- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06560567
Attitudes and Barriers of Prosthetics and Orthotics Professionals in Turkey Towards 3D Printers and Technology
Investigation of the Attitudes and Barriers of Prosthetics and Orthotics Professionals in Turkey Towards 3D Printers and Technology
Study Overview
Status
Conditions
Detailed Description
It is known that there are generally concerns about high capital costs and return on investment in the use of 3D printer technology in Turkey.
It is known that there is no study in Turkey to investigate the attitudes and barriers of prosthetics and orthotics professionals towards 3D printers and technology. Therefore, the attitudes and barriers of prosthetics and orthotics professionals towards 3D printers and technology will be questioned in the study. It was aimed to reveal the perspectives and concerns about 3D printers and technology and to emphasize the importance of increasing the number of education and competent personnel regarding the dissemination of technological applications in practice.
In the study investigating the attitudes and barriers of prosthetics and orthosis professionals towards 3D printers and technology in Turkey, a total of 131 participants, 29 female and 102 male, aged at least 18 and at most 65 years old, were included.
The participants first filled out the Demographic Information Form. This form includes demographic information such as the participant's age, gender, education level, profession, duration of professional experience, geographical region where they work, the number of in-service trainings they receive in the field of orthosis and prosthesis, weekly working hours and the number of daily patients they communicate with.
At the end of the demographic information, the participants were asked to state open-endedly what they had concerns about technology that they could not define.
In addition, questions created according to the Technology Acceptance Model (TAM) and the Affinity for Technology Interaction (ATI) were also answered by the participants.
When the participants were asked whether they had concerns about 3D printers and technology that they could not define, it was determined that they mostly answered no. When the participants who had concerns were asked open-endedly about their concerns, the answers given were mostly about the lack of information or competent personnel for use when the answers were collected under common headings. It was observed that the technology acceptance model and proximity to technology had an effect on the time spent in the profession and the total score of ATI.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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İstanbul
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Bakırköy, İstanbul, Turkey, 34158
- Ayşe Yazgan
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- As working in an Orthosis and Prosthesis Application Center
- Being 18 years of age or older.
Exclusion Criteria:
- Insufficient cognitive level to answer the survey
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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Prosthetics and Orthotics Professionals
A total of 131 participants, 29 female and 102 male, aged at least 18 and at most 65 years old, completed the survey.
The inclusion criteria for the participants were determined as working in an Orthosis and Prosthesis Application Center and being 18 years of age or older.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Technology Acceptance Model (TAM)
Time Frame: immediately after screening
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While creating the TAM survey, a total of 23 questions were asked to measure the perceived of usefulness, perceived ease of use, attitude variable, intention variable and the behavior variable towards 3D Printing and Technology. Questions were also asked to determine demographic characteristics. Demographic information questions are; participant's age, gender, education level, job, work experience (years), job geographic region, number of in-service trainings in orthotics and prosthetics, weekly working hours and number of patients contacted daily. At the end of the demographic information, participants were asked to clearly state their concerns about technology that they could not define. While the questions regarding demographic targets in the survey were categorical, the questions measuring perceptions regarding the use of 3D printing and technology included 5-point Likert type answers. (1: Strongly disagree, 2: Disagree, 3: Neutral, 4: Agree, 5: Strongly agree) |
immediately after screening
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Affinity for Technology Interaction (ATI)
Time Frame: immediately after screening
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ATI evaluates the affinity to technology by focusing on user-system interaction.
The scale takes into account cognitive needs to base affinity to technology on basic psychological structures and the questions are formulated accordingly.
The title of the scale includes the statement that questions will be asked about interaction with technical systems.
In our study, 3D Printer technology was stated to the participants as a technical system.
The scale consists of 9 questions and the answers are in the form of a 6-point Likert scale: '1=Totally disagree, 2=Mostly disagree, 3=Partially disagree, 4=Partially agree, 5=Mostly agree, 6=Totally agree'.
Finally, an average score was calculated over the 9 questions.
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immediately after screening
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Ayşe Yazgan, https://www.medipol.edu.tr/
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 (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- MedipolU-OP-AY-02
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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