An Automated, Tailored Information Application for Medication Health Literacy

Not Applicable

Completed

• Conditions: Human Immunodeficiency Virus I Infection
• Interventions: Behavioral: Tailored Information

• Registration Number: NCT01304186
• Lead Sponsor: Nova Southeastern University

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.

Study Timeline

• Study Start: 2010-06
• Study First Submitted: 2011-02-18
• Study First Submitted QC: 2011-02-23
• Study First Posted: 2011-02-25
• Primary Completion: 2011-11
• Study Completion: 2012-06
• Status Verified: 2013-02
• Last Update Submitted: 2013-02-28
• Last Update Posted: 2013-03-01

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 124

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.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
Tailored Information	Tailored Information	Participants in this arm receive the computer-based tailored information application that focuses on improving health literacy related to treatment of HIV infection.

Primary Outcome Measures

Name	Time	Method
Medication adherence	Four weeks after intervention	Medication 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 Outcome Measures

Name	Time	Method
Participant self-efficacy	Immediately after completing the intervention (average time: 15 minutes) and four weeks after the intervention
Mood	Immediately after completing the intervention (average time: 15 minutes) and four weeks after the intervention
Elements of the Information, Motivation, and Behavioral Skills Model	Immediately after completing the intervention (average time: 15 minutes) and four weeks after the intervention	A self-report questionnaire asking participants about their knowledge, motivation, and behavioral skills with respect to HIV infection and its treatment.
Intervention acceptability and usability	Immediately after the intervention (average time: 15 minutes) and four weeks after the intervention	A questionnaire assessing elements of the Technology Acceptance Model is administered immediately after completing the intervention and four weeks after its completion.

Trial Locations

Locations (1)

Ziff Health Clinics, Nova Southeastern University; 🇺🇸 Fort Lauderdale, Florida, United States