- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02096432
Suicide Prevention in Chinese Older Adults
December 20, 2022 updated by: Rush University Medical Center
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.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
54
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Illinois
-
Chicago, Illinois, United States, 60616
- Chinese community
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
48 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
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
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Behavioral: Behavioral Activation
Behavioral Activation includes the following components: empowering education, referral to treatment, care Management, and behavior activation
|
Behavioral Activation includes the following components: empowering education, referral to treatment, care Management, and behavior activation
|
Other: Usual Community Care
Community standard care as usual
|
Community standard care as usual
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Patient Health Questionnaire-9 (PHQ-9)
Time Frame: Outcome measure will be measured in 10 weeks' time
|
Outcome measure will be measured in 10 weeks' time
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: XinQi Dong, MD, MPH, Rush University Medical Center
- Principal Investigator: Melissa A. Simon, MD, MPH, Northwestern University
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
October 1, 2014
Primary Completion (Actual)
July 1, 2018
Study Completion (Actual)
November 1, 2018
Study Registration Dates
First Submitted
March 19, 2014
First Submitted That Met QC Criteria
March 21, 2014
First Posted (Estimate)
March 26, 2014
Study Record Updates
Last Update Posted (Estimate)
December 21, 2022
Last Update Submitted That Met QC Criteria
December 20, 2022
Last Verified
December 1, 2022
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 13110601
- R34MH100443 (U.S. NIH Grant/Contract)
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Suicidal Ideation
-
University of WashingtonUnited States Department of Defense; Military Suicide Research ConsortiumCompletedSuicidal and Self-injurious Behavior | Suicidal Ideation ActiveUnited States
-
The Catholic University of AmericaUniversity of Washington; VA Office of Research and DevelopmentCompletedSuicidal and Self-injurious Behavior | Suicidal Ideation Active
-
Emory UniversityGeorgia Institute of TechnologyCompletedSuicide, Suicidal IdeationUnited States
-
Henry M. Jackson Foundation for the Advancement...University of Pennsylvania; University of Michigan; Duke University; US Department... and other collaboratorsUnknownSuicide, Attempted | Suicidal Ideation ActiveUnited States
-
Technische Universität DresdenUnknownDepression | Suicidal Ideation/BehaviorGermany
-
International Islamic University, IslamabadRecruitingImpulsivity | Suicidal Ideation and BehaviorPakistan
-
VA Office of Research and DevelopmentCentral Texas Veterans Health Care SystemRecruitingHealth | Reintegration Difficulties | Suicidal Ideation and Behaviors | ConnectednessUnited States
-
Children's Hospital Medical Center, CincinnatiCompleted
-
Eisenhower Army Medical CenterAugusta University; The Geneva Foundation; Congressionally Directed Medical Research...CompletedSuicidal Ideation | Suicide | Suicidal Intention | Suicidal Impulses | Suicidal and Self-Injurious Behavior | Suicidal DepressionUnited States
-
Ohio State UniversityUniversity of Minnesota; Rutgers UniversityCompletedSuicidal Ideation | SuicidalUnited States
Clinical Trials on Behavior Activation
-
VA Office of Research and DevelopmentCompletedObsessive Compulsive Disorder | Generalized Anxiety Disorder | Major Depressive Disorder | Posttraumatic Stress Disorder | Panic Disorder | Social Phobia | Specific Phobia | Persistent Depressive DisorderUnited States
-
Texas Tech UniversityRecruitingGrief | Mental Health Issue | Burden, CaregiverUnited States
-
Texas Tech UniversityNot yet recruitingGrief | Mental Health Issue | Burden, CaregiverUnited States
-
Oregon Research InstituteNational Institute on Drug Abuse (NIDA)CompletedChildhood Disruptive Behavior ProblemsUnited States
-
Evidence-Based Practice Institute, Seattle, WACompletedDepression | Insomnia | SuicideUnited States
-
RANDGrand Challenges Canada; Danang Psychiatric Hospital; Basic Needs VietnamCompleted
-
Duke UniversityNational Cancer Institute (NCI); Memorial Sloan Kettering Cancer Center; Columbia... and other collaboratorsCompletedBreast Neoplasms | Early Detection of CancerUnited States
-
New York State Psychiatric InstituteCallen-Lorde Community Health CenterCompletedHIV Infection | FatigueUnited States
-
University of NebraskaCompletedChronic DiseaseUnited States
-
University of ChicagoNational Cancer Institute (NCI); The Hospital for Sick Children; Memorial Sloan... and other collaboratorsEnrolling by invitationColorectal Cancer | Early Detection of CancerUnited States