- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06175364
Evidence-Based Orthotics Prosthetics Practices
Investigation of the Views of Health Professionals in the Field of Orthotics Prosthetics on Evidence-Based Orthotics Prosthetics Practices
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Three data collection tools will be used as data collection methods for the research. These data collection tools; demographic information form, Health Sciences Evidence-Based Practice Survey and Information Literacy Self-Efficacy Scale. Surveys will be sent to participants to be filled out via Google Forms.
Inclusion criteria: Having been working in hospitals, clinics, academic units, etc. in Turkey for at least 6 months. Being able to read and write Turkish. Exclusion criteria; Those who graduated in the field of Orthosis and Prosthesis and work in other clinics and units.
The data will be evaluated in the statistical package program IBM Statistical Package for the Social Sciences Statistics 26.0 (IBM Corp, New York, USA).
To determine the sample size in the study, G*Power 3.1.9.4 software was used to calculate the number of people to take part in the study. The effect size of the study was determined as 134 participants with 80% statistical power and 5% significance level. Our research will be conducted between December 2023 and June 2024.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: alican ak
- Phone Number: +905549239227
- Email: alican.ak@outlook.com
Study Locations
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Istanbul, Turkey
- Istanbul Medipol University
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Contact:
- Medipol Universitesi
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Inclusion Criteria: Having been working in hospitals, clinics, academic units, etc. in Turkey for at least 6 months.
- Being able to read and write Turkish
Exclusion Criteria:
- Those who graduated in the field of Orthosis and Prosthesis and work in other clinics and units
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Other: Health Professionals in the Field of Orthotics Prosthetics
Health professionals in the field of orthotics and prosthetics generally include orthotic and prosthetic specialists, physiotherapists, rehabilitation specialists, orthopedic surgeons, biomechanics experts, physiologists, and engineers.
These professionals specialize in the design, production, application, and rehabilitation of orthoses and prostheses.
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Three data collection tools will be used as data collection methods for the research.
These data collection tools; demographic information form, Health Sciences Evidence-Based Practice Survey and Information Literacy Self-Efficacy Scale.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Health Sciences Evidence-Based Practice Survey
Time Frame: 2 weeks
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It is a form created to collect participants' information about evidence-based practices in health sciences.
The survey is a 10-point Likert scale with a total of 60 items.
Main; The scale consists of 3 subheadings: belief-attitude (12 items with total scores ranging from 12 to 120), practice (36 items with total scores ranging from 36 to 360) and barriers-facilitators (12 items with scores ranging from 12 to 120).
A higher score indicates a more supportive attitude or behavior towards the implementation of evidence-based practices in clinical practice.
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2 weeks
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Collaborators and Investigators
Sponsor
Investigators
- Study Director: Gizem BOZTAŞ ELVERİŞLİ, Dr.Öğr.Üye., MedipolIU
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- IMU-OP-AA-01
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
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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