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OpenTrials
Completed

NCT Number: NCT02096432

Suicide Prevention in Chinese Older Adults

This project aims to develop and refine a suicide intervention protocol, and pilot test a culturally tailored randomized control trial to reduce suicidal thoughts among U.S. Chinese older adults. During the first phase of the study, the investigators plan to invite the community advisory board and key stakeholders to participate in the iterative design and refinement of the study protocol. During the second phase of the project and after the initial screening and based on a specific set of inclusion criteria, the investigators will invite U.S. Chinese older adult to participate in a pilot randomized control trial of a culturally adapted intervention to reduce the frequency and intensity of suicidal thoughts in Chinese older adults. During the third phase of the project, the investigators plan to invite pilot intervention participants as well as key stakeholders and health care professionals on the cultural acceptability of the pilot intervention. Through the achievement of these objectives, the investigators will set the foundation to fully test a culturally adapted in-home intervention, which may be particularly suitable for Chinese older adults with suicidal thoughts as it addresses cultural-specific barriers and integrates care management within existing community services agencies using non-mental health professionals, including community health workers.

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Key information

Age range

50 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Chinese community

Chicago, Illinois, 60616, United States

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Self-identified as Chinese
  • >50 years of age
  • Suicidal thoughts within the last month as detected from the Item 9 in PHQ-9
  • No plans to move for 6 months
  • No significant cognitive impairment with Chinese Mini-Mental State Examination (C-MMSE) score >20

Treatment and study plan

Behavior Activation

Behavioral

Behavioral Activation includes the following components: empowering education, referral to treatment, care Management, and behavior activation

Usual Community Care

Behavioral

Community standard care as usual

Primary outcomes

  1. Patient Health Questionnaire-9 (PHQ-9)

    Time frame: Outcome measure will be measured in 10 weeks' time

Sponsors and collaborators

Lead sponsor

Rush University Medical Center

Other

Collaborators

  • National Institute of Mental Health (NIMH)
  • Northwestern University

Registry information

Important dates

Study start
2014
Primary completion
2018
Study completion
2018
First posted
Mar 26, 2014
Registry last updated
Dec 21, 2022

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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