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. 2022 Sep 15;30:100997. doi: 10.1016/j.conctc.2022.100997

Table 2.

Baseline characteristics of trial participants (N = 246).

Intervention Control P-value
Number of participants 119 (48.4%) 127 (51.6%) 0.61
Mean age of participants ± Std. deviation 13.67 ± 2.43 13.98 ± 2.72 0.35
Gender of participants
Male 63 (52.9%) 60 (47.2%) 0.44
Female 56 (47.1%) 67 (52.8%)
ART Regimen at baseline
Zidovudine/Lamivudine/Nevirapine 67 (56.3%) 45 (35.4%)
Tenofovir/Lamivudine/Efavirenz 32 (26.9%) 43 (33.9%)
Tenofovir/Lamivudine/Dolutegravir 5 (4.2%) 16 (12.6%)
Abacavir/Lamivudine/Lopinavir/ritonavir 2 (1.7%) 8 (6.3%)
Zidovudine/Lamivudine/Lopinavir/ritonavir 2 (1.7%) 7 (5.5%)
Tenofovir/Lamivudine Lopinavir/ritonavir 5 (4.2%) 4 (3.1%)
Abacavir/Lamivudine/Efavirenz 5 (4.2%) 3 (2.4%)
Zidovudine/Lamivudine/Efavirenz 1 (0.8%) 1 (0.8%)
Number of participants with undetectable viral load (≤20 copies/ml) 26/119 (21.8%) 54/127 (42.5%) <0.001
Mean CD4+ count ± Std. deviation 665 ± 685 665 ± 437 0.99
Number of participants with ≥95% adherence 61/119 (51.3%) 35/127 (27.6%) <0.001

Abbreviations.

Zidovudine/Lamivudine/Lopinavir/ritonavir.

Tenofovir/Lamivudine Lopinavir/ritonavir ART Antiretroviral therapy.