At a glance

ClinicalIndex Comparison Record

N/ACompleted· 262 enrolled

Drug / intervention

24-week SUDOKU Training Programme +1 morebehavioral

Likely dose

Not stated in record

Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT04913857

NCT04913857N/ACompleted

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New Wine in Old Bottle: the Effects of SUDOKU Mind Activation and Revitalizing Training (SMART) Program on Cognitive Function Among People With Mild Cognitive Impairment

The University of Hong Kong·interventional·Posted Jun 4, 2021·Updated Jan 9, 2024

In Brief

A clinical study evaluating 24-week SUDOKU Training Programme and Control Arm (wait-list) for Mild Cognitive Impairment. Completed, enrolled 262 participants across 1 site.

Detailed Summary

This study aims to implement a SUDOKU Mind Activation and Revitalization Training (SMART) Program to promote cognitive health among patients with mild cognitive impairment (MCI), and the use of active mind strategy in preventing dementia among the older adults. The SMART Program consists of two components including, a community empowerment-educational campaign on active mind strategies for older adults, and a 24-week SUDOKU Training Programme for people with MCI.

Study Details

Study Typeinterventional

Allocation--

Masking--

Primary Purpose--

ConditionsMild Cognitive Impairment

CountriesHong Kong

Collaborators--

Timeline

N/ACompletedFinished

202120222023202420252026

Enrollment StartSep 2020

First PostedJun 2021

Primary CompletionOct 2023

Study CompletionDec 2023

TodayJul 2026

First PostedJun 4, 2021

Enrollment StartSep 15, 2020

Primary CompletionOct 31, 2023

Study CompletionDec 31, 2023

TodayJul 2, 2026

Enrollment to primary: 3.1 yearsPosted 5.1 years ago

Interventions

24-week SUDOKU Training Programmebehavioral

12-week face-to-face training session and a 12-week facilitated self-practice

Control Arm (wait-list)other

wait-list comparison group will receive the same program upon completion of the 6-month posttest evaluation on study outcomes