Parents Reading Comprehension of Their Child's Post-Operative Medicine Fact Sheets

This study has been completed.
Sponsor:
Information provided by:
State University of New York - Upstate Medical University
ClinicalTrials.gov Identifier:
NCT00639470
First received: March 12, 2008
Last updated: August 12, 2008
Last verified: August 2008
  Purpose

The objective of this study is to test legal guardians reading comprehension of their child's post-operative medication administration using three different versions of written medication information (standard fact sheets, easy-to-read fact sheets, and easy-to-read fact sheets accompanied by illustrations).


Condition Intervention
Parents
Other: easy to read fact sheets

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Open Label
Official Title: Parents Reading Comprehension of Their Child's Post-Operative Medicine Fact

Resource links provided by NLM:


Further study details as provided by State University of New York - Upstate Medical University:

Primary Outcome Measures:
  • Comprehension of the fact sheets as measured by the Cloze Readability Procedure. [ Time Frame: On the day of discharge ] [ Designated as safety issue: No ]

Enrollment: 23
Study Start Date: August 2005
Study Completion Date: August 2008
Primary Completion Date: March 2007 (Final data collection date for primary outcome measure)
Intervention Details:
    Other: easy to read fact sheets
    easy to read fact sheets with illustrations and without illustrations
    Other Name: patient education handouts
Detailed Description:

It is important for the child's welfare and comfort that the legal guardian can read and comprehend their child's pain medication information. Failure to understand the full implications of the medication may jeopardize the child's comfort level or welfare. Readability of printed education materials is a key to comprehension and supplements what healthcare providers verbally tell the parents/legal guardians. Several studies have demonstrated the benefits of using illustrations to convey intended messages. Simple line drawings appear to do well with those who have low-literacy skills.

The following hypothesis will be tested:

  • There is no difference in level of comprehension of medication administration by the legal guardians who receive standard fact sheets about medication, those who receive easy-to-read fact sheets, and those who receive easy-to-read fact sheets accompanied by illustrations.
  • There is no difference in level of comprehension of pain assessment by the legal guardians who receive standard fact sheets about assessing pain, those who receive easy-to-read fact sheets, and those who receive easy-to-read facts sheets accompanied by illustrations.
  • There is no relationship between legal guardians' satisfaction with medication education and whether they receive standard fact sheets, easy-to-read fact sheets, or those who receive easy-to read fact sheets accompanied by illustrations.
  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • be 18 years of age or older or an emancipated minor
  • ability to see, speak, and hear English
  • have a child who will be undergoing surgery
  • signed surgical consent form
  • have a child staying on hospital pediatric surgical unit after surgery until discharge
  • have a child admitted for at least one day but not more than 7 days.
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00639470

Locations
United States, New York
SUNY Upstate Medical University
Syracuse, New York, United States, 13069
Sponsors and Collaborators
State University of New York - Upstate Medical University
Investigators
Principal Investigator: Sharon Kitchie, PhD State University of New York - Upstate Medical University
  More Information

No publications provided

Responsible Party: Sharon Kitchie, PhD, APRN, BC, SUNY Upstate Medical University
ClinicalTrials.gov Identifier: NCT00639470     History of Changes
Other Study ID Numbers: IRBPHS#5229
Study First Received: March 12, 2008
Last Updated: August 12, 2008
Health Authority: United States: Institutional Review Board

Keywords provided by State University of New York - Upstate Medical University:
Patient Education Handout
Parents
Patient Education

ClinicalTrials.gov processed this record on October 19, 2014