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. Author manuscript; available in PMC: 2016 Jan 5.
Published in final edited form as: AIDS Behav. 2014 Apr;18(4):646–660. doi: 10.1007/s10461-013-0594-x

Table 5.

Comparison of characteristics of EBIs and non-EBIs included in the PRS efficacy review (N = 65)

Characteristic 10 EBIs n (%) 55 non-EBIs n (%)
Target population
 MSM 0 (0) 1 (2)
 Drug users/IDU only 2 (20) 9 (16)
 High risk youth only 0 (0) 3 (5)
 Women only 0 (0) 9 (16)
 Men only 0 (0) 2 (4)
Race/ethnicity (not mutually exclusive)
 Majority AA 6 (60) 27 (49)
 Majority people of color (including AA, Hispanic, API, other) 5 (50) 26 (47)
 Majority white 0 (0) 5 (9)
Target groupa
 Treatment-experienced 4 (40) 27 (49)
 Treatment-naïve 1 (10) 18 (33)
 Both 5 (50) 4 (7)
Type of setting (not mutually exclusive)
 Clinic 6 (60) 34 (62)
 Community 4 (40) 1 (2)
 Other 2 (20) 34 (62)
Unit of delivery
 Individual only 6 (60) 41 (75)
 Group only 1 (10) 6 (11)
 Individual and group 3 (30) 8 (15)
 Community 0 (0) 0 (0)
Deliverer (not mutually exclusive)
 Clinic staff 6 (60) 24 (44)
 Facilitator/other 7 (70) 41 (75)
Intervention sessions
 Single-session discrete 0 (0) 2 (4)
 Multi-session discrete 3 (30) 25 (45)
 Repetitive dosing or combinationb 7 (70) 28 (51)
Outcomes measured
 Adherence only 2 (20) 19 (35)
 Viral load only 1 (10) 5 (9)
 Both 7 (70) 31 (56)
At least one statistically significant positive intervention effectc
 Yes 10 (100) 35 (64)
 No 0 (0) 20 (36)
Sample size at baseline
 Median 226 77
Follow-up time
 Median time for first follow-up (in month) 3 2
 Median time for last follow-up (in month) 9 6
Median retention
 At first “good-evidence” follow-upd 85 % 81 %
a

n = 6 non-EBIs did not target treatment naïve or experienced

b

Repetitive dosing or combination = includes interventions that had repetitive dosing and one or more discrete sessions

c

At least one statistically significant positive intervention effect on viral load or medication adherence outcomes

d

1-month post completion of intervention or 3-month post implementation of intervention