Trial Outcomes & Findings for Program Refinements to Optimize Model Impact and Scalability Based on Evidence (NCT NCT03628287)

NCT ID: NCT03628287

Last Updated: 2024-08-30

Results Overview

TVS defined as achieving viral suppression (VL \<200 copies/mL) on the last VL test in the four months following CCP enrollment.

Recruitment status

COMPLETED

Study phase

NA

Target enrollment

960 participants

Primary outcome timeframe

Four months after CCP enrollment

Results posted on

2024-08-30

Participant Flow

Older New York City HIV surveillance registry datasets were used to determine trial eligibility for the original protocol, excluding clients who died during follow-up. 16 clients who died within 4 months of Care Coordination Program (CCP) or revised-CCP enrollment were added as eligible for trial outcome analyses. Updated surveillance and match datasets identified additional eligible individuals based on latest reported viral load at time of CCP or revised-CCP enrollment, who were also included.

Participant milestones

Participant milestones
Measure
Early-implementation
Early-implementing sites received the revised intervention starting in August 2018 (start of Period 1), with follow-up through January 2020 (end of Period 2).
Later-implementation
Later-implementing sites received the revised intervention starting in May 2019 (start of Period 2), with follow-up through January 2020 (end of Period 2).
Overall Study
STARTED
531
429
Overall Study
Period 0: No Revised Program Delivery
83
93
Overall Study
Period 1: Revised Program Delivery Only at Sites Assigned to Early Implementation
286
104
Overall Study
Period 2: Revised Program Delivery at All Sites
162
232
Overall Study
COMPLETED
531
429
Overall Study
NOT COMPLETED
0
0

