Study on the Relationship Between Mobile Phone Addiction and Functional Gastrointestinal Disorders

Exploration of the Relationship Between Mobile Phone Addiction and Functional Gastrointestinal Disorders, a Cross-sectional Study

A cross-sectional study was conducted to collect the relevant data of college students' mobile phone addiction and FGIDs (IBS, FD) in the form of questionnaire, so as to understand the situation of college students' mobile phone addiction and the incidence of FGIDs (IBS and FD), and explore the correlation, so as to provide new ideas and scientific basis for the prevention, diagnosis and treatment of FGIDs among college students.

Study Overview

Status

Completed

Detailed Description

This study adopts the method of cross-sectional survey to collect the relevant data of Chinese college students' mobile phone addiction and FGIDs (IBS, FD) in the form of online and face-to-face questionnaire, so as to understand the situation of Chinese college students' mobile phone addiction and the incidence of FGIDs (IBS, FD), and explore the correlation, so as to provide new ideas and scientific basis for the prevention, diagnosis and treatment of FGIDs.

Study Type

Observational

Enrollment (Actual)

3000

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

    • Shaanxi
      • Xi'an, Shaanxi, China, 710004
        • The Second Affiliated Hospital of Xi'an Jiaotong University

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

17 years and older (Child, Adult, Older Adult)

Accepts Healthy Volunteers

N/A

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

College students over the age of 17 across the country

Description

Inclusion Criteria:

  • College students from all over the country, over 17 years old, have a physical examination before entering school
  • Sign the informed consent form, voluntarily participate and fill in the questionnaire

Exclusion Criteria:

  • People with diabetes, hyperthyroidism or hypothyroidism, peptic ulcer, inflammatory bowel disease, digestive tract tumor or severe medical and surgical disease
  • History of abdominal surgery (such as esophagus, stomach, small intestine, colon, rectum, appendix, gallbladder, hysterectomy, cesarean section)
  • Recently, there are some alarm symptoms, such as relieving black stool, bloody stool, hematemesis, abnormal anemia, fever, abnormal weight loss (no intention to lose weight, weight loss 5 kg in 3 months), change of defecation habits, dysphagia and so on
  • In the past 4 weeks, he has taken drugs that affect the judgment of gastrointestinal symptoms, such as anti-inflammatory painkillers, diazepam drugs, anti-anxiety drugs, depressants and so on

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

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Incidence of irritable bowel syndrome among College Students.Risk factors of irritable bowel syndrome.
Time Frame: 2020.07.03-2020.12.28
The irritable bowel syndrome was diagnosed by the Rome IV diagnostic questionnaire, and then the incidence of irritable bowel syndrome was calculated by SPSS. Through PHQ-9 questionnaire to diagnose depression, GAD-7 questionnaire to diagnose anxiety, MPAI questionnaire to diagnose mobile phone addiction, AIS questionnaire to diagnose insomnia, logistic regression analysis to calculate OR value and P value, to understand the relationship between irritable bowel syndrome and anxiety, depression, insomnia, mobile phone addiction.
2020.07.03-2020.12.28

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Incidence of functional dyspepsia among College Students.Risk factors of functional dyspepsia.
Time Frame: 2020.07.03-2020.12.28
The functional dyspepsia was diagnosed by the Rome IV diagnostic questionnaire, and then the incidence of functional dyspepsia was calculated by SPSS. Through PHQ-9 questionnaire to diagnose depression, GAD-7 questionnaire to diagnose anxiety, MPAI questionnaire to diagnose mobile phone addiction, AIS questionnaire to diagnose insomnia, logistic regression analysis to calculate OR value and P value, to understand the relationship between functional dyspepsia and anxiety, depression, insomnia, mobile phone addiction.
2020.07.03-2020.12.28

Collaborators and Investigators

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

Investigators

  • Study Director: jinhai Wang, MD, Second Affilated Hospital of Xi'an Jiaotong University

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)

July 1, 2020

Primary Completion (Actual)

December 28, 2020

Study Completion (Actual)

December 28, 2020

Study Registration Dates

First Submitted

July 3, 2020

First Submitted That Met QC Criteria

March 23, 2021

First Posted (Actual)

March 26, 2021

Study Record Updates

Last Update Posted (Actual)

March 26, 2021

Last Update Submitted That Met QC Criteria

March 23, 2021

Last Verified

March 1, 2021

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

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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