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NCT05353920 Clinical Trial

The Effect of Cognitive Function Training Program for Community Elderly

Cognitive Function 1, Social Clinical Trial

Official title:
The Effect of Cognitive Function Training Program for Community Elderly

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT05353920
Other study ID # N201704031
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date December 1, 2017
Est. completion date April 8, 2019

Study information
Verified date April 2022
Source Taipei Medical University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Background. Recently, cognitive function training program has been shown to improve cognitive function in elders. However, the effects of cognitive function training program on elderly living in the community have not been thoroughly evaluated. Objective. The purpose of this study is to construct and evaluate the effects of cognitive function training program on cognitive function for community elderly. Design. This is a randomized controlled study. Study subjects are elderly living in community. Subjects will be randomized into experimental group or active control group. The evaluation of the program will be evaluated at baseline, immediate after, 3 months, 6 months, and 1 year after the last session. The primary outcome indicators of the training is cognitive function, assessed by MMSE and MoCA. Expected contribution. With rigorous design and long term follow-up, the effectiveness of cognitive function training program in Chinese population in Taiwan can be evaluated. Results of the current study will determine the value of the cognitive function training program and provide valuable information for future utilization of this protocol.

Recruitment information / eligibility
Status Completed
Enrollment 62
Est. completion date April 8, 2019
Est. primary completion date April 1, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 65 Years and older
Eligibility Inclusion Criteria: - 65 years old Exclusion Criteria: - TBI

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• Cognitive training
cognitive related training bu virtual reality system

Locations
Country Name City State
Taiwan TMU Taipei

Sponsors (1)
Lead Sponsor Collaborator
Huie-Ling Chiu

Country where clinical trial is conducted

Taiwan, 

Outcome
Type Measure Description Time frame Safety issue
Primary MMSE cognitive function 12 weeks
Primary MoCA cognitive function 12 weeks
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