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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02068534
Other study ID # 102122-F
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 2014
Est. completion date December 2014

Study information

Verified date July 2020
Source Far Eastern Memorial Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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.


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date December 2014
Est. primary completion date December 2014
Accepts healthy volunteers No
Gender All
Age group 20 Years and older
Eligibility 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

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Taiwan Far Eastern Memorial Hospital New Taipei City

Sponsors (1)

Lead Sponsor Collaborator
Far Eastern Memorial Hospital

Country where clinical trial is conducted

Taiwan, 

Outcome

Type Measure Description Time frame Safety issue
Primary MMSE score once
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