- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05451511
COVID-19 Resource Offers Among Rent and Utility Assistance Applicants in St. Louis
November 29, 2022 updated by: Matthew Kreuter, Washington University School of Medicine
Rapid Acceleration of Diagnostics Underserved Populations Supplement Rent Relief and COVID-19 in St. Louis: COVID-19 Resource Offers Among Rent and Utility Assistance Applicants in St. Louis
The purpose of this study is to evaluate health messaging strategies that help individuals with a high degree of housing-related needs engage in COVID-19 vaccination and testing behaviors.
Findings from this research can help other communities determine how best to integrate social needs and COVID-19 prevention services.
Participants' contact information will be shared with us by 211 with the participants' previously given consent.
The study team will send via text message a link to a survey that includes a screen where they will provide informed consent.
Those who provide consent will be randomly assigned to receive one of two surveys.
The order of the offers is what varies across the surveys.
Participants will be asked, along with other survey items, if they have been vaccinated against COVID-19.
If they have not, they will be asked if they are interested in receiving help to receive a vaccine.
Participants will also be asked if they are interested in receiving an at-home COVID self-test.
If they say yes to assistance with vaccination, a vaccine navigator will call and assist them.
If they say yes to receiving a COVID test, the study team will ship them a test that has been procured from the City of St. Louis Mayor's office.
One month later participants will be sent a follow-up survey that asks about their experiences either with testing or with vaccination if applicable.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
531
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
-
-
Missouri
-
Saint Louis, Missouri, United States, 63130
- Washington University in St. Louis
-
-
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:
- Applicants for rent and utility assistance in St. Louis City or County
- English language proficiency
- Be willing to be contacted via text message or email
- Resident of St. Louis City or County
Exclusion Criteria:
- N/A
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: Health Services Research
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Door-In-The-Face Technique
Using sequential request strategies, participants randomized to the Door-In-The-Face Technique group will be asked if they would like vaccination support (if not already vaccinated) and if they say no, they will be asked if they'd like to try a COVID-19 self-test at home.
|
Sequential request strategies will be applied as an intervention.
For the Door-In-The-Face Technique, participants first receive a large request they are unlikely to accept, followed by a smaller request that is the true behavior of interest.
|
|
Active Comparator: Foot-In-The-Door Technique
Using sequential request strategies, participants randomized to the Foot-In-The-Door Technique group will be first asked if they are interested in trying an at-home COVID-19 test and then asked if they are interested in vaccination support (if not already vaccinated).
|
Sequential request strategies will be applied as an intervention.
For the Foot-In-The-Door Technique, participants are shown an easier first request that they are likely to accept, followed by a larger request that is not the behavior of interest.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Proportion Vaccinated
Time Frame: Baseline
|
Via a mobile-optimized web-based survey, the investigators will ask individuals seeking rental/housing assistance if they are thinking about getting vaccinated and report the proportion "already vaccinated."
|
Baseline
|
|
Sequential Request Strategy Effectiveness
Time Frame: Baseline
|
To compare differences in testing acceptance and vaccination responses by sequential request strategy, the investigators will identify which strategy is associated with greater testing and vaccination intentions.
|
Baseline
|
|
Testing and Vaccination Offer Acceptance
Time Frame: Baseline
|
At baseline, participants will be offered vaccination support and free a COVID-19 self-test.
The investigators will report the proportion of applicants who accept each of the offers.
|
Baseline
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Testing and Vaccination Behaviors
Time Frame: 1 month follow-up
|
After one month follow-up, the investigators will report the proportion of participants who complete the self-test and report the results, and report having been vaccinated since the baseline survey.
|
1 month follow-up
|
|
Rent Relief
Time Frame: Baseline
|
The investigators will ask about the outcome of rent or utility assistance.
|
Baseline
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
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)
July 5, 2022
Primary Completion (Actual)
September 25, 2022
Study Completion (Actual)
September 25, 2022
Study Registration Dates
First Submitted
July 7, 2022
First Submitted That Met QC Criteria
July 7, 2022
First Posted (Actual)
July 11, 2022
Study Record Updates
Last Update Posted (Actual)
November 30, 2022
Last Update Submitted That Met QC Criteria
November 29, 2022
Last Verified
November 1, 2022
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 3R01CA235773-03S2 (U.S. NIH Grant/Contract)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
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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