Effectiveness of Using Educational Modules Via Bedside Tablet in Newly Diagnosed Type 1 Diabetes
Status: | Recruiting |
---|---|
Conditions: | Diabetes, Diabetes |
Therapuetic Areas: | Endocrinology |
Healthy: | No |
Age Range: | Any - 21 |
Updated: | 5/25/2018 |
Start Date: | April 17, 2017 |
End Date: | June 2020 |
Contact: | Susan Mathus, BSN |
Email: | susan.mathus@hackensackmeridian.org |
Phone: | 551-996-8178 |
This is a prospective, randomized trial to evaluate the effectiveness of using educational
modules accessed through a bedside tablet in patients newly diagnosed with Type 1 Diabetes as
an adjunct to *standard Children's Hospital- Molly Center diabetes education in comparison to
*standard Children's Hospital- Molly Center diabetes education. (standard diabetes education
consists of paper based reading material and nursing education).
modules accessed through a bedside tablet in patients newly diagnosed with Type 1 Diabetes as
an adjunct to *standard Children's Hospital- Molly Center diabetes education in comparison to
*standard Children's Hospital- Molly Center diabetes education. (standard diabetes education
consists of paper based reading material and nursing education).
Type I diabetes is one of the most common diseases of childhood and its incidence has been
increasing worldwide. By age 18, 1 in 300 children will be affected by Type 1 Diabetes1. Not
only are children diagnosed with diabetes met with significant morbidity due to their
disease, but they are also expected to be active participants in daily often complicated
treatment regimens. As children with Type 1 diabetes grow older and eventually spend time
away from their parents or caregivers, they are forced to manage their own care. Over the
last several years, health systems in the United States have become more patient-centered and
have focused on autonomy and patient preference. With the advent of technology that makes
self-directed education possible, this patient-centered approach needs to be applied to
children diagnosed with Type I diabetes.
When clinicians are at the center of educating patients with diabetes, they often communicate
more directly with parents, who then use the information they receive to manage their child's
care. This model, however, does not account for the fact that children with diabetes will one
day need to manage their own care and that patients who are active participants and who
understand their disease process will be more likely to cooperate with treatment regimens and
lifestyle interventions. It is often difficult for any patient, child or adult, to process
educational information provided verbally in a physician's office, especially immediately
after they have been diagnosed with a life-long disease. Educational tools therefore need to
focus on incorporating methods that best serve the patients being educated.
Since individuals learn in different ways and at different paces, interactive educational
tools can help patients and their families learn in a way that can be individualized and
private and can also be fun and creative. As our patients are growing up surrounded by
technology, the use of this technology for education might provide a sense of normalcy to
children and teenagers already overwhelmed by processes that are often difficult for them to
identify with or understand. We hope that patients and families who are given the opportunity
to learn independently will become better equipped to manage self-care and will develop a
sense of involvement in their treatment. Interactive tools will also help patients and
families become more actively engaged in understanding their disease process and can help
them to become more active participants in their care.
increasing worldwide. By age 18, 1 in 300 children will be affected by Type 1 Diabetes1. Not
only are children diagnosed with diabetes met with significant morbidity due to their
disease, but they are also expected to be active participants in daily often complicated
treatment regimens. As children with Type 1 diabetes grow older and eventually spend time
away from their parents or caregivers, they are forced to manage their own care. Over the
last several years, health systems in the United States have become more patient-centered and
have focused on autonomy and patient preference. With the advent of technology that makes
self-directed education possible, this patient-centered approach needs to be applied to
children diagnosed with Type I diabetes.
When clinicians are at the center of educating patients with diabetes, they often communicate
more directly with parents, who then use the information they receive to manage their child's
care. This model, however, does not account for the fact that children with diabetes will one
day need to manage their own care and that patients who are active participants and who
understand their disease process will be more likely to cooperate with treatment regimens and
lifestyle interventions. It is often difficult for any patient, child or adult, to process
educational information provided verbally in a physician's office, especially immediately
after they have been diagnosed with a life-long disease. Educational tools therefore need to
focus on incorporating methods that best serve the patients being educated.
Since individuals learn in different ways and at different paces, interactive educational
tools can help patients and their families learn in a way that can be individualized and
private and can also be fun and creative. As our patients are growing up surrounded by
technology, the use of this technology for education might provide a sense of normalcy to
children and teenagers already overwhelmed by processes that are often difficult for them to
identify with or understand. We hope that patients and families who are given the opportunity
to learn independently will become better equipped to manage self-care and will develop a
sense of involvement in their treatment. Interactive tools will also help patients and
families become more actively engaged in understanding their disease process and can help
them to become more active participants in their care.
Inclusion Criteria:
- New diagnosed Type 1 Diabetes admitted to the Joseph M. Sanzari Children's Hospital
- Patient/Caretaker/Family willing to complete questionnaires
Exclusion Criteria:
- Patients with previous history of Diabetes
- Patients with no plans to follow up at The Joseph M. Sanzari Children's Hospital -
Molly's Center for Children with Diabetes and Endocrine Disorders after hospital
discharge
- Non English speaking patients/family/caretaker
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