- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04303637
The Impact of Phone Use on Everyday Outcomes
Study Overview
Status
Conditions
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
Enrollment (Anticipated)
Contacts and Locations
Study Locations
-
-
-
Singapore, Singapore, 138527
- Recruiting
- Yale-NUS College
-
Contact:
- Jean Liu, PhD
- Email: jeanliu@yale-nus.edu.sg
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
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
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
Sponsor
Investigators
- Principal Investigator: Jean Liu, PhD, Yale-NUS College
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- S-18-213
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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