ClinicalTrials.gg
Enrolling by invitationNCT07475104Updated May 4, 2026

Redesigning Surgical Care for Patients in Wisconsin

An interventional study of Education Specialist Delivered Training and Automated Training in Communication, Surgery and Shared Decision Making, sponsored by University of Wisconsin, Madison. Enrolling by invitation at 2 sites in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-05-04.

Sponsored by University of Wisconsin, Madison · Not applicable, Interventional, and Health services research

Phase
Not applicable
Study type
Interventional
Enrollment
660
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

This study evaluates strategies to train surgeons to use Better Conversations, an evidence-based communication framework designed to improve informed consent by helping patients understand the goals of surgery, the downsides of treatment, and what to expect. Better Conversations supports deliberation, patient preparation, and alignment of decisions with patient goals, addressing known shortcomings in traditional informed consent.

The purpose of this study is to compare two methods of surgeon training: (1) training delivered by an education specialist using audit and feedback, and (2) training supported by computerized automation that identifies elements of Better Conversations in de-identified transcripts of surgical consultations. The central question is whether the automated training program is non-inferior to the specialist-delivered program.

Approximately 60 surgeons from two academic health systems will be randomized to one of these training approaches. Each surgeon will complete a didactic session, have outpatient surgical consultations audio-recorded for feedback, and complete assessment recordings after training. Patients of enrolled surgeons will complete surveys before and after their surgeon's training to evaluate patient-reported communication outcomes.

Findings from this study will assess the effectiveness, feasibility, and acceptability of automated training and support the development of a larger pragmatic study to evaluate the broader effects of Better Conversations on patient outcomes.

Read the detailed description

This study evaluates two training strategies to help surgeons use Better Conversations, an evidence-based communication framework that improves informed consent by supporting patient understanding, deliberation, and preparation for surgery. Prior work by the investigative team shows that Better Conversations addresses shortcomings in traditional consent practices, aligns with quality improvement standards, and is well-received by surgeons and patients.

This is a non-inferiority trial comparing (1) audit-and-feedback training delivered by an education specialist and (2) an automated training approach that uses natural language processing and active machine learning to identify key elements of Better Conversations in de-identified transcripts of surgical consultations. Automated output is reviewed and finalized by the education specialist before being shared with surgeons. The hypothesis is that automated training will be non-inferior to specialist-delivered training, with a 5% non-inferiority margin.

The study also evaluates feasibility and acceptability of training a large number of surgeons across two institutions. Feasibility is defined as training at least 80% of surgeons to competence. Acceptability will be assessed using surgeon surveys and exit interviews, and patient-reported outcomes. Patients will complete validated surveys (Feeling Heard and Understood; CAHPS Surgical Care items) before and after their surgeon's training. A subset of patients will participate in interviews regarding their consultation experience. A separate group of patients will consent to have their consultations audio recorded solely for surgeon training or assessment purposes.

Sixty surgeons from UW Health and the Medical College of Wisconsin will be randomized, stratified by site, to one of the two training groups. All surgeons will begin with a 30-minute didactic session, followed by 10 training recordings with corresponding feedback, and 5-7 assessment recordings used to evaluate competence. Consultations will be audio recorded, transcribed, and de-identified prior to feedback and analysis. Competence will be evaluated using a standardized adherence checklist developed by the study team, assessing both the presence and quality of required communication elements.

This study will generate estimates of within- and between-surgeon variation in communication performance and patient-reported outcomes. These data will inform analytic planning and power calculations for a future pragmatic trial examining the broader impact of Better Conversations on patient decision making, satisfaction, and health outcomes.

02

Conditions studied

  • Communication
  • Surgery
  • Shared Decision Making

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Keywords

  • informed consent
  • health literacy
  • surgical training
  • shared decision making
  • surgical communication
03

In context

Communication

719 studies on the registry are indexed under Communication; 159 are open to participants now.

This study's planned enrollment of 660 is above the median of 144 across 571 interventional studies indexed under Communication.

Browse Communication studies →

Lead sponsor

University of Wisconsin, Madison is the lead sponsor of 1,188 studies on the registry; 181 are open to participants now.

Of its 157 completed or terminated interventional studies of FDA-regulated products, 118 (75%) have results posted.

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

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Eligibility criteria

Inclusion Criteria (Surgeons):

  • Surgeons who work in the University of Wisconsin-Madison and Medical College of Wisconsin who have an outpatient surgical clinic and treat adult patients at UW Health or Froedtert Hospital and MCW

Inclusion Criteria (Patients):

  • Adult patients with decision making capacity
  • Presenting to an enrolled surgeon's clinic with a surgical problem to discuss treatment

Exclusion Criteria (Surgeons):

  • Surgeons who solely treat minors (under age 18), i.e., pediatric surgeons, will be excluded from this study, but training will be made available to them outside of this study.
  • Surgeons at UWH who have previously been trained to use Better Conversations (25 surgeons) are excluded.

Exclusion Criteria (Patients):

  • Adult patients who do not have decision making capacity will be excluded.
  • Individuals who do not speak English will be excluded.
05

Study design

Phase
Not applicable
Primary purpose
Health services research
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Triple (Participant, Investigator, Outcomes assessor)
Enrollment
660 participants (estimated)

Study arms

  • Active comparator
    Control - Education Specialist Delivered Training

    Surgeons receive standard audit-and-feedback training delivered by an education specialist, including a brief didactic session and feedback on 10 de-identified outpatient consultations. Five additional recordings are used to assess performance with an adherence checklist.

