Education Program for Enhancing Healthcare Students' Attitudes Toward People Living With Dementia

Sponsor
Universitas Airlangga (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT06122623
Collaborator
Tokyo University (Other), Kawasaki City College of Nursing (Other)
400
1
8.2

Study Details

Study Description

Brief Summary

The aim of this single-arm pre-post study is to examine the effectiveness of gaming-based dementia educational programs for enhancing healthcare students' attitudes toward people living with dementia (PLWD). The main questions we intend to answer follow:

  • What are the attitudes toward PLWD, intentions to help PLWD, knowledge of dementia, and stigma of PLWD before and after participation in the gaming-based dementia education program?

  • What is the effect of gaming-based dementia education programs on enhancing attitudes toward PLWD?

Participants will volunteer for the class education program, which will last about 90 minutes. Participants can attend the class only once. This education program based on gaming tools will be structured with a lecture on dementia, N-impro (gaming tools), and bad/good short dramas. The gaming education program will be included in dementia-related courses.

Condition or Disease Intervention/Treatment Phase
  • Other: Health Education
N/A

Detailed Description

Participants in this study will be healthcare students at an Indonesian university (i.e., nursing students, public health students, etc.) enrolled in the semesters and courses designated for implementation of this educational program. For example, nursing students at Airlangga University will be among students in their fifth semester. Prospective participants will be given new ID numbers to ensure that their student ID numbers are undetected. The protocol for this study was reviewed and approved by an ethical committee of the Faculty of Nursing at Airlangga University.

Regarding recruitment, all candidate participants will be identified from the university's e-learning portal data. Students registered in the courses selected for implementation of this education program will have their data recorded at the beginning of the odd semester for the 2023/2024 academic year. Potentially eligible candidates will receive comprehensive study information and an invitation to participate.

The courses coordinator and Principal Investigator (PI) will explain the Semester Learning Plan and curriculum for the selected courses at the beginning of the semester. An overview of the research session's implementation will be presented, while detailed research procedures will be explained shortly before research is undertaken. An announcement regarding implementation of the research will be made approximately one week in advance, and recruitment will be carried out through Google Forms. Candidate participants will receive new IDs for this study and information about the schedule and location of the educational program through a class announcement three days prior.

On the intervention date, candidate participants will be present at the designated location and sign an attendance sheet using their new IDs. The PI will explain all stages of the study and reiterate regarding participants' freedom to withdraw at any time. The recruitment of study participants will not involve coercion. Students who choose not to participate in this study will still receive regular dementia-related materials through the university's e-learning portal, but they will not receive the game-based education program. Students who agree to participate in the study will provide informed consent. Further, participants in the educational program will complete a questionnaire before and after its implementation.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
400 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Other
Official Title:
Education Program for Enhancing Healthcare Students' Attitudes Toward People Living With Dementia
Anticipated Study Start Date :
Nov 22, 2023
Anticipated Primary Completion Date :
May 30, 2024
Anticipated Study Completion Date :
Jul 30, 2024

Arms and Interventions

Arm Intervention/Treatment
Other: A single-arm pre-post approach will be employed in this study;

There will be no control group. All participants will receive the same treatment. The intervention to be used will be a gaming education program conducted once with each participant.

Other: Health Education
As previously mentioned, the intervention for this study will be a gaming education program that will be conducted once with each participant. Implementation of the program will occur at different times. Each performance will include a maximum of 60 participants who will be divided into small groups within the same room. Seven to 10 participants will comprise a small group, and each group will have one facilitator. The facilitator will be either a member of the research team or a Health lecturer who will be recruited and trained by the Japanese and Indonesian research teams.

Outcome Measures

Primary Outcome Measures

  1. Attitude toward people living with dementia [Time Frame: 5-7 minutes for completion of the questionnaire]

    We will examine participants' attitudes toward people living with dementia with the Attitudes Toward People with Dementia Scale (Kim K, Kuroda K. Factors related to attitudes toward people with dementia development attitude toward dementia scale and dementia knowledge scale. Bulletin of Social Medicine. 2011; 28 (1), 43-55). The original study was published in Japanese. We performed forward-backwards translation to produce the Indonesian language version. The total number of items in the questionnaire is 14. This scale has a 4-point Linkert scale ranging from 1 (disagree) to 4 (agree). There consists of four subscales: tolerance (five items), refusal (four items), feeling of distance (three items), and affinity 8two items). The total score ranged from 14 to 56, with a higher score indicating a more favourable attitude.

Secondary Outcome Measures

  1. Knowledge of dementia [Time Frame: 5-7 minutes]

    Knowledge of dementia will be measured using 15 items of the Dementia-Related Knowledge Scale developed by (Kim & Kuroda, 2011), which assesses the knowledge of dementia, symptoms, treatments, and diagnosis of dementia. This dementia knowledge scale will ask respondents to answer with a 4-point Likert scale from disagree to agree. The author will calculate the total score of knowledge of dementia. The total score ranged from 15 to 60, with a higher score indicating a higher knowledge of dementia.

  2. Intention for helping behaviors toward people living with dementia [Time Frame: 2-3 minutes]

    To assess the Intention for helping behaviours toward people living with dementia, intended helping behaviours will be measured using four vignettes based on a previous study by Matsumoto et al. (2022). The vignettes describe situations in which people living with dementia may need assistance. Intended helping behaviours will be measured using a 4-point Likert scale (1= strongly disagree, 2= disagree, 3= agree, and 4= strongly agree). The higher score indicates a higher intention of helping behaviours people living with dementia.

  3. Fraboni's Scale of Ageism (FSA) [Time Frame: 5-7 minutes]

    To assess ageism associated with people living with dementia, we will use the Fraboni Scale of Ageism (FSA) short version of 19 items. The FSA short version consists of 19 items. That rate the negative opinion towards older people using the Likert scale (1= strongly disagree, 2= disagree, 3= agree, and 4= strongly agree). Statements representing positive rather than negative opinions towards older adults had reversed scoring (item numbers 13-16). Possible scores of FSA ranged from 19-76. The higher score indicates a higher level of ageism.

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:

Healthcare students enrolled in the designated semester and courses that align with the program's implementation

Exclusion Criteria: -

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Universitas Airlangga
  • Tokyo University
  • Kawasaki City College of Nursing

Investigators

  • Principal Investigator: Dianis Wulan Sari, Ph.D, Universitas Airlangga

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Dianis Wulan Sari, Principal Investigator, Universitas Airlangga
ClinicalTrials.gov Identifier:
NCT06122623
Other Study ID Numbers:
  • UAirlangga
First Posted:
Nov 8, 2023
Last Update Posted:
Nov 13, 2023
Last Verified:
Nov 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Dianis Wulan Sari, Principal Investigator, Universitas Airlangga
Additional relevant MeSH terms:

Study Results

No Results Posted as of Nov 13, 2023