NCT00127543

Brief Summary

This study is being done to see if education about medicines directed toward children will improve their knowledge. The investigators also want to know if this knowledge lasts over time. Right now there are few medication instructional cards that are appropriate for children. Most of the medication cards provide information for adults. Some studies have shown that by teaching children directly, the children may take medicine at the right time for the right reason, have fewer side effects and know more about their medicine. The purpose of this research study is to see if education about medication helps children learn more about their medicine and if this knowledge lasts.

Trial Health

30
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Timeline
Completed

Started Aug 2005

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
withdrawn

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

August 1, 2005

Completed
4 days until next milestone

First Submitted

Initial submission to the registry

August 5, 2005

Completed
3 days until next milestone

First Posted

Study publicly available on registry

August 8, 2005

Completed
8 months until next milestone

Study Completion

Last participant's last visit for all outcomes

April 1, 2006

Completed
Last Updated

January 5, 2021

Status Verified

December 1, 2020

First QC Date

August 5, 2005

Last Update Submit

December 30, 2020

Conditions

Keywords

Medication EducationPediatric

Outcome Measures

Primary Outcomes (3)

  • Develop medication cards appropriate for children

  • Develop a post-test to determine the effectiveness

  • Obtain data to support teaching children about medication

Secondary Outcomes (1)

  • Assess the clinical implications of this research

Interventions

Eligibility Criteria

Age7 Years - 11 Years
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17)

You may qualify if:

  • Between the ages of 7 - 11 years
  • Currently receiving disease management primarily coordinated through the Hematology/Oncology section
  • Receiving a medication identified as a variable for this study
  • Are able to assent and have a parent/guardian who is willing to consent to study participation
  • Suffer no apparent developmental difficulty that would prevent or make study participation difficult

You may not qualify if:

  • Individuals who cannot read or write English
  • Individuals who are known to be non-compliant with medication routine and/or adhering to follow-up visits.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Childrens Mercy Hospitals and Clinics

Kansas City, Missouri, 64108, United States

Location

MeSH Terms

Conditions

Hemophilia AAnemia, Sickle CellNeoplasmsBlood Coagulation Disorders

Condition Hierarchy (Ancestors)

Blood Coagulation Disorders, InheritedHematologic DiseasesHemic and Lymphatic DiseasesCoagulation Protein DisordersHemorrhagic DisordersGenetic Diseases, InbornCongenital, Hereditary, and Neonatal Diseases and AbnormalitiesAnemia, Hemolytic, CongenitalAnemia, HemolyticAnemiaHemoglobinopathies

Study Officials

  • Heather E Curry, RN, MSN

    Childrens Mercy Hospitals and Clinics

    PRINCIPAL INVESTIGATOR
0

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NON RANDOMIZED
Masking
NONE
Purpose
OTHER
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

August 5, 2005

First Posted

August 8, 2005

Study Start

August 1, 2005

Study Completion

April 1, 2006

Last Updated

January 5, 2021

Record last verified: 2020-12

Locations