Learning Diagnostic Skills Online (German: Diagnostik Skills Online Lernen) (DiSkO)

March 15, 2022 updated by: Ruth von Brachel, Ruhr University of Bochum

Clinical psychologists give diagnoses to their patients everyday and these diagnoses determine if and how these patients will be treated. Misdiagnoses can have severely adverse effects. Therefore, teaching diagnostic skills to clinical psychologists is very important during their undergraduate, graduate and postgraduate training.

One major problem in teaching diagnostics is that there are too few opportunities to practice with real patients due to legal and ethical restrictions. The aim of the DiSkO-project is, therefore, the development and evaluation of a blended learning course to teach diagnostic skills to (future) clinical psychologists.

In order to make the diagnostic training more practical a series of video files of simulated diagnostic interviews will be presented in an online course. These video files will be divided in different segments and presented with questions and automatic feedback. In a second step, learners will make a transfer to a real face-to-face diagnostic situation with an actor simulating a patient.

The DiSkO- course will be evaluated in a randomized-controlled trial at three universities in Germany (Ruhr-University of Bochum, Philipps University of Marburg, University of Cologne). To test whether students are equally good in administering a diagnostic interview after taking the DiSkO-course compared to students who took part in a traditional face-to-face university course a noninferiority-analysis will be conducted. Furthermore, diagnostic knowledge and attitudes toward evidence-based assessment after taking part in DiSkO vs. the face-to-face course will be compared.

The investigators aim at disseminating the open source DiSkO-course to other universities or institutions of tertiary education in Germany with the aim of improving the diagnostic training for students, better prepare them for their clinical practice and thus improve patients' health care in Germany.

Study Overview

Study Type

Interventional

Enrollment (Actual)

350

Phase

  • Not Applicable

Contacts and Locations

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

Study Locations

    • Hesse
      • Marburg, Hesse, Germany, 35032
        • Philipps University of Marburg
    • North Rhine-westphalia
      • Bochum, North Rhine-westphalia, Germany, 44787
        • Ruhr-University Bochum
      • Cologne, North Rhine-westphalia, Germany, 50969
        • University of Cologne

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

16 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Psychology bachelor students of a cooperating university (Ruhr-University of Bochum, University of Cologne, Philipps-University of Marburg)

Exclusion Criteria:

  • previous participation in a diagnostic seminar

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

  • Primary Purpose: Other
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: intervention group
blended learning
The blended learning course consists of two parts. The first part is an online course with case studies and instructional videos providing basic clinical diagnostic knowledge and the ability to conduct structured clinical interviews. In the second part, learners get to discuss the course content with a teacher, practice their interviewing skills with other students and make a transfer to a real face-to-face diagnostic situation with an actor simulating a patient.
Active Comparator: control group
Teaching format as usual
The teaching format as usual represents the usual teaching of clinical diagnostic knowledge and the ability to conduct structured clinical interviews. Also in this intervention students also have the opportunity to discuss the course content with a teacher, practice their interviewing skills with other students and conduct a structured interview with an actor simulating a patient.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Behavioral Measure: Performance in a structured interview
Time Frame: 13 weeks
Conducting a 15 minute section of a structured interview with a patient played by an actor. This interview is videotaped and then rated by independent evaluators regarding e.g. rules of correct implementation and clincial interviewing skills.
13 weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Knowledge Test A
Time Frame: 1 week
A test of basic clinical diagnostic knowledge developed and previously piloted by the study authors. Using the data from the piloting, two parallel 15-Item versions (A and B) were created, which students answered before and after the intervention.
1 week
Knowledge Test B
Time Frame: 14 weeks
A test of basic clinical diagnostic knowledge developed and previously piloted by the study authors. Using the data from the piloting, two parallel 15-Item versions (A and B) were created, which students answered before and after the intervention.
14 weeks
Münster Questionnaire for the Evaluation of Seminars - revised (MFE-Sr; Thielsch & Hirschfeld, 2010)
Time Frame: 14 weeks

7-point Likert scale (min.: 1, max.:7)

The following 6 Items from the MFE-Sr were used:

Item Number 14: "The content of this course was too difficult for me." Item Number 15: "The pace of teaching was too fast for me." Item Number 16: "The time commitment associated with the course overwhelmed me." Item Number 25: "I learned a lot in this course." Item Number 26: "I would recommend this course to other students."

