- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06634433
Training of Trainers Program in IPE for Health Professionals (TTP_IPE)
Training of Trainers Program in Interprofessional Education for Health Professionals
Study Overview
Status
Intervention / Treatment
Detailed Description
Study Design Summary:
This study utilized a quasi-experimental design conducted between June 2023 and March 2024, following the principles of the Declaration of Helsinki. Ethical approval was obtained from the İzmir Democracy University Non-Interventional Ethics Committee (Approval No. 2023/97). The study was supported by TÜBİTAK under program 2237_A with project number 1129B372300447.
Training Program Design and Implementation: The Training of Trainers Program (TTP) in Interprofessional Education (IPE) was developed based on a literature review and the ADDIE instructional design model. The program spanned 40 hours, including 24 hours of synchronous online learning and 16 hours of face-to-face applied sessions. Facilitators from various universities and professions (including doctors, nurses, and other health professionals) led the training.
The first phase involved three days of online theoretical education focusing on key topics such as IPE competencies, communication, mentoring, and scenario writing. Interactive methods like surveys, gamification, and active learning platforms were used. The second phase consisted of two days of practical face-to-face training with small group work and scenario-based activities to foster interprofessional collaboration and communication.
Evaluation Methods: Participants were evaluated using a sociodemographic form, multiple-choice questions, and an IPE Competency Assessment Form (IPE-CAF) with 31 items assessing roles, teamwork, communication, leadership, ethics, and patient relationships. A Training Satisfaction Form with 17 items was also used to gather feedback. Quantitative data were analyzed using SPSS software, with statistical tests like the Wilcoxon signed-rank test and Cronbach's alpha for reliability. Qualitative data from open-ended questions were analyzed using descriptive content analysis.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Konak
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İ̇zmi̇r, Konak, Turkey, 350350
- Izmir Democracy University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Health Professionals: People working in the fields of health sciences such as medicine, dentistry, nursing, nutrition and dietetics, physiotherapy and rehabilitation, or working in academic positions in these fields.
- Trainer Experience: People who have taken part in trainings for health professionals or who will provide training.
- Collaborative Education Experience: Trainers who have previously been involved in interprofessional education processes or who plan to work in this field.
- Volunteerism: Participants who volunteered to participate in the training programme and provided the necessary permissions.
- In addition to all criteria, trainers over the age of 18
Exclusion Criteria:
- Non-Health Professionals: Those working or studying outside of medicine or health sciences will not be included in this programme.
- Those who do not meet the Participation Requirements: Those who cannot attend at least 80% of the online theoretical and face-to-face practical trainings of the programme.
- Non-Volunteers: Those who do not volunteer for the programme and individuals under the age of 18 will be excluded.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Training of Trainers (ToT) Program Group
Participants in this group will receive a two-phase Training of Trainers Program (TTP) aimed at improving their skills in interprofessional education.
The first phase includes three days of online theoretical training covering topics such as interprofessional communication, teamwork, and scenario-based learning.
The second phase consists of two days of face-to-face practical sessions, where participants will engage in scenario-based group work and role-playing activities to reinforce skills in collaborative healthcare practices.
To evaluate the effectiveness of the training program, all participants will complete a pre-test before the training and a post-test after the training
|
The intervention consists of a two-phase Training of Trainers Program (TTP) designed for health professionals aimed at enhancing interprofessional education (IPE) skills.
Phase 1 includes three days of online theoretical training, focusing on topics such as interprofessional collaboration, communication, and conflict resolution.
Phase 2 involves two days of face-to-face practical sessions, where participants engage in scenario-based learning and small group discussions to apply IPE concepts.
The effectiveness of the program is assessed through pre-test and post-test evaluations, measuring changes in participants' knowledge, attitudes, and competencies in interprofessional education.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Improvement in Interprofessional Education Competencies
Time Frame: Pre-test conducted before the intervention and post-test conducted immediately after the completion of the intervention. (20-24 February))
|
The primary outcome measure is the improvement in participants' competencies in interprofessional education (IPE), as assessed through pre- and post-training evaluations.
Competencies include roles and responsibilities, team and teamwork, interprofessional communication, collaborative leadership, relationships with patients, recognizing patient needs, lifelong learning, and ethics.
This will be measured using the IPE Competency Assessment Form (IPE-CAF), which is based on a Likert scale.
Scores will be compared before and after the Training of Trainers Program to assess the effectiveness of the intervention.
|
Pre-test conducted before the intervention and post-test conducted immediately after the completion of the intervention. (20-24 February))
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Training Program Satisfaction
Time Frame: Immediately after the completion of the TTP.
|
Participants' overall satisfaction with the training program will be evaluated using the Training Satisfaction Form.
This form collects feedback on areas such as the enrollment process, training content, trainer effectiveness, and overall program satisfaction.
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Immediately after the completion of the TTP.
|
Collaborators and Investigators
Sponsor
Investigators
- Study Director: Aysel Baser, Asist. Prof., Izmir Democracy University
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimated)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 2023/97
- 1129B372300447 (Other Grant/Funding Number: The Scientific and Technological Research Council of Turkey)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
IPD Sharing Time Frame
IPD Sharing Access Criteria
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- SAP
- ICF
- ANALYTIC_CODE
- CSR
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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