Evaluation of Nutrition Training Augmented With Digital Technology in Graduate Medical Education

Sponsor
University of Texas at Austin (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT06088251
Collaborator
(none)
88
2
2.2

Study Details

Study Description

Brief Summary

We will conduct a randomized controlled evaluation of standard nutrition education vs. standard education + Nutri, and interactive clinical software that automates diet assessment and guides resident physicians through personalized and evidence-based diet counseling. We will evaluate differences in resident-reported diet counseling competence and self-efficacy using survey measures. We will evaluate skills using a simulated patient appointment and coding scheme described in prior work.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Nutri Training
  • Behavioral: Standard Nutrition Education
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
88 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Health Services Research
Official Title:
Evaluation of Nutrition Training Augmented With Digital Technology in Graduate Medical Education
Anticipated Study Start Date :
Oct 24, 2023
Anticipated Primary Completion Date :
Dec 31, 2023
Anticipated Study Completion Date :
Dec 31, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Nutri Training

Nutri Training will begin with 1) a presentation of diet counseling evidence and best practices for advising patients, along with information about nutrition recommendations for patients with chronic illness and 2) tools supporting the patient for follow-up. This content will be delivered via a live demonstration of the Nutri interactive software and case demonstration, a novel approach to delivering the learning objectives of standard nutrition education for residents.

Behavioral: Nutri Training
Nutri Training will begin with 1) a presentation of diet counseling evidence and best practices for advising patients, along with information about nutrition recommendations for patients with chronic illness and 2) tools supporting the patient for follow-up. This content will be delivered via a live demonstration of the Nutri interactive software and case demonstration, a novel approach to delivering the learning objectives of standard nutrition education for residents.

Active Comparator: Standard Nutrition Education

Standard Nutrition Training will present an overview of 1) nutrition recommendations for patients with chronic disease and 2) cover the role of a registered dietitian and referrals.

Behavioral: Standard Nutrition Education
Standard Nutrition Education Standard Nutrition Training will present an overview of 1) nutrition recommendations for patients with chronic disease and 2) cover the role of a registered dietitian and referrals.

Outcome Measures

Primary Outcome Measures

  1. Diet Counseling Competence [Resident pre-assessment and post-assessment, expected to be 2 weeks after enrollment]

    Self-report of diet counseling competency; 4-point Likert-like scale scale; higher score means better outcome

  2. Diet Counseling Self-Efficacy [Resident pre-assessment and post-assessment, expected to be 2 weeks after enrollment]

    Self-report of confidence (self-efficacy) in diet counseling; 4-point Likert-like scale scale; higher score means a better outcome.

  3. Diet Counseling Skills [Post-hoc analysis of simulation activity, expected to be at 2 weeks after training intervention]

    We will also use an observation checklist to systematically capture resident shared decision-making and diet counseling skills. We will create this checklist based on a literature review of similar tools, such as the Shared Decision Making (SDM) SDM-9 and the coding scheme described in Alexander 2011.

Other Outcome Measures

  1. Physician Diet Counseling Outcome Expectations [Resident pre-assessment and post-assessment, expected to be 2 weeks after enrollment]

    Self-report of diet counseling outcome expectations; 5-point Likert-like scale; higher score means better outcome.

  2. Semi-structured debrief interview [Post-hoc analysis of simulation activity, expected to be at 2 weeks after training intervention]

    Semi-structured debrief interview to better understand the resident's experience and feedback on the training session and simulation activity.

  3. Training Satisfaction [Resident post-assessment, expected to be 2 weeks after enrollment]

    Self-report of satisfaction with training; 5-point Likert-like scale scale; higher score means a better outcome.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 65 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Dell Medical School Internal Medicine Residents

  • Dell Medical School Family Medicine Residents

Exclusion Criteria:
  • N/A

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • University of Texas at Austin

Investigators

  • Principal Investigator: Marissa Burgermaster, PhD, University of Texas at Austin

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
University of Texas at Austin
ClinicalTrials.gov Identifier:
NCT06088251
Other Study ID Numbers:
  • 00005155
First Posted:
Oct 18, 2023
Last Update Posted:
Oct 18, 2023
Last Verified:
Oct 1, 2023
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by University of Texas at Austin
Additional relevant MeSH terms:

Study Results

No Results Posted as of Oct 18, 2023