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Social-Psychological Intervention to Improve Adherence to HAART

Effectiveness of a Social-Psychological Intervention to Improve Adherence to Antiretroviral Drug Regimens for AIDS: a Randomized Controlled Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00716040
Acronym
SPIAH-Q
Enrollment
121
Registered
2008-07-16
Start date
2008-03-31
Completion date
2008-11-30
Last updated
2008-07-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

AIDS, HIV Infections

Keywords

AIDS treatment, HAART adherence, intervention

Brief summary

All eligible patients will be invited to use electronic monitoring of medication (MEMS) during the next six months. After two months with MEMS the enrolled patients will be randomized to intervention group or to control group. The intervention group will be submitted to four social-psycho sessions with a pre-trained health professional. The control group will receive the usual care of the health service. The study will compare the rate of adherence to antiretroviral therapy between the intervention group and the control group. The duration of the study will be of six months. The analysis will be based on intention-to-treat.

Interventions

BEHAVIORALSocial-psycho intervention to improve adherence to HAART

The intervention focus on the notion of scenes and scenarios to examine and discussing the experience of taking ARV medicines. In principle, such an approach provides a tool for conscientization, action and the invention of novel group and individual repertoires that may result in individual mobilization for improving adherence to treatment and reducing his/her vulnerability.

OTHERUsual care

The control group will be submitted to the usual care of the health service

Sponsors

Fundação de Amparo à Pesquisa do Estado de São Paulo
CollaboratorOTHER_GOV
University of Sao Paulo
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients aged more than 18 years old, with detectable viral load and more than six months under HAART

Exclusion criteria

* Pregnant women * Patients participating in other trials * Patients in treatment for hepatitis and for active opportunistic infection * Patients with mental or physical condition which do not allow their attendance to the health service

Design outcomes

Primary

MeasureTime frame
Adherence to HAART24 weeks

Secondary

MeasureTime frame
Viral Load12 and 24 weeks

Countries

Brazil

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 24, 2026