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Clinical Trials/NCT05803460
NCT05803460
Completed
Not Applicable

Explore the Effects of Virtual Reality Based Natural Environment Intervention Programs on Improving Attention, Emotion, and Cognitive Function of Older People

National Yang Ming Chiao Tung University1 site in 1 country120 target enrollmentApril 7, 2023
ConditionsOlder People

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Older People
Sponsor
National Yang Ming Chiao Tung University
Enrollment
120
Locations
1
Primary Endpoint
Trail Making Test
Status
Completed
Last Updated
4 months ago

Overview

Brief Summary

The objective of this study is to evaluate the effectiveness of virtual natural environment interventions on attention and mood among community-dwelling older adults in Taiwan. It was hypothesized that virtual reality combined with natural environments will improve attention to varying degrees and produce mood and physiological health outcomes in the elderly. This will be assessed by comparing the effects of virtual natural interventions with actual urban and natural interventions. Participants will randomly assign to virtual nature, actual nature, or actual urban group for a single 20-minute environmental session.

Detailed Description

This study will examine the effect of virtual natural environment intervention on attention and mood among community-dwelling older adults in Taiwan. This consist 3 parallel groups and 2 assessment periods. Participants in communities will be randomly assigned to virtual nature, actual nature, or actual urban group for a single 20-minute environmental session. Data will be collected at baseline and after intervention. This study recruits older adults from community locations in Taipei, Taiwan. Since no similar studies have been conducted before, the medium effect size 0. 25 is assumed, using the F-test analysis of variance, α = 0.05, power = 0.80, calculated the required total of 120 participants. Data is collected using mood and restorative questionnaires, attention tests, and a digital heart variability device. Statistical analyses will be performed using generalized estimating equations.

Registry
clinicaltrials.gov
Start Date
April 7, 2023
End Date
July 31, 2024
Last Updated
4 months ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Age 65 years and older
  • Cognitive function is normal (SPMSQ \>8)(The SPMSQ test was performed before the intervention to screen the cognitive function of the subjects).
  • The subjects can communicate in Chinese or Taiwanese.
  • Exclusion criteria:
  • Diseases affecting the results of the study, such as mental illness
  • Vision or hearing problems
  • Diseases transmitted by eyes or skin

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Trail Making Test

Time Frame: Baseline and 20 minutes

To measure attention.

The Positive and Negative Affect Schedule

Time Frame: Baseline and 20 minutes

To measure emotion.

Digit span test

Time Frame: Baseline and 20 minutes

To measure attention.

Secondary Outcomes

  • Blood pressure, heart rate and heart rate variability(Baseline and 20 minutes)

Study Sites (1)

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