Skip to main content
Clinical Trials/NCT04984694
NCT04984694
Completed
Not Applicable

Evaluation of Computerized Virtual Reality on FunctionalAbility and Quality of Life in Elderly

Taipei Medical University1 site in 1 country45 target enrollmentFebruary 3, 2017

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Cognitive Dysfunction
Sponsor
Taipei Medical University
Enrollment
45
Locations
1
Primary Endpoint
Cognition-Global cognition
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

The number of dementia patients increased with aging population. People with subjective memory complaints or mild cognitive impairment (MCI) may have a high risk of developing dementia. Cognitive /memory training programs have shown the potential positive effects for improving or maintaining the cognitive progression. However, the impact of those cognitive progressions on functional ability and quality of life is not well understood. In addition, it appears to have large variability responsiveness among trained subjects. Most studies did not examine the individual difference associated with training. The major aim will evaluate the cognitive training programs on functional ability and quality of life in older adults. The results will be expected to understand the effectiveness of the computerized virtual reality training, improving or maintaining cognition, physical and psychosocial function, enhancing quality of life, and reducing the risk of developing disability even conversion into dementia in later life.

Detailed Description

Prevention strategies for dementia are needed because of the increasing prevalence of dementia. People with mild cognitive impairment are at high risk of developing a disability, even conversion into dementia in later life. Cognitive /memory training programs have shown the potential positive effects for improving or maintaining the cognitive progression. However, the impact of those cognitive progressions on functional ability and quality of life is not well understood. The major aim of this total project is to evaluate the short and long-term effects of computerized virtual reality training programs (Xavix Hot-Plus) on functional ability (cognition, physical and psychosocial function) and quality of life in older adults with mild cognitive impairment. The experimental research design with three groups, one pretest and four posttests will be conducted to examine the short-term and long-term effects on cognition (primary outcome), physical (secondary outcome), psychosocial function (secondary outcome), and quality of life (secondary outcome). Independent adults will be recruited from the community base on sample criteria. The total subjects will be 160 to 190 older adults and the community care centers include all eligible participants will be randomly assigned into computerized virtual reality training programs group (Hot-Plus group) or social interaction group. The subjects for the control group will be recruited in the community and be referred by neurological, psychiatric, or gerontological physicians. Participants who are in the Hot-Plus group will divide several small groups which will be 4 persons with mild cognitive impairment. Participants will receive a computerized virtual reality training program by Hot-Plus as a group activity one hour, once a week for 12 weeks. The participants in the social interaction group will come as a group for social interaction one hour weekly for 12 weeks. The control group will maintain their regular activities. Data will be analysed by using SPSS version 18.0 (SPSS, Chicago, IL), with the significance level is set at p\< .05. The normal distribution of the data will be evaluated using the Kolmogorov-Smirnov test. Mean, Standard deviation, frequency, and percentage will be performed to describe all variables. One-way analysis of variance (ANOVA) will be used to evaluate differences between groups according to the continuous variables, non-normal distribution of data will be calculated by Kruskasl-Wallis test. The chi-square test will be used for the comparison of categorical variables, and Fisher's exact test will be used due to the expected value less than four. Generalised Estimating Equation (GEE) will be used to examine the main effects, time effects, and interactions in outcomes over time. The results will be expected to understand the effectiveness of the computerized virtual reality training, improving or maintaining cognition, physical, psychosocial function, enhancing quality of life, and reducing the risk of developing disability even conversion into dementia in later life.

Registry
clinicaltrials.gov
Start Date
February 3, 2017
End Date
March 6, 2019
Last Updated
4 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Equal to or older than 60 years old
  • The SPMSQ scores range from 4-7 ( illiterate: 4-5, elementary: 5-6, junior high school: 6-7) or Clinical Dementia Rating Scale (CDR): 0.5
  • Be able to communicate in Mandarin or Taiwanese
  • Has the ability to see and hear well enough to follow the instructions
  • Agree to participate in this study.

Exclusion Criteria

  • Activity restrictions from physician recommendation
  • Unstable disease progress could affect their participation
  • Surgery for joints or spinal cord within 6 months
  • Unable to walk 50 meters with the assistant device
  • Learning disability

Outcomes

Primary Outcomes

Cognition-Global cognition

Time Frame: At 24 weeks after intervention.

Global cognition was measured by the Mini-Mental State Examination (MMSE), a modified version of a neuropsychological battery in the Consortium to Establish a Registry for Alzheimer's Disease (CERAD), which maximum score was 30 including orientation, memory, concentration, language, and praxis (Folstein, Folstein, \& McHugh, 1975; Morris et al., 1989).

Cognition-executive function

Time Frame: At 24 weeks after intervention.

Executive function was measured by the Stroop Color and Word Test (SCWT)(Golden et al., 2002). It consisted of three subtasks: word reading (RED, GREEN, and BLUE), color naming (XXXX's colored in red, green, or blue ink), and incongruent color-word naming (the words RED, GREEN, and BLUE printed in not matching red, green, or blue ink).

Cognition-memory

Time Frame: At 24 weeks after intervention.

Memory was measured by the Word List test, contained three types as following (Morris et al., 1989; Welsh et al., 1994): 1) Immediately recall; 2) Delayed recall; 3) Recognition.

Cognition-attention

Time Frame: At 24 weeks after intervention.

Attention was measured by the Digit Span (DS) subtest from the Taiwan version of the Wechsler Adult Intelligence Scale-Ⅲ (WAIS-IV; Wechsler, 2002), which contained two components: DS forward and DS backward.

Cognition-visual/spatial function

Time Frame: At 24 weeks after intervention.

Visual/spatial function was measured by the Clock Drawing Test (CDT). Participants were asked to draw a clock face, place all the numbers on it, and set the time to 11 past 10 (Powlishta et al., 2002; Shulman, Shedletsky, \& Silver, 1986).

Secondary Outcomes

  • Physical function-senior fitness test (SFT)(At 24 weeks after intervention.)
  • Physical function-IADL(At 24 weeks after intervention.)
  • Quality of Life-EQ5D-visual analogue scale(At 24 weeks after intervention.)
  • Psychosocial factors-Interpersonal Relationship Scale (IRS)(At 24 weeks after intervention.)
  • Physical function-unipedal stance test (UST)(At 24 weeks after intervention.)
  • Psychosocial factors-Global Well-Being Scale (GWBS)(At 24 weeks after intervention.)
  • Psychosocial factors-Geriatric Depression Scale-Short Form (GDS-SF)(At 24 weeks after intervention.)
  • Quality of Life-EQ5D-Utility(At 24 weeks after intervention.)

Study Sites (1)

Loading locations...

Similar Trials