Trial Outcomes & Findings for Impact of LA-CEAL HALT COVID-19 Ambassador Program on Likelihood to Vaccinate (NCT NCT04930965)

NCT ID: NCT04930965

Last Updated: 2024-01-18

Results Overview

Vaccine likelihood will be measured using a single question adapted from the CEAL Common Survey (i.e., "On a scale from 1 to 7, with 1 being 'not at all likely' and 7 being 'very likely', how likely are you to get a COVID-19 vaccine in the next month?"), with "likely to vaccinate" defined as a score of 5-7.

Recruitment status

COMPLETED

Study phase

NA

Target enrollment

56 participants

Primary outcome timeframe

Month 1 follow-up

Results posted on

2024-01-18

Participant Flow

Participant milestones

Participant milestones
Measure
Intervention
Community health worker engagement: 3-4 in-person or virtual engagements (individual or group sessions) over 1 month, each engagement lasting 30 minutes to 1 hour
Usual Care
No intervention
Overall Study
STARTED
27
29
Overall Study
COMPLETED
20
24
Overall Study
NOT COMPLETED
7
5

Reasons for withdrawal

Reasons for withdrawal
Measure
Intervention
Community health worker engagement: 3-4 in-person or virtual engagements (individual or group sessions) over 1 month, each engagement lasting 30 minutes to 1 hour
Usual Care
No intervention
Overall Study
Lost to Follow-up
7
5

Baseline Characteristics

Impact of LA-CEAL HALT COVID-19 Ambassador Program on Likelihood to Vaccinate

Baseline characteristics by cohort

Baseline characteristics by cohort
Measure
Intervention
n=27 Participants
Community health worker engagement: 3-4 in-person or virtual engagements (individual or group sessions) over 1 month, each engagement lasting 30 minutes to 1 hour
Usual Care
n=29 Participants
No intervention
Total
n=56 Participants
Total of all reporting groups
Age, Continuous
41.2 years
STANDARD_DEVIATION 13.4 • n=5 Participants
44.1 years
STANDARD_DEVIATION 13.4 • n=7 Participants
42.7 years
STANDARD_DEVIATION 13.4 • n=5 Participants
Sex/Gender, Customized
Men
6 Participants
n=5 Participants
8 Participants
n=7 Participants
14 Participants
n=5 Participants
Sex/Gender, Customized
Women
21 Participants
n=5 Participants
21 Participants
n=7 Participants
42 Participants
n=5 Participants
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants
n=5 Participants
0 Participants
n=7 Participants
0 Participants
n=5 Participants
Race (NIH/OMB)
Asian
0 Participants
n=5 Participants
0 Participants
n=7 Participants
0 Participants
n=5 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants
n=5 Participants
0 Participants
n=7 Participants
0 Participants
n=5 Participants
Race (NIH/OMB)
Black or African American
24 Participants
n=5 Participants
29 Participants
n=7 Participants
53 Participants
n=5 Participants
Race (NIH/OMB)
White
0 Participants
n=5 Participants
0 Participants
n=7 Participants
0 Participants
n=5 Participants
Race (NIH/OMB)
More than one race
1 Participants
n=5 Participants
0 Participants
n=7 Participants
1 Participants
n=5 Participants
Race (NIH/OMB)
Unknown or Not Reported
2 Participants
n=5 Participants
0 Participants
n=7 Participants
2 Participants
n=5 Participants
Region of Enrollment
United States
27 participants
n=5 Participants
29 participants
n=7 Participants
56 participants
n=5 Participants

PRIMARY outcome

Timeframe: Month 1 follow-up

Vaccine likelihood will be measured using a single question adapted from the CEAL Common Survey (i.e., "On a scale from 1 to 7, with 1 being 'not at all likely' and 7 being 'very likely', how likely are you to get a COVID-19 vaccine in the next month?"), with "likely to vaccinate" defined as a score of 5-7.

Outcome measures

Outcome measures
Measure
Intervention
n=21 Participants
Community health worker engagement: 3-4 in-person or virtual engagements (individual or group sessions) over 1 month, each engagement lasting 30 minutes to 1 hour
Usual Care
n=26 Participants
No intervention
Difference in Proportion of Participants "Likely to Vaccinate" Between Study Arms at Month 1
1 Participants
3 Participants

SECONDARY outcome

Timeframe: Month 2 follow-up

Vaccine likelihood will be measured using a single question adapted from the CEAL Common Survey (i.e., "On a scale from 1 to 7, with 1 being 'not at all likely' and 7 being 'very likely', how likely are you to get a COVID-19 vaccine in the next month?"), with "likely to vaccinate" defined as a score of 5-7.

Outcome measures

Outcome measures
Measure
Intervention
n=20 Participants
Community health worker engagement: 3-4 in-person or virtual engagements (individual or group sessions) over 1 month, each engagement lasting 30 minutes to 1 hour
Usual Care
n=24 Participants
No intervention
Difference in Proportion of Participants "Likely to Vaccinate" Between Study Arms at Month 2
4 Participants
4 Participants

SECONDARY outcome

Timeframe: Month 1 follow-up

Receipt of vaccination will be measured by self-report

Outcome measures

Outcome measures
Measure
Intervention
n=21 Participants
Community health worker engagement: 3-4 in-person or virtual engagements (individual or group sessions) over 1 month, each engagement lasting 30 minutes to 1 hour
Usual Care
n=26 Participants
No intervention
Difference in Proportion of Participants Who Have Received >=1 Dose of Vaccine Between Study Arms at Month 1
1 Participants
2 Participants

SECONDARY outcome

Timeframe: Month 2 follow-up

Receipt of vaccination will be measured by self-report

Outcome measures

Outcome measures
Measure
Intervention
n=20 Participants
Community health worker engagement: 3-4 in-person or virtual engagements (individual or group sessions) over 1 month, each engagement lasting 30 minutes to 1 hour
Usual Care
n=24 Participants
No intervention
Difference in Proportion of Participants Who Have Received >=1 Dose of Vaccine Between Study Arms at Month 2
1 Participants
2 Participants

Adverse Events

Intervention

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

Usual Care

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

Serious adverse events

Adverse event data not reported

Other adverse events

Adverse event data not reported

Additional Information

Erin Peacock

Tulane University

Phone: 504-988-1075

Results disclosure agreements

  • Principal investigator is a sponsor employee
  • Publication restrictions are in place