Home-Based Exergame Program for Community-Dwelling Older Adults

Frail Elderly Clinical Trial

Official title:

Home-Based Exergame Program for Community-Dwelling Older Adults

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05802537
• Other study ID #: 1041455-202302-HR-003-01
• Status: Completed
• Phase: N/A
• Start date: November 1, 2022
• Est. completion date: January 13, 2023

Study information

• Verified date: March 2023
• Source: Kyungdong University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study was to investigate the effect of a home-based exergame program on physical function, fall efficacy, depression, and quality of life in older adults. For the purpose of the study, we established the following hypotheses. Older adults who participate in a home-based exergame program will experience significant improvements in physical function, fall efficacy, depression, and quality of life compared to those who do not participate in the program.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 60
• Est. completion date: January 13, 2023
• Est. primary completion date: November 7, 2022
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 75 Years and older

Eligibility

Inclusion Criteria:

• 75 years or older

• the ability to walk independently with or without a walking aid

• a mini-mental state examination score = 24.

Exclusion Criteria:

• musculoskeletal disorders such as fractures or dislocations

• neurological impairment

• mental disorders

• uncontrolled endocrine, cardiovascular, or urinary system diseases

Related Conditions & MeSH terms

• Frail Elderly

Intervention

Other:
• Home-based exergame program
The home-based exergame program was conducted at the participants' homes for 50 min, three times a week, for eight weeks. Online education on fall prevention and musculoskeletal health management was provided once a week for 50 minutes, one day a week, for 8 weeks.

Locations

Country	Name	City	State
Korea, Republic of	Kyungdong University	Wonju	Gangwon-do

Sponsors (1)

Lead Sponsor	Collaborator
Kyungdong University

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	One-leg standing test	The one-leg standing test was used to evaluate static postural balance. The one-leg standing test is a simple, reliable, and valid test for assessing balance and fall risk in older adults.	Change from baseline after intervention at 8 weeks
Primary	Berg balance scale	To evaluate dynamic postural balance, the Berg balance scale was used. It has a perfect score of 56 and consists of 14 items, with a perfect score of 4 for each item.	Change from baseline after intervention at 8 weeks
Primary	Functional reaching test	Functional reaching test was used to evaluate movement limits.	Change from baseline after intervention at 8 weeks
Primary	Timed up-and-go test	Timed up-and-go test was used to assess functional movement and mobility.	Change from baseline after intervention at 8 weeks
Primary	Five-times sit-to-stand test	Five-times sit-to-stand test was used to evaluate lower-extremity muscle strength.	Change from baseline after intervention at 8 weeks
Secondary	Falls Efficacy	The modified falls efficacy scale, which was developed for older adults specifically, was used to evaluate the fall efficacy.	Change from baseline after intervention at 8 weeks
Secondary	Depression	Depression was measured using the geriatric depression scale.	Change from baseline after intervention at 8 weeks
Secondary	Health-Related Quality of Life	The 36-item short-form health survey was used to measure health-related quality of life.	Change from baseline after intervention at 8 weeks