NCT07547475

Brief Summary

With the increasing elderly population, nursing students' attitudes toward older adults and their levels of compassion competence have become increasingly important. While traditional educational methods may be insufficient in developing these skills, experiential learning approaches offer more effective outcomes. In particular, aging simulation applications enable students to understand the physical and emotional challenges experienced by older individuals, thereby enhancing their levels of empathy and compassion. The literature reports that simulation-based education has positive effects on attitudes and awareness. Therefore, the integration of aging simulation suits into nursing education is of great importance.

Trial Health

63
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Trial Health Score

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

Enrollment
102

participants targeted

Target at P50-P75 for not_applicable

Timeline
2mo left

Started Apr 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
not yet 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

Study Progress21%
Apr 2026Jun 2026

First Submitted

Initial submission to the registry

March 31, 2026

Completed
23 days until next milestone

First Posted

Study publicly available on registry

April 23, 2026

Completed
2 days until next milestone

Study Start

First participant enrolled

April 25, 2026

Completed
Same day until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 25, 2026

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

June 25, 2026

Expected
Last Updated

April 23, 2026

Status Verified

April 1, 2026

Enrollment Period

Same day

First QC Date

March 31, 2026

Last Update Submit

April 16, 2026

Conditions

Outcome Measures

Primary Outcomes (1)

  • "Compassion Competence Scale"

    11-item, 5-point Likert scale

    The primary metric will be completed within 1 day of data collection beginning.

Secondary Outcomes (1)

  • "Compassion Competence Scale"

    The outcome measure will be completed within 8 weeks of the start of data collection.

Study Arms (2)

control

NO INTERVENTION

"No intervention will be implemented; only the measurement scales will be administered."

intervention group

ACTIVE COMPARATOR

Students will be grouped based on pretest results obtained prior to the eight-week training program to ensure similar characteristics. Accordingly, after being stratified according to their pretest scores, participants will be randomly assigned to the experimental and control groups using a randomization method. The randomization process will be carried out using computer-based random number generation, and to prevent selection bias, the allocation will be performed by an individual independent of the research team. To ensure the impartiality of the assignment process, the randomization list will be concealed from the implementing researchers, and participants will not know in advance which group they will be assigned to. Within the scope of the study, the same training program will be applied to all participants, with the only difference between the groups being the use of an aging simulation suit in the experimental group.

Behavioral: aging simulation suit on nursing students'Behavioral: aging simulation suit on nursing students

Interventions

The population of the study will consist of third-year nursing students (N=110) enrolled in the Faculty of Health Sciences at Eastern Mediterranean University during the 2025-2026 spring semester. No sampling method will be applied; instead, all students who voluntarily agree to participate will constitute the sample of the study. Students will be grouped based on pretest results obtained prior to the eight-week training program to ensure similar characteristics. Accordingly, after being stratified according to their pretest scores, participants will be randomly assigned to the experimental and control groups using a randomization method. The randomization process will be carried out using computer-based random number generation, and to prevent selection bias, the allocation will be performed by an individual independent of the research team. To ensure the impartiality of the assignment process, the randomization list will be concealed from the implementing researchers, and participa

intervention group

Eligibility Criteria

Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

  • Being a third-year nursing student
  • Being enrolled in the HMSR 312 Geriatric Nursing course
  • Volunteering to participate in the study

You may not qualify if:

  • Having a physical condition that would prevent the use of an aging simulation suit
  • Having advanced orthopedic, neurological, or balance problems

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Eastern Mediterranean Univercity

Famagusta, Ammochostos, 99450, Cyprus

Location

Central Study Contacts

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
OTHER
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Senior İnstructor Dr. (Principal Investigator)

Study Record Dates

First Submitted

March 31, 2026

First Posted

April 23, 2026

Study Start

April 25, 2026

Primary Completion

April 25, 2026

Study Completion (Estimated)

June 25, 2026

Last Updated

April 23, 2026

Record last verified: 2026-04

Data Sharing

IPD Sharing
Will share

The ethical attitudes and compassion levels of nursing students toward older adults will be shared with all readers.

Locations