- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05695326
Effects of a 3D Printing Technology Learning Program
February 21, 2023 updated by: Ken Kondo, Gunma PAZ College
Effects of a 3D Printing Technology Learning Program for Rehabilitation Professionals: a Randomized Control Trial
3D printing technology helps rehabilitation professionals make an order-made assistive device (AD).
However, most have not learned how to use the technology for clinical practice.
The study is aimed to evaluate a 3D printing technology learning program for rehabilitation professionals.
Eligible participants who have a licence for physical, occupational or speech-language therapy and have not experienced learning any 3D printing technology.
The learning program was conducted in accordance with Kolb's Experiential Learning Theory (Morris TH, 2020).
The program was conducted over eight weeks.
The outcome measure included the Japanese version of the modified Technology Acceptance Model questionnaire (TAM-J).
It consists of 13 items and four scales; Perception of usefulness (28 points total), Perception of ease of use (35 points total), Attitude toward use (14 points total) and Intention to use (14 points total).
Within-group analyses were performed using the Wilcoxon signed-rank test for the TAM-J between different time points.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Anticipated)
10
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 Contact
- Name: Ken Kondo, PhD
- Phone Number: 0273653366
- Email: kenkondoot@gmail.com
Study Locations
-
-
Kanayama
-
Fujisawa, Kanayama, Japan
- Recruiting
- Shonan Keiiku Hospital
-
Contact:
- Sho Maruyama, phD
-
-
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
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Eligible participants who have a licence for physical, occupational or speech-language therapy
Exclusion Criteria:
- Participants who have experienced learning any 3D printing technology.
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: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Effects of a 3D Printing Technology Learning Program
|
The study is aimed to evaluate a 3D printing technology learning program for rehabilitation professionals
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The Japanese version of modified Technology Acceptance Model questionnaire
Time Frame: Change from Baseline a score of the Japanese version of modified Technology Acceptance Model questionnaire at 2 months
|
A higher score means the strong acceptance of 3D printing technology(score range is 13 to 91 points)
|
Change from Baseline a score of the Japanese version of modified Technology Acceptance Model questionnaire at 2 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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)
February 1, 2023
Primary Completion (Anticipated)
March 31, 2023
Study Completion (Anticipated)
March 31, 2023
Study Registration Dates
First Submitted
January 5, 2023
First Submitted That Met QC Criteria
January 12, 2023
First Posted (Actual)
January 25, 2023
Study Record Updates
Last Update Posted (Estimate)
February 23, 2023
Last Update Submitted That Met QC Criteria
February 21, 2023
Last Verified
February 1, 2023
More Information
Terms related to this study
Other Study ID Numbers
- PAZ22-2-1
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
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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