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Theory- and evidence-based intervention to improve adherence to antiretroviral therapy among human immunodeficiency virus (HIV)-infected patients: the AIMS study

Not Applicable
Completed
Conditions
Human immunodeficiency virus (HIV)
Infections and Infestations
Registration Number
ISRCTN97730834
Lead Sponsor
Academic Medical Centre (AMC) (Netherlands)
Brief Summary

2005 Results article in https://www.ncbi.nlm.nih.gov/pubmed/15989434 results of pilot study results 2010 Results article in https://pubmed.ncbi.nlm.nih.gov/20658830/ results (added 22/10/2021)

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
All
Target Recruitment
133
Inclusion Criteria

1. HIV-1 positive, using highly active anti-retroviral therapy (HAART)
2. Treatment experience for at least 6 months, with a maximum of 5 years
3. Sufficient knowledge of the English or Dutch language (verbal and in writing)
4. No current psychiatric, drug or alcohol problems
5. More or less stable housing
6. Able to give informed consent.

Exclusion Criteria

Does not comply with the above inclusion criteria

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
<br> 1. The primary purpose of the proposed study is to investigate whether or not adherence to HAART can be significantly increased by HIV-nurses using the AIM-Strategy, and whether this is sustained over time<br> 2. Whether or not these improvements result in a decrease of plasma and intracellular HIV-RNA<br>
Secondary Outcome Measures
NameTimeMethod
<br> 1. Furthermore, a questionnaire will be used to see which cognitive variables of the patients are related to (non) adherence and to evaluate whether or not the intervention successfully changes those cognitive variables that cause non-adherence<br> 2. Finally, a process evaluation will be conducted among patients, HIV-nurses and physicians to investigate the advantages (e.g., insight in adherence, detection of treatment problems, improved communication) and disadvantages (e.g. duration intervention sessions, user-friendliness of equipment) of the use of AIMS versus providing standard care<br>
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