Human Immunodeficiency Virus Infection Clinical Trial
Official title:
Real-Life Effectiveness of the Kaletra Adherence Support Assistance (KASA) Program: A Prospective Observational Cohort Study (KASA PMOS)
The overall purpose of the study was to describe the real-life adherence, effectiveness and safety of the Kaletra Adherence Support Assistance (KASA) Program in human immunodeficiency virus (HIV)-positive patients who were receiving treatment with lopinavir / ritonavir (LPV/r; Kaletra®) in Canada.
The Kaletra Adherence Support Assistance (KASA) Program is a customized support network that
has been offered to patients treated with lopinavir / ritonavir (LPV/r; Kaletra®). KASA
offers individual counseling with an HIV experienced nurse who assists patients with various
aspects of their therapy including life-style changes, emotional stress, and adverse events.
Patients enrolled in KASA may also have access to various healthcare professionals
(dietician, social worker, psychologist, etc.) or may be offered other types of support
(transportation, exercise, etc.), which may help improve their quality of life as well as
adherence or compliance while taking LPV/r.
This was a 12-month, multi-center, Canadian Post Marketing Observational Study utilizing a
prospective single cohort design. All treatments including participation in the KASA program
were according to the decision of the treating physician and the patients and were not
affected in any way by their decision to participate in the study. Follow-up was for 12
months at an interval of every six months.
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