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Completed

NCT Number: NCT02068534

A Qualitative and Quantitative Analysis on the Living History of Survivors From Charcoal-burning Suicide

The current study aims to explore the risk factors, protective factors, resilient factors, and factors jeopardizing the recovery progress on survivors from charcoal-burning suicide. To this end, an in-depth individual interview and Mini-Mental State Examination(MMSE) will be used to acquire the first-hand information on the attempters. As well, a more comprehensive neuropsychological test, WAIS III, will be administered at 3-month, 6-month, and 12-month after the index suicide attempt.

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Key information

Age range

20 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Far Eastern Memorial Hospital

New Taipei City, 220, Taiwan

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • above 20 years old, survivors from charcoal-burning suicide.

Exclusion criteria

  • under 20 years old
  • survivors from other kind of suicide
  • prisoner
  • suffer from a serious illness
  • foreigner/ can't speak Chinese
  • the people who can't express themselves
  • can not be interviewed in FEMH
  • people with severe physical or psychological symptoms

Treatment and study plan

Primary outcomes

  1. MMSE score

    Time frame: once

Sponsors and collaborators

Lead sponsor

Far Eastern Memorial Hospital

Other

Registry information

Important dates

Study start
2014
Primary completion
2014
Study completion
2014
First posted
Feb 21, 2014
Registry last updated
Jul 22, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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