NCT07160907

Brief Summary

This study aims to evaluate the effectiveness of an aging simulation experience course in enhancing the aging knowledge, care attitudes, empathy, communication skills, and learning satisfaction of care service personnel working in residential long-term care institutions.

Trial Health

57
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
162

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Oct 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

June 26, 2025

Completed
2 months until next milestone

First Posted

Study publicly available on registry

September 8, 2025

Completed
23 days until next milestone

Study Start

First participant enrolled

October 1, 2025

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2025

Completed
Last Updated

September 8, 2025

Status Verified

August 1, 2025

Enrollment Period

3 months

First QC Date

June 26, 2025

Last Update Submit

August 31, 2025

Conditions

Keywords

Ageing KnowledgeAttitudeEmpathyCommunication SkillsLearning Satisfaction

Outcome Measures

Primary Outcomes (5)

  • Aging Knowledge

    knowledge about Aging

    baseline, month 1、2

  • Attitudes

    attitudes towards aging

    baseline, month 1、2

  • Empathy

    Empathy for Aging

    baseline, month 1、2

  • Communication Skills

    Communication Skills for Aging

    baseline, month 1、2

  • Learning Satisfaction

    Learning satisfaction after class

    baseline, month 1、2

Study Arms (2)

Intervention group

EXPERIMENTAL

Participants in this group will receive a comprehensive ageing simulation training program, which includes: (1) an ageing knowledge and empathy-focused lecture incorporating interactive videos and scenario-based video discussions; (2) an ageing simulation activity using the "PengZu Suit" to mimic physical decline across five caregiving scenarios; and (3) a peer group discussion facilitated by empathy-trained professionals. This intervention aims to enhance participants' ageing knowledge, care attitudes, empathy, communication skills, and learning satisfaction.

Behavioral: Ageing Simulation Experience Program

Control group

ACTIVE COMPARATOR

Participants in this group will receive only the ageing knowledge lecture, which includes basic concepts of aging and empathy delivered through multimedia materials. They will not participate in the simulation activity or the peer discussion session.

Behavioral: Ageing Simulation Experience Program

Interventions

Ageing Simulation Experience Program is a structured training that includes a multimedia lecture, a hands-on aging simulation using the PengZu Suit, and a peer discussion. It aims to enhance care workers' aging knowledge, empathy, attitudes, and communication skills through experiential learning.

Control groupIntervention group

Eligibility Criteria

Age20 Years - 70 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Participants must be care workers currently employed at residential long-term care institutions in Eastern Taiwan, aged between 20 and 70 years. They must have at least one month of work experience in their current role, be literate, capable of completing written questionnaires, able to communicate in Mandarin or Taiwanese, and willing to provide informed consent to participate in the study.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Tzu Chi University

Hualien City, Taiwan

RECRUITING

MeSH Terms

Conditions

Behavior

Central Study Contacts

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
OTHER
Intervention Model
PARALLEL
Model Details: cluster randomised controlled trial
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
researcher

Study Record Dates

First Submitted

June 26, 2025

First Posted

September 8, 2025

Study Start

October 1, 2025

Primary Completion

December 31, 2025

Study Completion

December 31, 2025

Last Updated

September 8, 2025

Record last verified: 2025-08

Data Sharing

IPD Sharing
Will not share

Locations