- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05087654
3D VR and Hands-on Horticultural Activities Effects
October 8, 2021 updated by: National Taiwan Normal University
The Effects of a Combination of 3D Virtual Reality and Hands-on Horticultural Activities on Community-dwelling Older Adults' Mental Health: A Quasi-Experimental Study
This study aimed to explore the effects of a combination of 3D virtual reality (VR) and hands-on horticultural activities on the mental health of community-dwelling older adults.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Aging societies are of public health concern worldwide.
It is critical to develop strategies that harness technology to enhance older adults' mental health.
This study aimed to explore the effects of a combination of three-dimensional virtual reality (3D VR) and hands-on horticultural activities on the mental health of community-dwelling older adults.
Used a quasi-experimental design.
A total of 62 community-dwelling older adults were recruited.
The members of the experimental group participated in an 8-week intervention program.
Participants of both groups completed before-and-after intervention measurements for outcome variables that included perceived self-esteem, depression, isolation, mastery and achievement motives, which were analyzed using the generalized estimating equation (GEE).
This study found beneficial effects of a combination of 3D VR and hands-on horticultural activities on community-dwelling older adults' mental health.
Study Type
Interventional
Enrollment (Actual)
62
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
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Taipei, Taiwan, 106
- National Taiwan Normal University
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-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- ADULT
- OLDER_ADULT
- CHILD
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
Intact cognition, possessing the ability to understand verbal meaning and the ability to operate a VR joystick independently.
Exclusion Criteria:
A history of hand dysfunction, severe visual and hearing impairment, being allergic to plants or pollen, and a current illness such as epilepsy or stroke.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: OTHER
- Allocation: NON_RANDOMIZED
- Interventional Model: PARALLEL
- Masking: NONE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
EXPERIMENTAL: Experimental group
Received the Combination of 3D VR and Hands-on Horticultural Activities.
|
The intervention program consisted of 8 two-hour sessions that were conducted once a week for 8 consecutive weeks.
|
NO_INTERVENTION: Comparison group
Received scheduled activities, such as physical fitness, paper cutting, etc., without any gardening activities.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Self-esteem
Time Frame: about three months
|
Rosenberg Self-Esteem Scale consists of 14 items and each item is scored on a Likert-type scale that ranges from 1 (strongly agree) to 4 (strongly disagree), with higher scores indicating a higher level of self-esteem.
|
about three months
|
Depression
Time Frame: about three months
|
The Chinese version of the Geriatric Depression Scale was used, which has a total of 15 items.
All items were answered as either yes (1) or no (0).
The total raw scores ranged from 0 to 15, with a higher score indicating a higher level of depression.
|
about three months
|
Perceived isolation
Time Frame: about three months
|
A short-form scale of perceived isolation was used to measure isolation.
Each item was scored on a Likert-type scale from 1 (never) to 4 (often), with higher scores indicating a higher level of perceived isolation.
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about three months
|
Perceived mastery
Time Frame: about three months
|
The Chinese version of the Perceived Mastery Scale with a total of 7 items was used.
Each item was scored on a Likert-type scale from 1 (strongly agree) to 4 (strongly disagree).
The total raw score ranged from 7 to 28, with a higher score indicating a higher level of perceived mastery.
|
about three months
|
Achievement motives
Time Frame: about three months
|
The Achievement Motives Scale (AMS) consists of two kinds of motives, referred to as Motive to Achieve Success, (MAS) and Motive to Avoid Failure (MAF).
A short-form scale with 10 items was used to measure achievement motives, with 5 items each for MAS and MAF.
Each item was scored on a Likert-type scale from 1 (strongly agree) to 4 (strongly disagree).
|
about three months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (ACTUAL)
June 15, 2020
Primary Completion (ACTUAL)
October 27, 2020
Study Completion (ACTUAL)
December 31, 2020
Study Registration Dates
First Submitted
October 8, 2021
First Submitted That Met QC Criteria
October 8, 2021
First Posted (ACTUAL)
October 21, 2021
Study Record Updates
Last Update Posted (ACTUAL)
October 21, 2021
Last Update Submitted That Met QC Criteria
October 8, 2021
Last Verified
October 1, 2021
More Information
Terms related to this study
Other Study ID Numbers
- ECKIRB1090503
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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