Decreasing Medication Errors by Caregivers Using a Health Literacy Intervention
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|ClinicalTrials.gov Identifier: NCT01294501|
Recruitment Status : Terminated (PI left the institution)
First Posted : February 11, 2011
Last Update Posted : April 24, 2015
|Condition or disease||Intervention/treatment|
|Medication Administration Medication Errors||Other: Medication administration educational module|
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||132 participants|
|Intervention Model:||Single Group Assignment|
|Primary Purpose:||Health Services Research|
|Official Title:||Decreasing Medication Errors by Caregivers Using a Health Literacy Intervention|
|Study Start Date :||February 2011|
|Primary Completion Date :||January 2013|
|Study Completion Date :||January 2013|
Experimental: Fever assessment and management
Medication administration educational module for low literacy subjects on how to administer common medications appropriately and safely.
Other: Medication administration educational module
The Research Assistant (RA) will enter the subject's language (English or Spanish), the type of medicine (tablet/capsule, liquid, or ointment) from the antibiotic prescription, and the frequency (once a day, twice a day, three times a day, four times a day) from the antibiotic prescription into the web-based educational module on medication administration so that a tailored module will be setup for the subject. The subject will then view the educational interactive module. After the subject is done with the module, the RA will administer a verbal post-test. The post-test will include questions on medication administration as well as questions on fever assessment and management.
Other Name: Health Literacy Intervention
- Score on the telephone interview post-test [ Time Frame: 48-72 hours post Emergency Department visit ]Subject scores will be dichotomized in the follow way: anything less than 100% will be considered incorrect, a score of 100% will be considered correct.
- Prevalence of perfect performance on each element of the questionnaire [ Time Frame: 48-72 hours post Emergency Department visit ]Each answer on the telephone interview post-test will be dichotomized into a correct/incorrect answer.
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): NCT01294501
|United States, New York|
|Columbia University Medical Center|
|New York, New York, United States, 10032|
|Principal Investigator:||Anupama Subramony, MD, MBA||Columbia University|