The Effect of Cognitive Function Training Program for Community Elderly

• Sponsor: Huie-Ling Chiu (Other)
• Overall Status: Completed
• CT.gov ID: NCT05353920
• Collaborator: (none)
• Enrollment: 62
• Location: 1
• Arms: 2
• Actual Duration (Months): 16.2
• Patients Per Site Per Month: 3.8

Study Details

Study Description

Brief 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.

Condition or Disease	Intervention/Treatment	Phase
Cognitive Function 1, Social	Other: Cognitive training	N/A

Study Design

• Study Type: Interventional
• Actual Enrollment: 62 participants
• Allocation: Randomized
• Intervention Model: Parallel Assignment
• Masking: Single (Participant)
• Primary Purpose: Supportive Care
• Official Title: The Effect of Cognitive Function Training Program for Community Elderly
• Actual Study Start Date: Dec 1, 2017
• Actual Primary Completion Date: Apr 1, 2019
• Actual Study Completion Date: Apr 8, 2019

Arms and Interventions

Arm	Intervention/Treatment
Experimental: Cognitive traiinig	Other: Cognitive training; cognitive related training bu virtual reality system
Active Comparator: Active control	Other: Cognitive training; cognitive related training bu virtual reality system

Outcome Measures

Primary Outcome Measures

1. MMSE [12 weeks]

   cognitive function

2. MoCA [12 weeks]

   cognitive function

Eligibility Criteria

Criteria

• Ages Eligible for Study: 65 Years and Older
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: Yes

Inclusion Criteria:

• 65 years old

Exclusion Criteria:

• TBI

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	TMU	Taipei		Taiwan

Sponsors and Collaborators

• Huie-Ling Chiu

Investigators

• Principal Investigator: Kuei-ru Chou, Professor

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.

• Responsible Party: Huie-Ling Chiu, Dr., Taipei Medical University
• ClinicalTrials.gov Identifier: NCT05353920
• Other Study ID Numbers: N201704031
• First Posted: Apr 29, 2022
• Last Update Posted: May 6, 2022
• Last Verified: Apr 1, 2022

• Individual Participant Data (IPD) Sharing Statement: Undecided
• Plan to Share IPD: Undecided
• Studies a U.S. FDA-regulated Drug Product: No
• Studies a U.S. FDA-regulated Device Product: No

Study Results

No Results Posted as of May 6, 2022