- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06139471
Efficacy of a Virtual Reality-Enhanced Gagne's Instructional Model (VR-gagne)
November 17, 2023 updated by: Alexandria University
Exploring the Efficacy of a Virtual Reality-Enhanced Gagne's Instructional Model in Promoting Nursing Students' Aging Rejection and Willingness Towards Gerontological Care
Gagne's conditions of instructional learning theory, it presumed that several learning levels was exist that require different instruction types, and external and internal environments, commonly referred to as "conditions of learning".
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
According to Robert Gagne's conditions of instructional learning theory, it presumed that several learning levels was exist that require different instruction types, and external and internal environments, commonly referred to as "conditions of learning", for every learning type.
These internal conditions related to the learner's preexisting knowledge and external ones related to the instructions and teaching strategies provided by the instructor.
The theory emphasizes the importance of both internal and external factors in creating a conducive learning environment that fosters effective learning outcomes According to this theorist, there are five primary knowledge categories, including verbal information, cognitive strategies, attitudes, and motor and intellectual skills.
Study Type
Interventional
Enrollment (Actual)
100
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
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Alexandria, Egypt
- Faculty of nursing
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Please Select A Country
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Alexandria, Please Select A Country, Egypt, 21913
- Mohamed Husien
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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
- Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Agreement to participate in this study.
- Have a Microsoft team's account and able to use it.
- No previous participation in any gerontological educational course either compulsory or elective.
exclusion Criteria: previous participation in any gerontological educational course either compulsory or elective.
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 |
|---|---|
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Experimental: study group (VR-enhanced Gagne's Instructional Model)
receive VR-enhanced Gagne's Instructional Model
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Virtual Reality-Enhanced Gagne's Instructional Model
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No Intervention: STUDY group
doesn't VR-enhanced Gagne's Instructional Model
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Willingness to Work with Elderly People Scale (WEPS)
Time Frame: three months
|
Nursing students who exposed to the VR-enhanced Gagne's Instructional Model will exhibit higher score in Willingness to Work with Elderly People Scale (WEPS) than who don't exposed to such therapy.
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three months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The Fraboni Scale of Ageism (FSA)
Time Frame: 3 months
|
Nursing students who exposed to the VR-enhanced Gagne's Instructional Model will exhibit lower score in The Fraboni Scale of Ageism (FSA) than who don't exposed to such therapy.
|
3 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: mohamed H atta, Faculty of nursing, Alexandria university, Egypt
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 (Actual)
April 30, 2023
Study Completion (Actual)
June 30, 2023
Study Registration Dates
First Submitted
November 2, 2023
First Submitted That Met QC Criteria
November 17, 2023
First Posted (Estimated)
November 20, 2023
Study Record Updates
Last Update Posted (Estimated)
November 20, 2023
Last Update Submitted That Met QC Criteria
November 17, 2023
Last Verified
November 1, 2023
More Information
Terms related to this study
Other Study ID Numbers
- 13-6-2021
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.