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NYC Community Engagement Alliance (NYCEAL) Against COVID-19 Disparities

Status: Recruiting
Location: See location...
Intervention Type: Behavioral
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Established in 2021, NYCEAL consists of approximately 40 organizational partners and 120 Community Health Workers (CHWs). Over the next four years (2024-2028), NYCEAL will work with this network to implement the following intervention: Building Community Resilience Program (BCR). To assess the impact of this intervention, an implementation research framework will be used, and pre- and post-surveys conducted, and other process evaluation measures collected. Changes in outcomes measures such as stress, resilience, overall wellbeing, and other related outcomes for participants in the BCR program will be measured for community healthcare workers and/or frontline workers that receive educational workshops.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: t
View:

• Able to consent

• Able to fill out the screening RedCap short survey

• Have access to a computer or smart gadget that will allow participant to be able to join the zoom call

• English speaking

• Living in NYC (5 boroughs)

• 18+ years of age (no upper bound age limit)

• Working with an NYCEAL CBO participating in BCR programming

Locations
United States
New York
Icahn School of Medicine at Mount Sinai
RECRUITING
New York
Contact Information
Primary
Devin Madden, PhD, MPH
devin.madden@mountsinai.org
212-659-9552
Backup
Nita Vangeepuram, MD, MPH
nita.vangeepuram@mssm.edu
Time Frame
Start Date: 2024-12-11
Estimated Completion Date: 2027-11-15
Participants
Target number of participants: 168
Treatments
Experimental: Immediate Intervention Group (First Cohort)
The first cohort of up to 36 participants will complete two surveys: a baseline survey within one month before the workshops begin, and a post-test survey within one month after the final workshop (approximately 8 months total from first to last survey)
Experimental: Waitlist Group (Second Cohort)
The second cohort of up to 36 participants will complete four surveys: two surveys in year 1 (matching the timing of the first cohort's surveys to serve as a control group), and two additional surveys in year 2 when they receive the intervention (a baseline survey within one month before their workshops begin, and a post-test survey within one month after their final workshop).
Related Therapeutic Areas
Sponsors
Leads: Icahn School of Medicine at Mount Sinai

This content was sourced from clinicaltrials.gov