- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04570917
Online Education Intervention to Reduce Ageism Among Undergraduate Students
May 3, 2021 updated by: Nadeeja Wijayatunga, University of Mississippi, Oxford
Effectiveness of an Online Educational Intervention to Reduce Ageism in Undergraduate Students in an Entry-level Nutrition Class
Ageism is common is healthcare workers, and that results in negative outcomes for elderly patients.
This randomized controlled trial is to determine if age bias could be changed by an online learning activity in undergraduate students in an entry-level nutrition class.
Study Overview
Status
Completed
Conditions
Detailed Description
This randomized controlled trial with two parallel arms is to determine the effect of an online educational intervention developed to reduce ageism in undergraduate students enrolled in an entry-level Nutrition class.
Eligible study participants will be randomized into either the "Intervention group" (INT) or the "Control group" (CON).
The two groups will have different learning material delivered online via Blackboard (Learning Management System/LMS).
These include a collection of short videos developed by the researchers, as well as relevant videos available on the web.
Participants in the INT group will learn about aging and ageism, while the CON group will learn about diversity and cultural competence.
Sociodemographic data, percieved risk of COVID-19, preventative behaviors related ot COVID-19 will be collected using a questionnaire at baseline.
Ageism will be assessed using standard questionnaires.
Data collection will be done at three time points: Pre-intervention, immediate post intervention and 2-weeks post-intervention.
Difference between groups for pre-post intervention changes will be assessed.
Study Type
Interventional
Enrollment (Actual)
64
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
-
-
Mississippi
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Oxford, Mississippi, United States, 38677
- University of Mississippi
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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
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- 18 years or older
- Enrolled in 3 sections of the introductory level nutrition course taught by three different instructors.
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: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Intervention group (INT)
An online learning module targeted to reduce ageism will be delivered to the INT group.
|
Participants in this group will go over multiple short videos covering the following content:1).
Myths about aging, 2).
Ageism and its negative effects, 3).
Distorted views about aging among young adults, 4).
Ageism during the COVID-19 pandemic, and 5).
importance of reducing ageism among healthcare professionals.
These will be multiple videos posted on the LMS (Blackboard).
At the end of the lesson, they will be asked to briefly write what they learned on Blackboard as an assignment.
|
|
Active Comparator: Control group (CON)
An online learning module on diversity and cultural competence will be delivered to the CON group.
|
Participants in the control group will go over multiple short videos covering the following content: 1).
Myths about cultural competence, 2) Cultural competence for health care professionals including dietitians, 3).
Connecting culture and food, and 4).
Importance of cultural competence in sports dietitians.
At the end of the lesson, they will be asked to briefly write what they learned.
These will be multiple videos posted on the LMS (Blackboard).
At the end of the lesson, they will be asked to briefly write what they learned on Blackboard as an assignment.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Difference between groups for pre-and post intervention changes in the score of Fraboni's Scale for Ageism
Time Frame: From Pre- to immediate post- intervention
|
Higher Fraboni's score indicates more bias.
|
From Pre- to immediate post- intervention
|
|
Difference between groups for pre- and 2-weeks post intervention changes in the score of Fraboni's Scale for Ageism
Time Frame: From Pre- to 2-weeks post-intervention
|
Higher Fraboni's score indicates more bias.
|
From Pre- to 2-weeks post-intervention
|
|
Difference between groups for pre-post intervention changes in benevolent subscores of the Ambivalent ageism scale
Time Frame: From Pre- to immediate post- intervention
|
Higher benevolent score indicates more benevolent ageism
|
From Pre- to immediate post- intervention
|
|
Difference between groups for pre and 2-weeks post intervention changes in benevolent subscores of the Ambivalent ageism scale Higher score indicates more benevolent bias.
Time Frame: From Pre- to 2-weeks post-intervention
|
Higher benevolent score indicates more benevolent ageism
|
From Pre- to 2-weeks post-intervention
|
|
Difference between groups for pre-post intervention changes in hostile subscores of the Ambivalent ageism scale
Time Frame: From Pre- to immediate post- intervention
|
Higher hostile score indicates more hostile ageism
|
From Pre- to immediate post- intervention
|
|
Difference between groups for pre and 2-week post intervention changes in hostile subscores of the Ambivalent ageism scale
Time Frame: From Pre- to 2-weeks post-intervention
|
Higher hostile score indicates more hostile ageism
|
From Pre- to 2-weeks post-intervention
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Difference between groups for pre-post intervention changes in age-related implicit bias
Time Frame: From Pre- to immediate post- intervention
|
From Pre- to immediate post- intervention
|
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Difference between groups for pre and 2-week post intervention changes in age-related implicit bias
Time Frame: From Pre- to 2-weeks post-intervention
|
From Pre- to 2-weeks post-intervention
|
|
Difference between groups for pre-post intervention changes in the value (years) used to define "old age"
Time Frame: From Pre- to immediate post- intervention
|
From Pre- to immediate post- intervention
|
|
Difference between groups for pre and 2-weeks post intervention changes in the value (years) used to define "old age"
Time Frame: From Pre- to 2-weeks post-intervention
|
From Pre- to 2-weeks post-intervention
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Nadeeja Wijayatunga, PhD, Assistant Professor, Department of Nutrition and Hospitality Management
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)
September 28, 2020
Primary Completion (Actual)
November 11, 2020
Study Completion (Actual)
November 11, 2020
Study Registration Dates
First Submitted
September 25, 2020
First Submitted That Met QC Criteria
September 25, 2020
First Posted (Actual)
September 30, 2020
Study Record Updates
Last Update Posted (Actual)
May 6, 2021
Last Update Submitted That Met QC Criteria
May 3, 2021
Last Verified
November 1, 2020
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 21x-046
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Yes
IPD Plan Description
We will share the de-identified data on ICPSR database
IPD Sharing Time Frame
Within 6 months time after the publication of the primary and secondary analysis planned.
IPD Sharing Access Criteria
Public access database
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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