Trial Outcomes & Findings for The Oakland Men's Health Disparities Study (NCT NCT03481270)
NCT ID: NCT03481270
Last Updated: 2019-10-25
Results Overview
Take-up of preventative services was scored as either zero (did not utilize any post-consultation services) or 1 (utilized at least 1 post-consultation service). Four non-incentivized post-consultation preventive services were offered (for BMI, blood pressure, cholesterol, and/or diabetes); the subject had the opportunity to select service(s) after meeting with their assigned doctor.
COMPLETED
NA
1374 participants
1 day
2019-10-25
Participant Flow
We recruited 1374 black men in barbershops and flea markets to take the baseline survey. The subjects were given a coupon which allowed them entrance to the clinic.
1374 participants were recruited and completed the baseline survey prior to coming to the clinic. 667 filled out the baseline survey but did not come to the clinic and were not randomized. 70 additional participants were excluded from participation and were not randomized.
Participant milestones
| Measure |
Discordant
Subject is not randomized to a concordant provider.
Concordant: The black male subject is seen by a non-black male doctor.
|
Concordant
Subject is randomized to a concordant provider.
Concordant: The black male subject is seen by a black male doctor.
|
|---|---|---|
|
Overall Study
STARTED
|
324
|
313
|
|
Overall Study
COMPLETED
|
324
|
313
|
|
Overall Study
NOT COMPLETED
|
0
|
0
|
Reasons for withdrawal
Withdrawal data not reported
Baseline Characteristics
The Oakland Men's Health Disparities Study
Baseline characteristics by cohort
| Measure |
Discordant
n=324 Participants
Does not receive the concordant provider.
Concordant: We will be randomizing across providers - we are particularly interested in racial concordance.
|
Concordant
n=313 Participants
The intervention is that the subject receives the concordant provider.
Concordant: We will be randomizing across providers - we are particularly interested in racial concordance.
|
Total
n=637 Participants
Total of all reporting groups
|
|---|---|---|---|
|
Age, Continuous
|
43.4 years
STANDARD_DEVIATION 16.3 • n=93 Participants
|
42.6 years
STANDARD_DEVIATION 17.1 • n=4 Participants
|
43.0 years
STANDARD_DEVIATION 16.7 • n=27 Participants
|
|
Sex: Female, Male
Female
|
0 Participants
n=93 Participants
|
0 Participants
n=4 Participants
|
0 Participants
n=27 Participants
|
|
Sex: Female, Male
Male
|
324 Participants
n=93 Participants
|
313 Participants
n=4 Participants
|
637 Participants
n=27 Participants
|
|
Race (NIH/OMB)
American Indian or Alaska Native
|
0 Participants
n=93 Participants
|
0 Participants
n=4 Participants
|
0 Participants
n=27 Participants
|
|
Race (NIH/OMB)
Asian
|
0 Participants
n=93 Participants
|
0 Participants
n=4 Participants
|
0 Participants
n=27 Participants
|
|
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
|
0 Participants
n=93 Participants
|
0 Participants
n=4 Participants
|
0 Participants
n=27 Participants
|
|
Race (NIH/OMB)
Black or African American
|
324 Participants
n=93 Participants
|
313 Participants
n=4 Participants
|
637 Participants
n=27 Participants
|
|
Race (NIH/OMB)
White
|
0 Participants
n=93 Participants
|
0 Participants
n=4 Participants
|
0 Participants
n=27 Participants
|
|
Race (NIH/OMB)
More than one race
|
0 Participants
n=93 Participants
|
0 Participants
n=4 Participants
|
0 Participants
n=27 Participants
|
|
Race (NIH/OMB)
Unknown or Not Reported
|
0 Participants
n=93 Participants
|
0 Participants
n=4 Participants
|
0 Participants
n=27 Participants
|
|
Average education level
|
.62 score on a scale
STANDARD_DEVIATION .49 • n=93 Participants
|
.64 score on a scale
STANDARD_DEVIATION .48 • n=4 Participants
|
.63 score on a scale
STANDARD_DEVIATION .48 • n=27 Participants
|
PRIMARY outcome
Timeframe: 1 dayTake-up of preventative services was scored as either zero (did not utilize any post-consultation services) or 1 (utilized at least 1 post-consultation service). Four non-incentivized post-consultation preventive services were offered (for BMI, blood pressure, cholesterol, and/or diabetes); the subject had the opportunity to select service(s) after meeting with their assigned doctor.
Outcome measures
| Measure |
Discordant
n=324 Participants
Subject is not randomized to a concordant provider.
Concordant: The black male subject is seen by a non-black male doctor.
|
Concordant
n=313 Participants
Subject is randomized to a concordant provider.
Concordant: The black male subject is seen by a black male doctor.
|
|---|---|---|
|
Average Take-up of Preventive Services (Post-consultation)
|
0.52 score on a scale
Standard Deviation .36
|
.71 score on a scale
Standard Deviation .36
|
Adverse Events
Discordant
Concordant
Serious adverse events
Adverse event data not reported
Other adverse events
Adverse event data not reported
Additional Information
Marcella Alsan, Associate Professor of Medicine
Stanford University
Results disclosure agreements
- Principal investigator is a sponsor employee
- Publication restrictions are in place