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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT05968300
Other study ID # P0567396
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date March 20, 2024
Est. completion date August 31, 2024

Study information

Verified date June 2024
Source University of California, San Francisco
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The project is to facilitate pandemic recovery by promoting emotional wellness among Asian Californians. The intervention includes a 6-week program in which participants may choose to receive text only or text + Lay Health Worker outreach targeting 600 self-identified Asian Americans residing in California who speak/read English, Chinese, Korean, Hmong, or Vietnamese.


Description:

Investigators will conduct a non-randomized intervention trial (preference trial). Research participants involved in the trial will include 20 lay health workers (LHWs) and 600 trial participants with intervention delivered via SMS text messaging (for all participants), and the intervention group will receive educational intervention outreach from an LHW via Zoom or mutually agreed video conferencing online venues, and by telephone or instant messaging. Participants will choose which group they are in, SMS text messaging only or SMS text messaging plus educational outreach from an LHW.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 600
Est. completion date August 31, 2024
Est. primary completion date August 15, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: i) age 18 and older ii) speak Chinese, English, Hmong, Korean, or Vietnamese iii) self-identify as Asian American iv) have access to a mobile phone to receive SMS text messages Exclusion Criteria: - unwilling to receive SMS text messages from the project

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
INFORMED-Living Well
1) LHW outreach support providing responsive education and support; and 2) a 6-week automated SMS text messaging
Text Messaging Only
A 6-week automated SMS text messaging

Locations

Country Name City State
United States The Fresno Center Fresno California
United States Chinese Community Health Resource Center San Francisco California
United States University of California, San Francisco San Francisco California
United States Immigrant Resettlement & Cultural Center San Jose California

Sponsors (5)

Lead Sponsor Collaborator
University of California, San Francisco California Department of Public Health, Chinese Community Health Resource Center, University of California, Davis, University of California, Merced

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in decisional conflict scale (SURE) scores Self-assessed perceptions of decision conflict will be assessed using the 4-item Decision Conflict Scale (SURE). Scores on the SURE scale range from 0 to 4, with higher scores indicating less decisional conflict. A score of less than 4 indicates decisional conflict. Baseline and 8-week follow-up
Secondary Change in proportion of participants who have Intention to seek help for mental health We will use a survey item to assess participants' intention to seek help for mental health issues when needed. A response will be 0 (No) or 1 (Yes). Baseline and 8-week follow-up
Secondary Change in self-reported emotional wellness outcome We will use the four-item Patient Health Questionnaire (PHQ4) for measuring anxiety and depression symptoms. Scores are rated as normal (0-2), mild (3-5), moderate (6-8), and severe (9-12). Total score 3 or higher for the first 2 questions suggests anxiety, and total score 3 or higher for the last 2 questions suggests depression. Baseline and 8-week follow-up
Secondary Change in the percentage of participants' awareness of resources to get help or to learn more about improving emotional wellness We will assess participants' awareness of resources to get help or to learn more about improving emotional wellness. Two items created for the study will be used: 1) Do you know about "988"? (Yes, No, Unsure) 2) Do you know where to get help for mental health issues when you need to? (Yes, No, Unsure). The percentage of participants who answer "yes" to both questions will be assessed. Baseline and 8-week follow-up
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