B of Virtual AI Scribe TechnologyNo ScribeTotal
Age — Between 25 and 341281737
Age — Between 35 and 44353739111
Age — Between 45 and 5421241459
Age — Between 55 and 6464717
Age — >=650314
Age — Prefer not to answer53210
Sex/Gender, Customized
Sex/Gender, Customized(Participants)Nabla, Vendor of Virtual AI Scribe TechnologyVendor B of Virtual AI Scribe TechnologyNo ScribeTotal
Sex — Male22313487
Sex — Female554544144
Sex — Prefer not to answer2327
Ethnicity (NIH/OMB)
Ethnicity (NIH/OMB)(Participants)Nabla, Vendor of Virtual AI Scribe TechnologyVendor B of Virtual AI Scribe TechnologyNo ScribeTotal
Hispanic or Latino57618
Not Hispanic or Latino666870204
Unknown or Not Reported84416
Race/Ethnicity, Customized
Race/Ethnicity, Customized(Participants)Nabla, Vendor of Virtual AI Scribe TechnologyVendor B of Virtual AI Scribe TechnologyNo ScribeTotal
Race — Asian33343198
Race — Black0235
Race — White25312884
Race — Multiple/Other761023
Race — Prefer not to answer146828
Region of Enrollment
Region of Enrollment(Participants)Nabla, Vendor of Virtual AI Scribe TechnologyVendor B of Virtual AI Scribe TechnologyNo ScribeTotal
United States797979237
Specialty
Specialty(Participants)Nabla, Vendor of Virtual AI Scribe TechnologyVendor B of Virtual AI Scribe TechnologyNo ScribeTotal
Primary Care373430101
Medical Specialty33283899
Surgical Specialty9171238
Time-in-note
Time-in-note(minutes per note)Nabla, Vendor of Virtual AI Scribe TechnologyVendor B of Virtual AI Scribe TechnologyNo ScribeTotal
Median4.78 (2.80 to 6.78)4.38 (3.43 to 6.05)5.37 (3.20 to 7.52)4.58 (3.19 to 7.31)
Single-item burnout
Single-item burnout(units on a scale)Nabla, Vendor of Virtual AI Scribe TechnologyVendor B of Virtual AI Scribe TechnologyNo ScribeTotal
Mean3.49 ± 0.813.49 ± 0.773.50 ± 0.783.50 ± 0.78

1 further baseline measures are reported on the registry.

08

Study locations

1 site
  • UCLA Health System
    Los Angeles, California 90024, United States
09