Item 14-16: higher values indicate worse outcome, Item 25-26: higher values indicate better outcome

14 weeks
Website-Clarity, Likeability, Informativeness, and Credibility (Web-CLIC; Thielsch & Hirschfeld, 2019)
Time Frame: 14 weeks

A 12-item questionnaire measuring a users' subjective view on web content, regarding its clarity, likeability, informativeness and credibility. The whole 12-item scale and one additionally created item regarding the credibility ("I completely trusted the content in DiSkO") were used.

7-point Likert scale (min.: 1, max.:7) higher values indicate better outcome

14 weeks
Brief scale for teaching evaluation (Zumbach, Spinath, Schahn, Friedrich & Kögel, 2007)
Time Frame: 14 weeks

The following 3 Items were used:

Item Number 1: "The subject matter was appropriately illustrated (e.g. by examples, visualizations, etc.)." Item Number 2: "The course was clearly structured." Item Number 3: "The learning objectives of the course were clearly defined."

7-point Likert scale (min.: 1, max.:7) higher values indicate better outcome

14 weeks
Usability Metric for User Experience - Lite (UMUX-Lite; Lewis et al., 2013)
Time Frame: 14 weeks

A 2-item scale assessing perceived usability.

7-point Likert scale (min.: 1, max.:7) higher values indicate better outcome

14 weeks
Visual Aesthetics of Websites Inventory - Short (VisAWI-S; Moshagen & Thielsch, 2013)
Time Frame: 14 weeks

A 4-item scale measuring subjectively perceived aesthetics. The 4-item scale and one additionally created item ("DiSkO is designed to be visually appealing") were used.

7-point Likert scale (min.: 1, max.:7) higher values indicate better outcome

14 weeks
Overall impression
Time Frame: 14 weeks

One item using the german school grading system ranging from 1 (very good) to 6 (unsatisfactory):

"Overall: I give the course an overall grade of ..."

14 weeks
Acceptance of structured interviews questionnaire (Bruchmüller et al., 2011)
Time Frame: 14 weeks

A 11-item questionnaire measuring the estimated patient satisfaction with structured interviews.

Item 1:

visual analogue scale (0-100) higher values indicate better outcome

Item 2-11:

4-point Likert scale (min.: 0, max.:3)

Item 2,3,4,5 and 8 higher values indicate worse outcome Item 6,7,9,10 and 11 higher values indicate better outcome

14 weeks

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Lesson evaluation
Time Frame: After each lesson during the intervention (during week 8-10)

Each lesson (1-8) of the online part of the blended learning course was evaluated using the following questions:

"How much time (in minutes) did you spend working on this lesson?" "How concentrated did you work on the content of this lesson?" "I give this lesson an overall grade ..." "Here is space for your feedback on this lesson (e.g. criticism, suggestions, proposals for improvement)"

After each lesson during the intervention (during week 8-10)

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Ruth E von Brachel, Dr., Ruhr-University Bochum

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)

April 12, 2021

Primary Completion (Actual)

February 14, 2022

Study Completion (Actual)

February 14, 2022

Study Registration Dates

First Submitted

January 17, 2022

First Submitted That Met QC Criteria

March 15, 2022

First Posted (Actual)

March 24, 2022

Study Record Updates

Last Update Posted (Actual)

March 24, 2022

Last Update Submitted That Met QC Criteria

March 15, 2022

Last Verified

March 1, 2022

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 16DHB3010

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

Yes

IPD Plan Description

All anonymized IPD will be shared with the exception of demographic data which, due to rare constellations, entail a risk of deanonymization of individual participants. The IPD will be made available via the Internet database Psychdata (https://www.psychdata.de) of the Leibnitz Center for Psychological Information and Documentation.

IPD Sharing Time Frame

The IPD will become available after data analysis (anticipated: September 2022) and will be shared for at least 10 years.

IPD Sharing Access Criteria

In order to access the IPD, users must agree to the Data Recipient Agreement and Terms of Use of the internet database Psychdata (https://www.psychdata.de/index.php?main=take&sub=empfang&lang=eng).

These, among other things, exclude commercial use of the data, protect the interests of the data providers, and ensure the anonymity of the individuals studied.

IPD Sharing Supporting Information Type

  • Statistical Analysis Plan (SAP)
  • Analytic Code

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

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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