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Sponsored by: |
National Taiwan University Hospital |
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Information provided by: | National Taiwan University Hospital |
ClinicalTrials.gov Identifier: | NCT00677131 |
The primary purpose of this study is to evaluate the patient education efficacy of the pharmacists in National Taiwan University Hospital. We randomize patient family into one of the following three groups:
Then we will evaluate the difference on patient knowledge of reconstitution, storage, and administration of oral antibiotic suspension from powder dosage form between these three groups.
Condition | Intervention |
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Infection |
Other: Reading the package insert of the drug Other: Reading the education information provided by the Pharmacy of NTUH Other: Oral education provided by the pharmacist |
Study Type: | Interventional |
Study Design: | Health Services Research, Randomized, Open Label, Active Control, Parallel Assignment, Efficacy Study |
Official Title: | Study of the Evaluation of Patient Education Efficacy: Reconstitution, Storage, and Administration of Oral Antibiotic Suspension From Powder Dosage Form at Pharmacy of National Taiwan University Hospital |
Estimated Enrollment: | 500 |
Study Start Date: | May 2008 |
Estimated Study Completion Date: | December 2009 |
Estimated Primary Completion Date: | December 2009 (Final data collection date for primary outcome measure) |
Arms | Assigned Interventions |
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1: Active Comparator
To read the package insert of the drug
|
Other: Reading the package insert of the drug
package insert of the drug
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2: Active Comparator
To read the education information provided by the Pharmacy of NTUH
|
Other: Reading the education information provided by the Pharmacy of NTUH
education information
|
3: Active Comparator
Oral education provided by the pharmacist
|
Other: Oral education provided by the pharmacist
Oral education provided by the pharmacist
|
The primary purpose of this study is to evaluate the patient education efficacy of the pharmacists in National Taiwan University Hospital. We designed twelve questions about reconstitution, storage, and administration of oral antibiotic suspension from powder dosage form in a questionnaire. We will recruit pediatric patients who are prescribed one of the two oral antibiotics powder for suspension, Augmentin and Zithromax. We will randomize the family of these patients into one of the following three groups:
Then we will ask them the twelve questions in the questionnaire and record their answer. Eventually, we will be able to compare the number of the correct answer, and to evaluate the difference on patient knowledge of reconstitution, storage, and administration of oral antibiotic suspension from powder dosage form between these three groups.
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
Exclusion Criteria:
Contact: Li J Shen, doctor | 886-2-2312-3456 ext 8411 | ljshen@ntu.edu.tw |
Taiwan | |
National Taiwan University Hospital | |
Taipei, Taiwan, 100 |
Principal Investigator: | Li J Shen, doctor | National Taiwan University Hospital |
Responsible Party: | National Taiwan University Hospital ( Li-Jiuan Shen ) |
Study ID Numbers: | 200803049R |
Study First Received: | May 8, 2008 |
Last Updated: | May 12, 2008 |
ClinicalTrials.gov Identifier: | NCT00677131 |
Health Authority: | Taiwan: Department of Health |
pediatrics antibiotics patient education |
Infection |