    Behavioral: Education Specialist Delivered Training

  • Experimental
    Intervention A - Automated Training

    Surgeons receive automated audit-and-feedback training. De-identified transcripts from 10 consultations are processed with previously developed natural language processing, and an education specialist reviews and edits the automated output. Five additional recordings are assessed using the same checklist.

    Behavioral: Automated Training

  • Experimental
    Intervention B - Automated Training with Disclosure Messaging

    Identical to Intervention A with the addition that surgeons receive intermittent disclosure messages indicating that some feedback is computer-generated. Assessment and scoring procedures match the other arms and use the adherence checklist with a competence threshold.

    Behavioral: Automated Training

Interventions

  • BehavioralEducation Specialist Delivered Training

    Training in the Better Conversations framework delivered by an education specialist, including a brief didactic session and audit-and-feedback based on 10 de-identified outpatient consultations, followed by assessment using five additional recordings scored with an adherence checklist.

    Also known as: Better Conversations, Better Conversations for Better Informed Consent

  • BehavioralAutomated Training

    Training in the Better Conversations framework supported by computerized automation. Procedures match the education-specialist approach (didactic session; 10 training recordings; 5-7 assessment recordings). For each training consultation, the de-identified transcript is processed using previously developed natural language processing with active/supervised machine learning to identify elements of Better Conversations that are present or absent and common errors. An education specialist reviews and edits the automated output and emails feedback and a score sheet within one week using the same standardized format. In one half of the automated-training arm, surgeons also receive intermittent disclosure messages indicating that some feedback is computer-generated.

    Also known as: Better Conversations, Better Conversations for Better Informed Consent

06

What researchers measure

Primary outcomes

  1. Percentage of surgeons trained to competence

    Competence is assessed using the established 10-item adherence checklist, yielding a total possible score ranging from 0 to 10, applied to the five assessment audio recordings obtained after each surgeon completes the 10 training recordings. Higher scores indicate greater fidelity to the Better Conversations framework, competence is 6 or higher. The performance of surgeons in the automated-training group will be compared with those in the education-specialist training group, and non-inferiority will be evaluated using a 5% non-inferiority margin. Feasibility is defined as greater than or equal to 80 percent of surgeons trained to competence.

    Time frame: At completion of the assessment phase (after 10 training recordings and 5 assessment recordings per surgeon), approximately 3-12 months

Secondary outcomes

  1. Surgeon assessment score

    For each treatment group, the mean and standard deviation of surgeons' assessment scores (range 0-10) will be reported. Higher scores indicate higher competence.

    Time frame: At completion of the assessment phase (after 10 training recordings and 5 assessment recordings per surgeon), approximately 3-12 months

  2. Feeling Heard and Understood

    The mean and standard deviation of Feeling Heard and Understood scores before and after surgeon training will be reported. This patient-survey item uses a 5-point Likert scale (1 = Not at all true to 5 = Completely true), with higher scores indicating better perceived communication. It is used to assess acceptability to patients and preliminary changes associated with surgeon training. For each surgeon, a change score defined as the difference between post-training and pre-training scores will be computed. Surgeon-level change scores will be compared between groups using 95% confidence intervals.

    Time frame: Within 7 days of each patient's surgical consultation; analyzed relative to each surgeon's training completion (pre vs post)

  3. Consumer Assessment of Healthcare Providers and Systems (CAHPS) Surgical Care survey

    CAHPS Surgical Care survey items from 5 patients per surgeon pre-training and 5 patients post-training, aggregated per surgeon and by arm, to characterize patient experience of communication. Items include Yes/No responses (0-1), 3-point responses (0-2), and 4-point responses (0-3). Higher values indicate better experience and scores are expressed as a continuous percent, 0-100. Surgeon-level change scores will be compared between groups using 95% confidence intervals.

    Time frame: Within 7 days of each patient's surgical consultation; analyzed relative to surgeon training completion (pre vs post)

  4. Surgeon Acceptability (Practitioner Opinion Survey)

    Practitioner Opinion Survey administered after training and assessment to evaluate surgeons' perspectives on the training and use of Better Conversations (e.g., usefulness and feasibility). Items use a 0-5 response scale, and higher scores indicate greater acceptability. Summarized overall and by arm. Scores are expressed as a continuous percent, 0-100.

    Time frame: At completion of the assessment phase (after 10 training recordings and 5 assessment recordings per surgeon), approximately 3-12 months

07

Study locations

2 sites
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started Feb 2026 (actual). Primary completion is estimated for Mar 2028, 25 months after the start.

Of 390 non-industry interventional studies with no phase under Communication, half reached primary completion within 18 months of starting (the median), counting those still running; a quarter within 6 and three quarters within 36. This study's planned 25 months is above that.

Counting every sponsor, half of 394 studies reached it within 18 months; a quarter within 6 and three quarters within 36.

How these figures are worked out, and which studies are left out of them.

Registered
Mar 11, 2026
First posted
Mar 16, 2026
StartActual
Feb 27, 2026
Primary completionEst.
Mar 31, 2028
CompletionEst.
Aug 31, 2028
Last update
May 4, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on May 4, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07475104
Collaborators
Wisconsin Partnership Program, Medical College of Wisconsin
Responsible party
Sponsor
First posted
Mar 16, 2026
Start date
Feb 27, 2026
Primary completion
Mar 31, 2028 (estimated)
Completion
Aug 31, 2028 (estimated)
Last update
May 4, 2026

Study contacts

Margaret (Gretchen) L Schwarze, MD, MPP
principal investigator · UW School of Medicine and Public Health

Oversight

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

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