Influential Path of Social Risk Factors toward Suicidal Behavior-Evidence from Chinese Sina Weibo Users 2013-2018. Academic Article uri icon

Overview

abstract

  • (1) Purpose: The purpose of this study was to determine suicidal risk factors, the relationship and the underlying mechanism between social variables and suicidal behavior. We hope to provide empirical support for the future suicide prevention of social media users at the social level. (2) Methods: The path analysis model with psychache as the mediate variable was constructed to analyze the relationship between suicidal behavior and selected social macro variables. The data for our research was taken from the Chinese Suicide Dictionary, Moral Foundation Dictionary, Cultural Value Dictionary and National Bureau of Statistics. (3) Results: The path analysis model was an adequate representation of the data. With the mediator psychache, higher authority vice, individualism, and disposable income of residents significantly predicted less suicidal behavior. Purity vice, collectivism, and proportion of the primary industry had positive significant effect on suicidal behavior via the mediator psychache. The coefficients of harm vice, fairness vice, ingroup vice, public transport and car for every 10,000 people, urban population density, gross domestic product (GDP), urban registered unemployment rate, and crude divorce rate were not significant. Furthermore, we applied the model to three major economic development belts in China. The model's result meant different economic zones had no influence on the model designed in our study. (4) Conclusions: Our evidence informs population-based suicide prevention policymakers that incorporating some social factors like authority vice, individualism, etc. can help prevent suicidal ideation in China.

publication date

  • March 5, 2021

Research

keywords

  • Social Media
  • Suicide

Identity

PubMed Central ID

  • PMC7967660

Scopus Document Identifier

  • 85101991474

Digital Object Identifier (DOI)

  • 10.3390/ijerph18052604

PubMed ID

  • 33807764

Additional Document Info

volume

  • 18

issue

  • 5