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Evaluation of a Tailored Virtual Intervention to Empower Persons Living With HIV for Therapy Self-management

Phase 3
Completed
Conditions
HIV
Interventions
Behavioral: VIH-TAVIE
Registration Number
NCT01510340
Lead Sponsor
Centre hospitalier de l'Université de Montréal (CHUM)
Brief Summary

The purpose of this study is to evaluate the efficacy of an online virtual intervention in optimizing adherence to antiretroviral medication intake among Persons Living with HIV (PLHIV).

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
217
Inclusion Criteria
  • have to be under ART for at least six months¸
  • have internet access
Exclusion Criteria
  • be pregnant
  • active IV drug user
  • actual diagnosis of psychiatric health problem

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
VIH-TAVIEVIH-TAVIEPatients assigned to this arm must follow the four interactive computer sessions
Primary Outcome Measures
NameTimeMethod
Adherence6 months

Adherence will be evaluated through a self-administered questionnaire that was developed for and validated on the targeted population (Godin, Gagné, \& Naccache, 2003). The questionnaire comprises seven items that serve to determine how many times a person forgets to take his or her medication. The questionnaire's validity was demonstrated (sensitivity: 71 %; specificity: 72%; correct classification: 72%; odds ratio: 6.15) using immunologic (CD4 count) and virologic (viral load) parameters as validation criteria. Adherence is defined as the intake of at least 95% of prescribed tablets.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

José Côté

🇨🇦

Montréal, Quebec, Canada

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