Protocol of Multi-domain Attention Training

Status Completed

Clinical Trial Summary

This study sought to investigate the changes in attention in older adults with mild cognitive impairment after Multi-domain Attention Training .

Clinical Trial Description

This double-blind randomized controlled study has a 2-arm parallel group design. All subjects will be randomized by the block randomization, into intervention group (Multi-domain Attention Training, MAT), or active control group (Passive information activities, PIA). Training sessions of the MAT group are 45 minutes/day, 3 days/week, for 12 weeks (36 sessions each). The training of PIA group is the same as MAT group. The investigators constructed a rigorous MAT program adhering to the Consolidated Standards of Reporting Trials (CONSORT) reporting guidelines. The investigators expect to determine the improvement in attention function of older adults with mild cognitive impairment after using the MAT program. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT03379519
Study type	Interventional
Source	Ministry of Science and Technology, Taiwan
Contact
Status	Completed
Phase	N/A
Start date	August 1, 2016
Completion date	December 31, 2019

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