References and documents

Publications

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  • Gianfrancesco MA, Tamang S, Yazdany J, Schmajuk G. Potential Biases in Machine Learning Algorithms Using Electronic Health Record Data. JAMA Intern Med. 2018 Nov 1;178(11):1544-1547. doi: 10.1001/jamainternmed.2018.3763. PubMed 30128552 ↗
  • Linzer M, McLoughlin C, Poplau S, Goelz E, Brown R, Sinsky C; AMA-Hennepin Health System (HHS) burnout reduction writing team. The Mini Z Worklife and Burnout Reduction Instrument: Psychometrics and Clinical Implications. J Gen Intern Med. 2022 Aug;37(11):2876-2878. doi: 10.1007/s11606-021-07278-3. Epub 2022 Jan 19. No abstract available. PubMed 35048290 ↗
  • Trockel M, Bohman B, Lesure E, Hamidi MS, Welle D, Roberts L, Shanafelt T. A Brief Instrument to Assess Both Burnout and Professional Fulfillment in Physicians: Reliability and Validity, Including Correlation with Self-Reported Medical Errors, in a Sample of Resident and Practicing Physicians. Acad Psychiatry. 2018 Feb;42(1):11-24. doi: 10.1007/s40596-017-0849-3. Epub 2017 Dec 1. PubMed 29196982 ↗
  • Garcia P, Ma SP, Shah S, Smith M, Jeong Y, Devon-Sand A, Tai-Seale M, Takazawa K, Clutter D, Vogt K, Lugtu C, Rojo M, Lin S, Shanafelt T, Pfeffer MA, Sharp C. Artificial Intelligence-Generated Draft Replies to Patient Inbox Messages. JAMA Netw Open. 2024 Mar 4;7(3):e243201. doi: 10.1001/jamanetworkopen.2024.3201. PubMed 38506805 ↗
  • Cruz Rivera S, Liu X, Chan AW, Denniston AK, Calvert MJ; SPIRIT-AI and CONSORT-AI Working Group; SPIRIT-AI and CONSORT-AI Steering Group; SPIRIT-AI and CONSORT-AI Consensus Group. Guidelines for clinical trial protocols for interventions involving artificial intelligence: the SPIRIT-AI extension. Nat Med. 2020 Sep;26(9):1351-1363. doi: 10.1038/s41591-020-1037-7. Epub 2020 Sep 9. PubMed 32908284 ↗
  • McCoy LG, Manrai AK, Rodman A. Large Language Models and the Degradation of the Medical Record. N Engl J Med. 2024 Oct 31;391(17):1561-1564. doi: 10.1056/NEJMp2405999. Epub 2024 Oct 26. No abstract available. PubMed 39465898 ↗
  • Hendrix N, Veenstra DL, Cheng M, Anderson NC, Verguet S. Assessing the Economic Value of Clinical Artificial Intelligence: Challenges and Opportunities. Value Health. 2022 Mar;25(3):331-339. doi: 10.1016/j.jval.2021.08.015. Epub 2021 Oct 9. PubMed 35227443 ↗
  • Rotenstein L, Melnick ER, Iannaccone C, Zhang J, Mugal A, Lipsitz SR, Healey MJ, Holland C, Snyder R, Sinsky CA, Ting D, Bates DW. Virtual Scribes and Physician Time Spent on Electronic Health Records. JAMA Netw Open. 2024 May 1;7(5):e2413140. doi: 10.1001/jamanetworkopen.2024.13140. PubMed 38787556 ↗
  • Cao DY, Silkey JR, Decker MC, Wanat KA. Artificial intelligence-driven digital scribes in clinical documentation: Pilot study assessing the impact on dermatologist workflow and patient encounters. JAAD Int. 2024 Feb 20;15:149-151. doi: 10.1016/j.jdin.2024.02.009. eCollection 2024 Jun. No abstract available. PubMed 38571698 ↗
  • Owens LM, Wilda JJ, Grifka R, Westendorp J, Fletcher JJ. Effect of Ambient Voice Technology, Natural Language Processing, and Artificial Intelligence on the Patient-Physician Relationship. Appl Clin Inform. 2024 Aug;15(4):660-667. doi: 10.1055/a-2337-4739. Epub 2024 Jun 4. PubMed 38834180 ↗
  • Haberle T, Cleveland C, Snow GL, Barber C, Stookey N, Thornock C, Younger L, Mullahkhel B, Ize-Ludlow D. The impact of nuance DAX ambient listening AI documentation: a cohort study. J Am Med Inform Assoc. 2024 Apr 3;31(4):975-979. doi: 10.1093/jamia/ocae022. PubMed 38345343 ↗
  • Liu TL, Hetherington TC, Stephens C, McWilliams A, Dharod A, Carroll T, Cleveland JA. AI-Powered Clinical Documentation and Clinicians' Electronic Health Record Experience: A Nonrandomized Clinical Trial. JAMA Netw Open. 2024 Sep 3;7(9):e2432460. doi: 10.1001/jamanetworkopen.2024.32460. PubMed 39240568 ↗
