RCT Regarding SDM Online Training and Face-to-face SDM Training

June 7, 2019 updated by: Dr. Kathrin Gschwendtner, University Hospital Heidelberg

Randomized Controlled Trial Regarding (RCT) Innovative Dissemination Strategies for a Brief Shared Decision Making (SDM) Intervention for Oncologists: Web-based SDM Online Training and Individualized, Context-based Face-to-face SDM Training

Cancer patients often report that they are not included in important treatment decisions. Numerous studies have shown that a training concerning Shared Decision Making (SDM) for physicians can improve this situation. This does not only lead to a better quality of the doctor-patient interaction, but may have a positive long term impact on treatment adherence, the psychological well-being and the coping abilities of the patients. However, previous experience regarding the implementation of SDM training programs show that it is difficult to recruit physicians for an external SDM group training due to the extensive workload of the physicians. In light of the available evidence on the effectiveness of SDM training and the low motivation by oncologists for traditional SDM group training, this study aims to develop and evaluate a brief SDM intervention. This intervention is disseminated in two different ways which both might be attractive for oncologists. On the one hand an individual face-to-face context-based SDM training is designed and conducted by a trainer at the workplace of the participating oncologists. On the other hand a web-based SDM online training is developed. Both SDM interventions are developed on the basis of an SDM manual evaluated in previous studies.

This study therefore aims to examine the effectiveness of different disseminations strategies (individualized face-to-face context-based SDM individual training vs. web-based SDM online training) compared to a control group without any training. It will be analyzed which improvements in medical SDM competence can be accomplished by the different SDM trainings. Further the effects of the training on SDM knowledge, quality of the doctor-patient interaction and SDM self-efficacy expectation will be evaluated.

Study Overview

Status

Completed

Intervention / Treatment

Study Type

Interventional

Enrollment (Actual)

161

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

      • Hamburg, Germany, 20246
        • University Hospital Hamburg-Eppendorf
    • Baden-Wuerttemberg
      • Heidelberg, Baden-Wuerttemberg, Germany, 69115
        • University Hospital Heidelberg

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

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  1. Oncologists or physicians treating a significant percentage of breast and/or colorectal cancer patients
  2. Internet access

Exclusion Criteria:

