Boost Study 21270 (Cognition)

Status Completed

Clinical Trial Summary

This study is designed to to test the technical feasibility of encouraging interaction with a mobile smartphone software package (mHealth app) for training aspects of executive function and cognition.

Clinical Trial Description

The purpose of this human subjects study is to test the technical feasibility of interaction with a mobile smartphone software package (mHealth app) for training in aspects of executive function and cognition. The study participants are healthy subjects recruited online, with consent secured at the time of screening, and with enrollees assigned to High or Low groups on the basis of initial screening task scores. Subjects are requested to participate for at least 150 min per week in app interaction activities for up to 8 weeks with measures primarily evaluating feasibility of app package task completion, and secondarily evaluating the cognitive effect of these activities. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT05990335
Study type	Interventional
Source	NXTech
Contact
Status	Completed
Phase	Early Phase 1
Start date	April 18, 2022
Completion date	March 27, 2023

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