  • Blackley SV, Huynh J, Wang L, Korach Z, Zhou L. Speech recognition for clinical documentation from 1990 to 2018: a systematic review. J Am Med Inform Assoc. 2019 Apr 1;26(4):324-338. doi: 10.1093/jamia/ocy179. PubMed 30753666 ↗
  • Heckman J, Mukamal KJ, Christensen A, Reynolds EE. Medical Scribes, Provider and Patient Experience, and Patient Throughput: a Trial in an Academic General Internal Medicine Practice. J Gen Intern Med. 2020 Mar;35(3):770-774. doi: 10.1007/s11606-019-05352-5. Epub 2019 Dec 5. PubMed 31808131 ↗
  • Bates DW, Landman AB. Use of Medical Scribes to Reduce Documentation Burden: Are They Where We Need to Go With Clinical Documentation? JAMA Intern Med. 2018 Nov 1;178(11):1472-1473. doi: 10.1001/jamainternmed.2018.3945. No abstract available. PubMed 30242315 ↗
  • Mishra P, Kiang JC, Grant RW. Association of Medical Scribes in Primary Care With Physician Workflow and Patient Experience. JAMA Intern Med. 2018 Nov 1;178(11):1467-1472. doi: 10.1001/jamainternmed.2018.3956. PubMed 30242380 ↗
  • Steinkamp J, Kantrowitz JJ, Airan-Javia S. Prevalence and Sources of Duplicate Information in the Electronic Medical Record. JAMA Netw Open. 2022 Sep 1;5(9):e2233348. doi: 10.1001/jamanetworkopen.2022.33348. PubMed 36156143 ↗
  • Sinsky C, Colligan L, Li L, Prgomet M, Reynolds S, Goeders L, Westbrook J, Tutty M, Blike G. Allocation of Physician Time in Ambulatory Practice: A Time and Motion Study in 4 Specialties. Ann Intern Med. 2016 Dec 6;165(11):753-760. doi: 10.7326/M16-0961. Epub 2016 Sep 6. PubMed 27595430 ↗
  • Guille C, Sen S. Burnout, Depression, and Diminished Well-Being among Physicians. N Engl J Med. 2024 Oct 24;391(16):1519-1527. doi: 10.1056/NEJMra2302878. No abstract available. PubMed 39442042 ↗
  • Lou SS, Lew D, Harford DR, Lu C, Evanoff BA, Duncan JG, Kannampallil T. Temporal Associations Between EHR-Derived Workload, Burnout, and Errors: a Prospective Cohort Study. J Gen Intern Med. 2022 Jul;37(9):2165-2172. doi: 10.1007/s11606-022-07620-3. Epub 2022 Jun 16. PubMed 35710654 ↗
  • Moy AJ, Schwartz JM, Chen R, Sadri S, Lucas E, Cato KD, Rossetti SC. Measurement of clinical documentation burden among physicians and nurses using electronic health records: a scoping review. J Am Med Inform Assoc. 2021 Apr 23;28(5):998-1008. doi: 10.1093/jamia/ocaa325. PubMed 33434273 ↗
  • Peccoralo LA, Kaplan CA, Pietrzak RH, Charney DS, Ripp JA. The impact of time spent on the electronic health record after work and of clerical work on burnout among clinical faculty. J Am Med Inform Assoc. 2021 Apr 23;28(5):938-947. doi: 10.1093/jamia/ocaa349. PubMed 33550392 ↗
  • Lukac PJ, Turner W, Vangala S, Chin AT, Khalili J, Shih YT, Sarkisian C, Cheng EM, Mafi JN. Ambient AI Scribes in Clinical Practice: A Randomized Trial. NEJM AI. 2025 Dec;2(12):10.1056/aioa2501000. doi: 10.1056/aioa2501000. Epub 2025 Nov 26. PubMed 41497288 ↗
  • Lukac PJ, Turner W, Vangala S, Chin AT, Khalili J, Shih YT, Sarkisian C, Cheng EM, Mafi JN. A Randomized-Clinical Trial of Two Ambient Artificial Intelligence Scribes: Measuring Documentation Efficiency and Physician Burnout. medRxiv [Preprint]. 2025 Jul 11:2025.07.10.25331333. doi: 10.1101/2025.07.10.25331333. PubMed 40672471 ↗

Study documents

  • Protocol and statistical analysis plan · Jan 28, 2025

Documents are hosted by the registry — open the source record to download them.

Individual participant data

Plan to share: No

10

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 24, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
11

Registry details

Key details

Study ID
NCT06792890
Lead sponsor
University of California, Los Angeles
Responsible party
John N. Mafi, MD, MPH (Associate Professor of Medicine, University of California, Los Angeles) — Principal investigator
First posted
Jan 27, 2025
Start date
Nov 4, 2024
Primary completion
Jan 3, 2025
Completion
Jan 15, 2025
Results posted
Apr 24, 2026
Last update
Apr 24, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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