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An Automated, Tailored Information Application for Medication Health Literacy

An Automated, Tailored Information Application for Medication Health Literacy

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01304186
Enrollment
124
Registered
2011-02-25
Start date
2010-06-30
Completion date
2012-06-30
Last updated
2013-03-01

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

Conditions

Human Immunodeficiency Virus I Infection

Keywords

Health literacy, HIV, Medication Adherence, IMB Model

Brief summary

The purpose of this study is to evaluate the acceptability and efficacy of a computer-based tailored information application designed to promote health literacy in persons treated for HIV infection. The study hypothesis is that the application will be acceptable and usable for persons treated for HIV infection, and will improve their levels of adherence to antiretroviral medication treatment.

Detailed description

Health literacy is a critically important problem in improving the effectiveness of health care interventions. Patient behaviors essential to the successful treatment of HIV infection, such as high levels of medication adherence, may depend on patients understanding how to take medication, how to solve medication-related problems, and how to cope with medication side effects. An approach that has shown promise in promoting behavior change in HIV+ persons is the Information-Motivation-Behavior Skills (IMB) model. The intervention proposed in this application will implement a health literacy intervention based in part on insights about behavior change drawn from studies of this model. The purpose of the proposed research is to implement this intervention via a computer-based and automated tailored information application. Participants will first complete an automated computer-administered self interview (ACASI) that will assess medication knowledge, disease knowledge likely to be related to motivation, and problem solving skills. Results of this assessment will feed forward to an automated training application that provides individually-tailored training on these topics. This computer-based program will provide training, test understanding, and if necessary reteach and retest. It will also provide printed information for participants to take home to provide ongoing prompts. This study will comprise two phases. In the first, the program will be developed and tested with potential users to assess its usability and detect problems with the wording of materials. In the second phase, participants' health literacy and cognitive status will be evaluated, their adherence to a medication for HIV infection will be assessed using electronic monitoring, and the effects of the program on their adherence will be tested.

Interventions

The intervention comprises a computer-based application designed to provide individually-tailored information to participants in an interactive fashion.

Sponsors

National Institute of Mental Health (NIMH)
CollaboratorNIH
Nova Southeastern University
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

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

Inclusion criteria

* Aged 18 years or older * Currently treated with at least one medication for HIV infection * No change in target medication anticipated in the next two months * Able to participate in the study intervention in English

Exclusion criteria

* Psychiatric or cognitive disorder of severity sufficient to make the potential participant unable to provide informed consent. * Not able to participate in the intervention using English.

Design outcomes

Primary

MeasureTime frameDescription
Medication adherenceFour weeks after interventionMedication adherence is assessed using electronic monitoring of pill bottle openings via the Medication Event Monitoring System (MEMS) for the month before and the month after participants engage in the study intervention.

Secondary

MeasureTime frameDescription
Participant self-efficacyImmediately after completing the intervention (average time: 15 minutes) and four weeks after the intervention
MoodImmediately after completing the intervention (average time: 15 minutes) and four weeks after the intervention
Elements of the Information, Motivation, and Behavioral Skills ModelImmediately after completing the intervention (average time: 15 minutes) and four weeks after the interventionA self-report questionnaire asking participants about their knowledge, motivation, and behavioral skills with respect to HIV infection and its treatment.
Intervention acceptability and usabilityImmediately after the intervention (average time: 15 minutes) and four weeks after the interventionA questionnaire assessing elements of the Technology Acceptance Model is administered immediately after completing the intervention and four weeks after its completion.

Countries

United States

Outcome results

None listed

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