The Effect of Smartphone Push Notifications on Brain Power Score

February 26, 2019 updated by: HealthTech Connex Inc.

Assessing the Effect of Smartphone Push Notifications on Overall Score, Accuracy and Reaction Time of Brain Power Score

This study will examine how Brain Power Score, an objective measure of brain function, is affected by the presence of smartphone push notifications.

Study Overview

Status

Completed

Conditions

Detailed Description

Smartphones are a common device integrated into the lives of many individuals around the world. Researchers have previously found a relationship between mobile phone use and changes in brain activity, reaction times and sleep patterns.

Brain Power is a consumer-grade application using a proprietary combination of neurological (EEG) and behavioral (reaction time and accuracy) data to create a comprehensive score out of 1000 which allows users to have an objective evaluation of their brain performance.

This study will examine how Brain Power Score is affected by the presence of smartphone push notifications.

Study Type

Interventional

Enrollment (Actual)

40

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • British Columbia
      • Surrey, British Columbia, Canada, V3V 1Z2
        • HealthTech Connex Centre for Neurology Studies

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

19 years to 65 years (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Healthy volunteers
  • ≥19 years old
  • Must be proficient in English
  • Must be able to understand the study procedure and give informed consent

Exclusion Criteria:

  • Unable to provide informed consent

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Other
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Other: Push Notifications
Push notification number (0, 1, 3, 5) will be counter balanced within-subjects.
The purpose of this study is to assess how smartphone push notifications can impact the overall score, accuracy and reaction time of participants using the Brain Power Score application (app). Push notification quantity will be varied and counter-balanced.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Total Brain Power Score
Time Frame: 20 minutes
Brain Power Score combines neurological (EEG) and behavioral (reaction time and accuracy) data to create a comprehensive score out of 1000.
20 minutes

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Accuracy
Time Frame: 20 minutes
Percentage of correctly classified instances
20 minutes
Reaction time
Time Frame: 20 minutes
Time to respond to the stimulus (milliseconds)
20 minutes

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

August 14, 2018

Primary Completion (Actual)

August 24, 2018

Study Completion (Actual)

August 24, 2018

Study Registration Dates

First Submitted

August 1, 2018

First Submitted That Met QC Criteria

August 7, 2018

First Posted (Actual)

August 9, 2018

Study Record Updates

Last Update Posted (Actual)

February 27, 2019

Last Update Submitted That Met QC Criteria

February 26, 2019

Last Verified

February 1, 2019

More Information

Terms related to this study

Other Study ID Numbers

  • HTC-BPS-001

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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