  • No Exclusion Criteria

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: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: SDM Online Training
The intervention consists of a SDM training for oncologists, which is conducted in the form of a web-based SDM online Training (intervention group I). During training, the oncologists are guided to use decision aids for breast and colon cancer patients in their consultations, which were developed and evaluated in a previous project. The SDM training has the same duration (one session à 120 minutes) in both intervention groups. Doctors in the intervention group receive decision aids for breast cancer and colorectal cancer patients during training. The training contents are based on an already developed, evaluated and published SDM manual. The SDM online training works on the modeling principle.
Active Comparator: Face-to-Face SDM Training
The intervention consists of a SDM training for oncologists, which is conducted in the form of an individualized, context-based SDM individual face-to-face training at the workplace of the participants (intervention group II). During training, the oncologists are guided to use decision aids for breast and colon cancer patients in their consultations, which were developed and evaluated in a previous project. The SDM training has the same duration (one session à 120 minutes) in both intervention groups. Doctors in the intervention group receive decision aids for breast cancer and colorectal cancer patients during training. The training contents are based on an already developed, evaluated and published SDM manual. The individual training works on the coaching principle.
No Intervention: Control Group
The Control Group receives no SDM Training. All participants of the Control Group will be offered to participate in the SDM Online Training after T2.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change from baseline in SDM competence measured by an objective Rating (OPTION)
Time Frame: T0 (2 weeks before Training) and T1 (1 weeks after Training)
To measure the SDM competence the OPTION scale (Observing Patient Involvement; Elwyn et al., 2003; Elwyn et al., 2005; Goss et al., 2007.) will be used. The OPTION scale is a validated instrument for measuring the process steps of Shared Decision Making. The consultations are assessed on the basis of 12 items. It shows good reliability with a value of 0.79. The Option rating is based on video recordings and anonymised transcripts. A consultation will be assessed by two blinded raters. The average value per item is used as final value. For the consultations standardized patients are deployed.
T0 (2 weeks before Training) and T1 (1 weeks after Training)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change from baseline in SDM competence by subjective standardized patient rating (Dyadic Option)
Time Frame: T0 (2 weeks before Training), T1 (1 weeks after Training), T2 (3 month after T1)
Dyadic OPTION (Melbourne et al., 2010), patient version
T0 (2 weeks before Training), T1 (1 weeks after Training), T2 (3 month after T1)
Change from baseline in SDM competence by subjective standardized patient rating (Patient Perception Scale)
Time Frame: T0 (2 weeks before Training), T1 (1 weeks after Training), T2 (3 month after T1)
Patient Perception Scale (PPS; Janz et al., 2004)
T0 (2 weeks before Training), T1 (1 weeks after Training), T2 (3 month after T1)
Change from baseline in SDM competence by subjective standardized patient rating (SDM-Q-9)
Time Frame: T0 (2 weeks before Training), T1 (1 weeks after Training), T2 (3 month after T1)
SDM-Q-9 (Kriston et al, 2010; Simon, Loh, & Haerter, 2007)
T0 (2 weeks before Training), T1 (1 weeks after Training), T2 (3 month after T1)
Change from baseline in SDM competence by subjective physician rating (Dyadic Option)
Time Frame: T0 (2 weeks before Training), T1 (1 weeks after Training), T2 (3 month after T1)
Dyadic OPTION (Melbourne et al., 2010), physician version
T0 (2 weeks before Training), T1 (1 weeks after Training), T2 (3 month after T1)
Change from baseline in SDM competence by subjective physician rating (Physician-Perception-Scale)
Time Frame: T0 (2 weeks before Training), T1 (1 weeks after Training), T2 (3 month after T1)
Physician-Perception-Scale (PPS; Janz et al., 2004)
T0 (2 weeks before Training), T1 (1 weeks after Training), T2 (3 month after T1)
Change from baseline in SDM competence by subjective physician rating (SDM-Q-9)
Time Frame: T0 (2 weeks before Training), T1 (1 weeks after Training), T2 (3 month after T1)
SDM-Q-Doc (Scholl et al., 2012)
T0 (2 weeks before Training), T1 (1 weeks after Training), T2 (3 month after T1)
Change from baseline in quality of doctor-patient-interaction by subjective Patient rating (Questionnaire on the Quality of physician-patient interaction)
Time Frame: T0 (2 weeks before Training), T1 (1 weeks after Training), T2 (3 month after T1)
Questionnaire on the Quality of physician-patient interaction (QQPI, Bieber et al., 2010), Patient version
T0 (2 weeks before Training), T1 (1 weeks after Training), T2 (3 month after T1)
Change from baseline in quality of doctor-patient-interaction by subjective Physician rating (Questionnaire on the Quality of physician-patient interaction)
Time Frame: T0 (2 weeks before Training), T1 (1 weeks after Training), T2 (3 month after T1)
Questionnaire on the Quality of physician-patient interaction (QQPI, Bieber et al., 2010), physician version
T0 (2 weeks before Training), T1 (1 weeks after Training), T2 (3 month after T1)

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Christiane Bieber, PD, University Hospital Heidelberg

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Helpful Links

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

May 1, 2016

Primary Completion (Actual)

December 31, 2018

Study Completion (Actual)

January 31, 2019

Study Registration Dates

First Submitted

January 25, 2016

First Submitted That Met QC Criteria

February 1, 2016

First Posted (Estimate)

February 4, 2016

Study Record Updates

Last Update Posted (Actual)

June 11, 2019

Last Update Submitted That Met QC Criteria

June 7, 2019

Last Verified

June 1, 2019

More Information

Terms related to this study

Other Study ID Numbers

  • DKH109956, DKH110010

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

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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