An Automated, Tailored Information Application for Medication Health Literacy
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|ClinicalTrials.gov Identifier: NCT01304186|
Recruitment Status : Completed
First Posted : February 25, 2011
Last Update Posted : March 1, 2013
|Condition or disease||Intervention/treatment|
|Human Immunodeficiency Virus I Infection||Behavioral: Tailored Information|
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||124 participants|
|Intervention Model:||Single Group Assignment|
|Masking:||None (Open Label)|
|Official Title:||An Automated, Tailored Information Application for Medication Health Literacy|
|Study Start Date :||June 2010|
|Primary Completion Date :||November 2011|
|Study Completion Date :||June 2012|
Experimental: 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.
Behavioral: Tailored Information
The intervention comprises a computer-based application designed to provide individually-tailored information to participants in an interactive fashion.
Other Name: Health literacy
- Medication adherence [ Time Frame: 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.
- Participant self-efficacy [ Time Frame: Immediately after completing the intervention (average time: 15 minutes) and four weeks after the intervention ]
- Mood [ Time Frame: Immediately after completing the intervention (average time: 15 minutes) and four weeks after the intervention ]
- Elements of the Information, Motivation, and Behavioral Skills Model [ Time Frame: 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 [ Time Frame: 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.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01304186
|United States, Florida|
|Ziff Health Clinics, Nova Southeastern University|
|Fort Lauderdale, Florida, United States, 33328|
|Principal Investigator:||Raymond L Ownby, MD, PhD||Nova Southeastern University|