Online Education Intervention to Reduce Ageism Among Undergraduate Students

Sponsor
University of Mississippi, Oxford (Other)
Overall Status
Completed
CT.gov ID
NCT04570917
Collaborator
(none)
64
1
2
1.4
44.3

Study Details

Study Description

Brief Summary

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.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Online educational intervention to reduce ageism
  • Behavioral: Online educational intervention to enhance cultural competance
N/A

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 Design

Study Type:
Interventional
Actual Enrollment :
64 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Participant)
Primary Purpose:
Supportive Care
Official Title:
Effectiveness of an Online Educational Intervention to Reduce Ageism in Undergraduate Students in an Entry-level Nutrition Class
Actual Study Start Date :
Sep 28, 2020
Actual Primary Completion Date :
Nov 11, 2020
Actual Study Completion Date :
Nov 11, 2020

Arms and Interventions

Arm Intervention/Treatment
Experimental: Intervention group (INT)

An online learning module targeted to reduce ageism will be delivered to the INT group.

Behavioral: Online educational intervention to reduce ageism
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.

Behavioral: Online educational intervention to enhance cultural competance
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.

Outcome Measures

Primary Outcome Measures

  1. Difference between groups for pre-and post intervention changes in the score of Fraboni's Scale for Ageism [From Pre- to immediate post- intervention]

    Higher Fraboni's score indicates more bias.

  2. Difference between groups for pre- and 2-weeks post intervention changes in the score of Fraboni's Scale for Ageism [From Pre- to 2-weeks post-intervention]

    Higher Fraboni's score indicates more bias.

  3. Difference between groups for pre-post intervention changes in benevolent subscores of the Ambivalent ageism scale [From Pre- to immediate post- intervention]

    Higher benevolent score indicates more benevolent ageism

  4. 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. [From Pre- to 2-weeks post-intervention]

    Higher benevolent score indicates more benevolent ageism

  5. Difference between groups for pre-post intervention changes in hostile subscores of the Ambivalent ageism scale [From Pre- to immediate post- intervention]

    Higher hostile score indicates more hostile ageism

  6. Difference between groups for pre and 2-week post intervention changes in hostile subscores of the Ambivalent ageism scale [From Pre- to 2-weeks post-intervention]

    Higher hostile score indicates more hostile ageism

Secondary Outcome Measures

  1. Difference between groups for pre-post intervention changes in age-related implicit bias [From Pre- to immediate post- intervention]

  2. Difference between groups for pre and 2-week post intervention changes in age-related implicit bias [From Pre- to 2-weeks post-intervention]

  3. Difference between groups for pre-post intervention changes in the value (years) used to define "old age" [From Pre- to immediate post- intervention]

  4. Difference between groups for pre and 2-weeks post intervention changes in the value (years) used to define "old age" [From Pre- to 2-weeks post-intervention]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • 18 years or older

  • Enrolled in 3 sections of the introductory level nutrition course taught by three different instructors.

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of Mississippi Oxford Mississippi United States 38677

Sponsors and Collaborators

  • University of Mississippi, Oxford

Investigators

  • Principal Investigator: Nadeeja Wijayatunga, PhD, Assistant Professor, Department of Nutrition and Hospitality Management

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Nadeeja Wijayatunga, Assistant Professor, University of Mississippi, Oxford
ClinicalTrials.gov Identifier:
NCT04570917
Other Study ID Numbers:
  • 21x-046
First Posted:
Sep 30, 2020
Last Update Posted:
May 6, 2021
Last Verified:
Nov 1, 2020
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Nadeeja Wijayatunga, Assistant Professor, University of Mississippi, Oxford

Study Results

No Results Posted as of May 6, 2021