A Community Intervention Trial of Multimodal Suicide Prevention Program in Japan (NOCOMIT-J)

Japan Foundation for Neuroscience and Mental Health

Status: Completed

Conditions: Suicide

Treatments: Behavioral: Multimodal suicide prevention program; Behavioral: Suicide prevention program as usual

Study type: Interventional

Funder types: Other

Identifiers

NCT00737165

J-MISP-02

UMIN000000460 (Registry Identifier)

Details and patient eligibility

About

1. The primary goal for this study is to examine the effectiveness of community-based multimodal intervention program for suicide prevention in relatively high suicide rate region compared to control region.
2. The secondary goal for this study is to explore the effectiveness of community-based multimodal intervention program for suicide prevention in the highly populated regions. In addition, we examine the effectiveness of the prevention program in the all regions combined.

Full description

Suicide is a major public health problem and the number of suicide victims has exceeded 30,000 a year since 1998 in Japan. Suicide rate is almost 25/100,000, which are remarkably high numbers among advanced countries. To examine the effectiveness of community-based multimodal intervention program for suicide prevention, a trial by J-MISP (Japanese Multimodal Intervention Trials for Suicide Prevention). This research project is one of the strategic research projects funded by The Japanese Ministry of Health, Labor and Welfare.

Enrollment: 1,951,060 patients

Sex: All

Volunteers: No Healthy Volunteers

Inclusion criteria

• Areas which meet the following criteria are eligible for this study;

  • An area with firm support from local government and other organizations to conduct this multimodal suicide prevention program
  • An area capable to select intervention and control regions
  • An area capable to follow the data collection procedure described in the protocol
  • An area with comparable baseline data on suicide attempts rate in intervention and control region
  • An area with comparable baseline data on demographics in intervention and control region

Exclusion criteria

• None

Trial design

Primary purpose: Prevention

Allocation: Non-Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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1,951,060 participants in 2 patient groups

Multimodal community intervention

Experimental group

Description:

Multimodal suicide prevention program

Treatment:

Behavioral: Multimodal suicide prevention program

Community intervention as usual

Active Comparator group

Description:

Suicide prevention program as usual

Treatment:

Behavioral: Suicide prevention program as usual