DietCoach: Development and Dietitian Evaluation of a Digital Dietary Counseling Platform (DietCoach)

September 20, 2024 updated by: Wu Jing, University of St.Gallen

The DietCoach study aims to investigate the requirements of a digital dietary counseling platform, and evaluate the dietitian acceptance and usability of the DietCoach platform, which was developed based on the collected requirements. Additionally, the study examines how different levels of patient food purchase data availability affect these factors. The DietCoach platform automatically tracks historic and up-to-date patient food purchase data on loyalty cards and provides nutritional analysis, assisting dietitians in the dietary counseling process. The key research questions (RQ) are:

  1. What are the requirements of a digital dietary counseling system based on food purchase data?
  2. What is acceptance and usability of the DietCoach platform evaluated by dietitians?
  3. How does the availability of patient food purchase data influence the acceptance and perceived usability of the DietCoach platform by dietitians?

Dietitians from several cantonal hospitals in the German-speaking area of Switzerland are invited to participate in the study. To answer RQ1, we conduct a workshop and a survey with dietitians to derive key requirements on dietary counseling systems. To answer RQ2 and RQ3, we use a cross-sectional, mixed-methods, between-subjects study design.

Researchers will evaluate and compare the acceptance and usability of DietCoach in 3 different conditions (3 patients that had different, i.e., high, medium and low, food purchase data availability). Each participant is assigned to the data of one patient. Participants are required to:

  1. use the DietCoach platform to provide at least one dietary recommendation to patient food purchase data in two separate sessions.
  2. provide quantitative and qualitative feedback about the acceptance and usability of the DietCoach platform.

Study Overview

Status

Recruiting

Intervention / Treatment

Detailed Description

The DietCoach study aims to investigate the requirements of a digital dietary counseling platform, and evaluate the dietitian acceptance and usability of the DietCoach platform, which was developed based on the collected requirements. Additionally, the study examines how different levels of patient food purchase data availability affect these factors. The DietCoach platform automatically tracks historic and up-to-date patient food purchases on loyalty cards and provides nutritional analysis.

Dietitians from several cantonal hospitals in the German-speaking area of Switzerland are invited to participate. To collect the key requirements of a digital dietary counseling platform based on food purchase data, we conduct a workshop and a survey, using guiding questions designed based on our research over the last years. To understand the acceptance and usability of DietCoach and how food purchase data availability influences these factors, we use a cross-sectional, mixed-methods, between-subjects study design. Each participant is assigned to the data of one patient. Participants need to:

  1. use the DietCoach platform to provide at least one dietary recommendation to patient food purchase data in two separate sessions.
  2. provide quantitative and qualitative feedback about the acceptance and usability of the DietCoach platform.

The DietCoach usability study includes three conditions (data from three patients), defined by High, Medium, and Low levels of patient food purchase data availability. Data availability is determined by the number of baskets/items (from the major Swiss retail chain) per person in a patient household. Participants are randomly assigned to the data of one patient.

In both the initial and follow-up sessions, participants need to provide at least one dietary recommendation based on the patient's health status and food purchase data over 8 weeks. The food purchase data in the follow-up session covers the 8 weeks immediately following those considered in the initial session. After completing the assigned tasks on the platform, participants are asked to complete a survey assessing their acceptance of and the usability of the DietCoach platform.

Study Type

Observational

Enrollment (Estimated)

30

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Study Locations

    • St.Gallen
      • Saint Gallen, St.Gallen, Switzerland, 9000
        • Recruiting
        • University of St.Gallen
        • Contact:

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

The study aims to include all dietitians in Switzerland as potential participants. However, since recruitment will be conducted through contacting the nutritional departments of cantonal hospitals in the German-speaking area, the participant pool is expected to consist primarily of dietitians from several cantonal hospitals located in the German-speaking region of Switzerland.

Description

Inclusion Criteria:

  • Dietitians in Switzerland
  • German-speaking (the platform is in German, a main language in Switzerland)

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Low patient food shopping coverage
In this group, participants need to give at least one dietary recommendation to a patient whose loyalty card(s) cover(s) a low percentage of food purchases.
Participants are invited to give at least one dietary recommendation to a patient's food purchase data using the DietCoach platform.
Medium patient food shopping coverage
In this group, participants need to give at least one dietary recommendation to a patient whose loyalty card(s) cover(s) a medium percentage of their food purchases.
Participants are invited to give at least one dietary recommendation to a patient's food purchase data using the DietCoach platform.
High patient food shopping coverage
In this group, participants need to give to at least one dietary recommendation to a patient whose loyalty card(s) cover(s) a high percentage of food purchases.
Participants are invited to give at least one dietary recommendation to a patient's food purchase data using the DietCoach platform.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Key requirements of a digital dietary counseling system based on food purchase data
Time Frame: Immediately after the DietCoach intervention

The key requirements for a digital dietary counseling system based on food purchase data will be identified through the dietitian workshop and the dietitian survey. They primarily focus on:

  1. food purchase data availability: number of baskets/items per person in a patient household, and the duration of data availability.
  2. use cases: percentage of participants identifying critical use cases (e.g., recommending alternative food products).
  3. product information: most important product information (e.g., energy, sugar) identified by dietitians for a dietary counseling system.

All outcomes will be quantified using a 5-point Likert scale (from 1 very low importance to 5 very high importance), according to participant responses. Participants are additionally allowed to add more suggestions/recommendation/comments using free text.

Immediately after the DietCoach intervention
Acceptance of the DietCoach platform
Time Frame: Immediately after the DietCoach intervention

Evaluated by the modified Unified Theory of Acceptance and Use of Technology (UTAUT2) constructs. The constructs include performance expectancy, effort expectancy, facilitating conditions, hedonic motivation and behavioral intention.

The construct levels can be indicated by the average score on a 7-point Likert scale.

Immediately after the DietCoach intervention
Usability of the DietCoach platform
Time Frame: Immediately after the DietCoach intervention
Measured by the average System Usability Scale (SUS) score, ranging from 0 to 100. The higher the SUS score, the better the usability
Immediately after the DietCoach intervention

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Jing Wu, M.Sc., University of St.Gallen

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

August 29, 2024

Primary Completion (Estimated)

December 30, 2024

Study Completion (Estimated)

December 30, 2024

Study Registration Dates

First Submitted

September 9, 2024

First Submitted That Met QC Criteria

September 20, 2024

First Posted (Actual)

September 25, 2024

Study Record Updates

Last Update Posted (Actual)

September 25, 2024

Last Update Submitted That Met QC Criteria

September 20, 2024

Last Verified

September 1, 2024

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

We plan to publish anonymized partial food purchase data of the selected patients, and the corresponding dietary recommendations from the DietCoach study participants (dietitians)

  1. The data will be published in an anonymized form.
  2. Only purchase records that can be identified by our food composition database and belong to relevant food categories will be published.

IPD Sharing Time Frame

The data will become available in 2024/2025, published as supplementary materials to the corresponding paper to ensure the result reproducibility. It will be available until participants request to delete their data. Published aggregated results could not be withdrawn retrospectively.

IPD Sharing Supporting Information Type

  • SAP

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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