Reasons for withdrawal

Withdrawal data not reported

Baseline Characteristics

Program Refinements to Optimize Model Impact and Scalability Based on Evidence

Baseline characteristics by cohort

Baseline characteristics by cohort
Measure
Early-implementation
n=531 Participants
Early-implementing sites received the revised intervention starting in August 2018 (start of Period 1), with follow-up through January 2020 (end of Period 2).
Later-implementation
n=429 Participants
Later-implementing sites received the revised intervention starting in May 2019 (start of Period 2), with follow-up through January 2020 (end of Period 2).
Total
n=960 Participants
Total of all reporting groups
Age, Customized
<25 years
24 Participants
n=99 Participants
32 Participants
n=107 Participants
56 Participants
n=206 Participants
Age, Customized
Between 25 and 44 years
194 Participants
n=99 Participants
205 Participants
n=107 Participants
399 Participants
n=206 Participants
Age, Customized
Between 45 and 54 years
148 Participants
n=99 Participants
90 Participants
n=107 Participants
238 Participants
n=206 Participants
Age, Customized
>=55 years
165 Participants
n=99 Participants
102 Participants
n=107 Participants
267 Participants
n=206 Participants
Sex/Gender, Customized
Cisgender man or boy
331 Participants
n=99 Participants
295 Participants
n=107 Participants
626 Participants
n=206 Participants
Sex/Gender, Customized
Cisgender woman or girl
185 Participants
n=99 Participants
112 Participants
n=107 Participants
297 Participants
n=206 Participants
Sex/Gender, Customized
Identified as transgender, gender nonconforming, non-binary, or not sure/questioning (TGNCNB)
15 Participants
n=99 Participants
22 Participants
n=107 Participants
37 Participants
n=206 Participants
Ethnicity (NIH/OMB)
Hispanic or Latino
183 Participants
n=99 Participants
146 Participants
n=107 Participants
329 Participants
n=206 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
347 Participants
n=99 Participants
283 Participants
n=107 Participants
630 Participants
n=206 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
1 Participants
n=99 Participants
0 Participants
n=107 Participants
1 Participants
n=206 Participants
Race/Ethnicity, Customized
American Indian or Alaska Native
0 Participants
n=99 Participants
0 Participants
n=107 Participants
0 Participants
n=206 Participants
Race/Ethnicity, Customized
Asian/Pacific Islander
0 Participants
n=99 Participants
15 Participants
n=107 Participants
15 Participants
n=206 Participants
Race/Ethnicity, Customized
Black or African American
318 Participants
n=99 Participants
230 Participants
n=107 Participants
548 Participants
n=206 Participants
Race/Ethnicity, Customized
White
24 Participants
n=99 Participants
25 Participants
n=107 Participants
49 Participants
n=206 Participants
Race/Ethnicity, Customized
More than one race/Other
5 Participants
n=99 Participants
13 Participants
n=107 Participants
18 Participants
n=206 Participants
Race/Ethnicity, Customized
Unknown or Not Reported
1 Participants
n=99 Participants
0 Participants
n=107 Participants
1 Participants
n=206 Participants
Race/Ethnicity, Customized
Hispanic or Latino
183 Participants
n=99 Participants
146 Participants
n=107 Participants
329 Participants
n=206 Participants
Region of Enrollment
United States · Bronx
244 Participants
n=99 Participants
97 Participants
n=107 Participants
341 Participants
n=206 Participants
Region of Enrollment
United States · Brooklyn
147 Participants
n=99 Participants
173 Participants
n=107 Participants
320 Participants
n=206 Participants
Region of Enrollment
United States · Manhattan
82 Participants
n=99 Participants
72 Participants
n=107 Participants
154 Participants
n=206 Participants
Region of Enrollment
United States · Queens
24 Participants
n=99 Participants
71 Participants
n=107 Participants
95 Participants
n=206 Participants
Region of Enrollment
United States · Staten Island
22 Participants
n=99 Participants
7 Participants
n=107 Participants
29 Participants
n=206 Participants
Region of Enrollment
United States · Outside NYC but within NY EMA
2 Participants
n=99 Participants
5 Participants
n=107 Participants
7 Participants
n=206 Participants
Region of Enrollment
United States · Unknown
10 Participants
n=99 Participants
4 Participants
n=107 Participants
14 Participants
n=206 Participants
Primary Language
English
437 Participants
n=99 Participants
304 Participants
n=107 Participants
741 Participants
n=206 Participants
Primary Language
Other
94 Participants
n=99 Participants
124 Participants
n=107 Participants
218 Participants
n=206 Participants
Primary Language
Unknown
0 Participants
n=99 Participants
1 Participants
n=107 Participants
1 Participants
n=206 Participants
Country of Birth
US/US territory
433 Participants
n=99 Participants
237 Participants
n=107 Participants
670 Participants
n=206 Participants
Country of Birth
Other country
98 Participants
n=99 Participants
192 Participants
n=107 Participants
290 Participants
n=206 Participants
Transmission Risk
Men who have sex with men (MSM)
149 Participants
n=99 Participants
172 Participants
n=107 Participants
321 Participants
n=206 Participants
Transmission Risk
Injection drug users (IDU)
32 Participants
n=99 Participants
18 Participants
n=107 Participants
50 Participants
n=206 Participants
Transmission Risk
MSM/IDU
3 Participants
n=99 Participants
5 Participants
n=107 Participants
8 Participants
n=206 Participants
Transmission Risk
Heterosexual
298 Participants
n=99 Participants
207 Participants
n=107 Participants
505 Participants
n=206 Participants
Transmission Risk
Perinatal
32 Participants
n=99 Participants
20 Participants
n=107 Participants
52 Participants
n=206 Participants
Transmission Risk
Other/Unknown
17 Participants
n=99 Participants
7 Participants
n=107 Participants
24 Participants
n=206 Participants
Housing Status
Stably housed
378 Participants
n=99 Participants
351 Participants
n=107 Participants
729 Participants
n=206 Participants
Housing Status
Unstably housed or unhoused
153 Participants
