- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05097807
The Impact of Shallow Reading in Social Media
The Short-term and Long-term Impact of Word-picture-based and Short Video-based Shallow Reading Behavior in Social Media
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Guangbin Cui, MD & PhD
- Phone Number: 86-29-84777863
- Email: cuigbtd@fmmu.edu.cn
Study Contact Backup
- Name: Wen Wang, MD & PhD
- Phone Number: 86-29-84778689
- Email: wangwen@fmmu.edu.cn
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Health volunteers
- Capable to use smartphone
Exclusion Criteria:
- Participants with a BMI greater than 30 or less than 18.5
- Any use of cigarettes or alcohol
- Color blindness
- Left-handedness
- With mental or psychiatric disorders
- With cognitive impairment
- Has a history of brain trauma
- Has a family history of psychiatric disorders
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: The impact of word-picture-based shallow reading in social media
Use Microblog on their smartphone, a word-picture-based social media service similar to twitter.
|
Participants are required to watch specific contents on their own smartphones.
|
Experimental: The impact of short video-based shallow reading in social media
Use Tiktok on their smartphone, a short video-based social media service.
|
Participants are required to watch specific contents on their own smartphones.
|
Active Comparator: The impact of full-length sci-fi novel reading
Read a full-length sci-fi novel (Three body) on their own smartphone.
|
Participants are required to watch specific contents on their own smartphones.
|
Active Comparator: The impact of film/TV series
Watch a film on their own smartphone.
|
Participants are required to watch specific contents on their own smartphones.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Dynamic change of sustained attention from baseline state to after 2 hours of social media use
Time Frame: Baseline state and after 2 hours
|
Continuous performance test (CPT) will be used to assess the difference of sustained attention before and after social media use. minimum: 0 maximum values: 1 Higher scores mean a better outcome. |
Baseline state and after 2 hours
|
Dynamic change of selective attention from baseline state to after 2 hours of social media use
Time Frame: Baseline state and after 2 hours
|
Stroop color word test (SCWT) will be used to assess the difference of selective attention before and after social media use. minimum: 0 maximum values: 1 Higher scores mean a better outcome. |
Baseline state and after 2 hours
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Cerebral blood flow changes from baseline state to after 2 hours of social media use
Time Frame: Baseline state and after 2 hours
|
Artery spin labeling (ASL) in MRI will be used to assess the difference of cerebral blood flow before and after social media use.
|
Baseline state and after 2 hours
|
Brain functional connectivity changes from baseline state to after 2 hours of social media use
Time Frame: Baseline state and after 2 hours
|
Blood oxygen level dependent (BOLD) in MRI will be used to assess the difference of functional connectivity before and after social media use.
|
Baseline state and after 2 hours
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Bo Hu, MD, Department of Radiology, Fourth Military Medical University
- Principal Investigator: YuTing Li, MD, Department of Radiology, Fourth Military Medical University
- Principal Investigator: JingTing Sun, MD, Department of Radiology, Fourth Military Medical University
- Principal Investigator: YuXuan Shang, MD, Department of Radiology, Fourth Military Medical University
Study record dates
Study Major Dates
Study Start (Anticipated)
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
Additional Relevant MeSH Terms
Other Study ID Numbers
- 202103129
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
IPD Sharing Time Frame
IPD Sharing Access Criteria
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- SAP
- ICF
- ANALYTIC_CODE
- CSR
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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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