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Clinical Trials/NCT05968300
NCT05968300
Completed
Not Applicable

Getting INFORMED and Living Well: A Demonstration Project to Facilitate Pandemic Recovery Among Asian Americans in California

University of California, San Francisco4 sites in 1 country616 target enrollmentMarch 20, 2024

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
COVID-19
Sponsor
University of California, San Francisco
Enrollment
616
Locations
4
Primary Endpoint
Change in decisional conflict scale (SURE) scores
Status
Completed
Last Updated
last year

Overview

Brief 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.

Detailed 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.

Registry
clinicaltrials.gov
Start Date
March 20, 2024
End Date
August 31, 2024
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

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

Outcomes

Primary Outcomes

Change in decisional conflict scale (SURE) scores

Time Frame: Baseline and 8-week follow-up

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.

Secondary Outcomes

  • Change in the percentage of participants' awareness of resources to get help or to learn more about improving emotional wellness(Baseline and 8-week follow-up)
  • Change in self-reported emotional wellness outcome(Baseline and 8-week follow-up)
  • Change in proportion of participants who have Intention to seek help for mental health(Baseline and 8-week follow-up)

Study Sites (4)

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