n=99 Participants
78 Participants
n=107 Participants
231 Participants
n=206 Participants
Incarceration History
Never
352 Participants
n=99 Participants
355 Participants
n=107 Participants
707 Participants
n=206 Participants
Incarceration History
Last 12 months
25 Participants
n=99 Participants
10 Participants
n=107 Participants
35 Participants
n=206 Participants
Incarceration History
>12 months ago
147 Participants
n=99 Participants
61 Participants
n=107 Participants
208 Participants
n=206 Participants
Incarceration History
Unknown
7 Participants
n=99 Participants
3 Participants
n=107 Participants
10 Participants
n=206 Participants
Sexual Orientation
Gay or Lesbian
125 Participants
n=99 Participants
141 Participants
n=107 Participants
266 Participants
n=206 Participants
Sexual Orientation
Straight or Heterosexual
339 Participants
n=99 Participants
240 Participants
n=107 Participants
579 Participants
n=206 Participants
Sexual Orientation
Bisexual
33 Participants
n=99 Participants
31 Participants
n=107 Participants
64 Participants
n=206 Participants
Sexual Orientation
Other/Unknown
34 Participants
n=99 Participants
17 Participants
n=107 Participants
51 Participants
n=206 Participants
Mental Health Diagnosis/Condition
Yes
286 Participants
n=99 Participants
147 Participants
n=107 Participants
433 Participants
n=206 Participants
Mental Health Diagnosis/Condition
No
222 Participants
n=99 Participants
259 Participants
n=107 Participants
481 Participants
n=206 Participants
Mental Health Diagnosis/Condition
Unknown
23 Participants
n=99 Participants
23 Participants
n=107 Participants
46 Participants
n=206 Participants
Recent Hard Drug Use
Yes
113 Participants
n=99 Participants
70 Participants
n=107 Participants
183 Participants
n=206 Participants
Recent Hard Drug Use
No
407 Participants
n=99 Participants
354 Participants
n=107 Participants
761 Participants
n=206 Participants
Recent Hard Drug Use
Unknown
11 Participants
n=99 Participants
5 Participants
n=107 Participants
16 Participants
n=206 Participants
Lifetime Hard Drug Use
Yes
178 Participants
n=99 Participants
116 Participants
n=107 Participants
294 Participants
n=206 Participants
Lifetime Hard Drug Use
No
343 Participants
n=99 Participants
309 Participants
n=107 Participants
652 Participants
n=206 Participants
Lifetime Hard Drug Use
Unknown
10 Participants
n=99 Participants
4 Participants
n=107 Participants
14 Participants
n=206 Participants
Insurance Status
Insured
476 Participants
n=99 Participants
299 Participants
n=107 Participants
775 Participants
n=206 Participants
Insurance Status
Uninsured
55 Participants
n=99 Participants
130 Participants
n=107 Participants
185 Participants
n=206 Participants
Employment Status
Any paid employment
76 Participants
n=99 Participants
134 Participants
n=107 Participants
210 Participants
n=206 Participants
Employment Status
No paid employment
451 Participants
n=99 Participants
283 Participants
n=107 Participants
734 Participants
n=206 Participants
Employment Status
Unknown
4 Participants
n=99 Participants
12 Participants
n=107 Participants
16 Participants
n=206 Participants
Federal Poverty Level (FPL)
<100% of FPL
456 Participants
n=99 Participants
324 Participants
n=107 Participants
780 Participants
n=206 Participants
Federal Poverty Level (FPL)
100%-200% of FPL
54 Participants
n=99 Participants
78 Participants
n=107 Participants
132 Participants
n=206 Participants
Federal Poverty Level (FPL)
>200% of FPL
21 Participants
n=99 Participants
27 Participants
n=107 Participants
48 Participants
n=206 Participants
Educational Level
≤High school/GED or equivalent
398 Participants
n=99 Participants
302 Participants
n=107 Participants
700 Participants
n=206 Participants
Educational Level
>High school/GED
130 Participants
n=99 Participants
124 Participants
n=107 Participants
254 Participants
n=206 Participants
Educational Level
Unknown
3 Participants
n=99 Participants
3 Participants
n=107 Participants
6 Participants
n=206 Participants
Time Since Diagnosis
≤1 year pre-enrollment
51 Participants
n=99 Participants
103 Participants
n=107 Participants
154 Participants
n=206 Participants
Time Since Diagnosis
>1 to 10 years pre-enrollment
111 Participants
n=99 Participants
110 Participants
n=107 Participants
221 Participants
n=206 Participants
Time Since Diagnosis
>10 to 20 years pre-enrollment
199 Participants
n=99 Participants
114 Participants
n=107 Participants
313 Participants
n=206 Participants
Time Since Diagnosis
>20 years pre-enrollment
170 Participants
n=99 Participants
102 Participants
n=107 Participants
272 Participants
n=206 Participants
Antiretroviral Therapy (ART) Status
On ART
479 Participants
n=99 Participants
381 Participants
n=107 Participants
860 Participants
n=206 Participants
Antiretroviral Therapy (ART) Status
Not on ART
52 Participants
n=99 Participants
48 Participants
n=107 Participants
100 Participants
n=206 Participants
Viral Load
200-1,499
101 Participants
n=99 Participants
80 Participants
n=107 Participants
181 Participants
n=206 Participants
Viral Load
1,500-9,999
85 Participants
n=99 Participants
74 Participants
n=107 Participants
159 Participants
n=206 Participants
Viral Load
10,000+
339 Participants
n=99 Participants
264 Participants
n=107 Participants
603 Participants
n=206 Participants
Viral Load
No viral load at enrollment
6 Participants
n=99 Participants
11 Participants
n=107 Participants
17 Participants
n=206 Participants
Cluster of differentiation 4 (CD4) Count
<200
234 Participants
n=99 Participants
188 Participants
n=107 Participants
422 Participants
n=206 Participants
Cluster of differentiation 4 (CD4) Count
200-499
196 Participants
n=99 Participants
156 Participants
n=107 Participants
352 Participants
n=206 Participants
Cluster of differentiation 4 (CD4) Count
500+
94 Participants
n=99 Participants
76 Participants
n=107 Participants
170 Participants
n=206 Participants
Cluster of differentiation 4 (CD4) Count
No CD4 at enrollment
7 Participants
n=99 Participants
9 Participants
n=107 Participants
16 Participants
n=206 Participants

