The Impact of Phone Use on Everyday Outcomes

March 10, 2020 updated by: Jean Liu, Yale-NUS College
Participants will download a phone-tracking app for a week to track phone usage, providing objective data on usage patterns. Quantitative tasks and questionnaires will also be carried out before and after the tracking period.

Study Overview

Status

Unknown

Intervention / Treatment

Detailed Description

A notable shortcoming of existing mobile phone research is that 'phone use' has almost exclusively been measured through subjective reports - by simply asking respondents how much time they spend on their mobile phones each day. This operational definition, however, is a major shortcoming as phone use is difficult to track - and is thus likely to be highly inaccurate.

To address this gap, the investigators describe in this proposal a first step to characterize phone usage in an objective manner - by asking adolescents to download a phone-tracking app for a week. This circumvents measurement errors inherent to self-reports, and allows us to probe: (1) how accurate adolescents' estimates are of their own phone usage, and (2) whether objective phone usage predicts any cognitive, socio-emotional, or physical outcomes. The completion of this study will represent an important step forward in the development of empirically-driven guidelines on phone use amongst adolescents.

Study Type

Observational

Enrollment (Anticipated)

1000

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

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

13 years to 18 years (Child, Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Adolescents aged 13-18 years old recruited from Singapore schools.

Description

Inclusion Criteria:

  • Owns a smartphone

Exclusion Criteria:

  • Parents not willing to give consent
  • History of medical or psychiatric disorder
  • History of motion sickness, dizziness or epilepsy

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

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
High school student
13-18 year old students enrolled in schools within Singapore.
Objective and subjective reports of smartphone use (e.g., number of hours, number of pick-ups, how phones are used)

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Depression Anxiety Stress Scale (DASS 21)
Time Frame: 11 minutes (single measurement)
A 21-item, 4-point scale measuring participant emotional states. This is the short form of the longer 42-item DASS.
11 minutes (single measurement)
Body mass index
Time Frame: 1 minute (single measurement)
Participants' body mass index
1 minute (single measurement)
Sleep duration
Time Frame: 2 minute (single measurement)
Assessment of participants' sleep time & wake time
2 minute (single measurement)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Digit Span Task
Time Frame: 10 minutes (single measurement)
A digit span task carried out using a computer program
10 minutes (single measurement)
Psychomotor Vigilance Task
Time Frame: 10 minutes (single measurement)
PVT carried out using a computer program
10 minutes (single measurement)
Pediatric Daytime Sleepiness Scale (PDSS)
Time Frame: 5 minutes (single measurement)
A 8-item, 5-point self-report scale to measure sleepiness during the day.
5 minutes (single measurement)
Strengths and Difficulties Questionnaire (SDQ)
Time Frame: 10 minutes (single measurement)
A questionnaire looking at a student's emotional and behavioural aspects in relation to coping with school.
10 minutes (single measurement)

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
General Questionnaire on Media Consumption
Time Frame: 5 minutes (single measurement)
A short questionnaire on the usage patterns of various media devices.
5 minutes (single measurement)
Subjective Report of Phone Usage
Time Frame: 10 minutes (single measurement)
A 5-item questionnaire that collects data on self-reported phone use patterns.
10 minutes (single measurement)

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Jean Liu, PhD, Yale-NUS College

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)

March 25, 2019

Primary Completion (Anticipated)

May 31, 2021

Study Completion (Anticipated)

June 10, 2021

Study Registration Dates

First Submitted

March 8, 2020

First Submitted That Met QC Criteria

March 10, 2020

First Posted (Actual)

March 11, 2020

Study Record Updates

Last Update Posted (Actual)

March 11, 2020

Last Update Submitted That Met QC Criteria

March 10, 2020

Last Verified

March 1, 2020

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • S-18-213

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

Stipulations by the institutional review board do not allow individualized data to be shared.

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.

Clinical Trials on Depression

Clinical Trials on Phone use

Subscribe