- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04376515
Harnessing Online Peer Education Online Support Intervention for COVID-19 (HOPE COVID-19)
June 3, 2022 updated by: Sean D Young, University of California, Irvine
HOPE Intervention for COVID-19
The Harnessing Online Peer Education COVID-19 (HOPE COVID-19) intervention will assess whether a peer-led online support community can improve behavioral health outcomes related to COVID-19.
Study Overview
Status
Active, not recruiting
Conditions
Intervention / Treatment
Detailed Description
The Harnessing Online Peer Education COVID-19 (HOPE COVID-19) intervention will assess whether a peer-led online support community can improve behavioral health outcomes related to COVID-19.
Participants in the intervention group will be assigned to peer leaders trained in the HOPE intervention methods.
Study Type
Interventional
Enrollment (Actual)
120
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
-
-
California
-
Irvine, California, United States, 92617
- UC Irvine
-
-
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
18 years and older (ADULT, OLDER_ADULT)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- 18-30 years old
- English speakers only
- U.S. Resident
- Part of phase 1a or 1b of COVID-19 vaccine rollout (Healthcare personnel, education, and frontline essential workers, verified through LinkedIn profile)
- Uses social media and/or online communities greater than twice per week
- Has, or is willing to accept a friend request and group invite from our Facebook social media page
- Have not received a COVID-19 vaccine and do not have medical conditions or other circumstances preventing them from receiving one
Exclusion Criteria:
-
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
- Masking: SINGLE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
EXPERIMENTAL: HOPE Intervention
HOPE peer-led intervention
|
Online peer support community of peers trained in behavior change science
|
NO_INTERVENTION: Control
Control group- online community without peer leaders
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Requests for a COVID-19 Vaccine Resource Sheet
Time Frame: 1 time request during the 4-week study
|
Whether or not the participant requested that our study team send them an electronic resource sheet on the COVID-19 vaccine and where they can get vaccinated.
|
1 time request during the 4-week study
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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 (ACTUAL)
August 19, 2021
Primary Completion (ANTICIPATED)
December 18, 2022
Study Completion (ANTICIPATED)
December 1, 2023
Study Registration Dates
First Submitted
March 31, 2020
First Submitted That Met QC Criteria
May 5, 2020
First Posted (ACTUAL)
May 6, 2020
Study Record Updates
Last Update Posted (ACTUAL)
June 6, 2022
Last Update Submitted That Met QC Criteria
June 3, 2022
Last Verified
June 1, 2022
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- UCaliforniaIrvineSYoung No HS#
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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.
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