PRIMARY outcome

Timeframe: Four months after CCP enrollment

Population: The final analysis used an intention-to-treat design and included all 960 participants recruited at baseline. No participants were lost to follow-up.

TVS defined as achieving viral suppression (VL \<200 copies/mL) on the last VL test in the four months following CCP enrollment.

Outcome measures

Outcome measures
Measure
Early-implementation
n=531 Participants
Early-implementing sites received the revised intervention starting in August 2018 (start of Period 1), with follow-up through January 2020 (end of Period 2).
Later-implementation
n=429 Participants
Later-implementing sites received the revised intervention starting in May 2019 (start of Period 2), with follow-up through January 2020 (end of Period 2).
Timely Viral Suppression (TVS)
Achieved TVS (suppressed within four months)
254 Participants
261 Participants
Timely Viral Suppression (TVS)
Did not achieve TVS (unsuppressed)
277 Participants
168 Participants

Adverse Events

Early-implementation

Serious events: 0 serious events
Other events: 0 other events
Deaths: 9 deaths

Later-implementation

Serious events: 0 serious events
Other events: 0 other events
Deaths: 7 deaths

Serious adverse events

Adverse event data not reported

Other adverse events

Adverse event data not reported

Additional Information

Denis Nash, PhD

City University of New York, School of Public Health

Phone: 347-331-6554

Results disclosure agreements

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