Assessment of the Educational Experiences for Patients Newly Diagnosed With Nephrotic Syndrome

Assessment of the Educational Experience for Patients With Newly Diagnosed Nephrotic Syndrome

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT02190955

Enrollment

186

Registered

2014-07-15

Start date

2013-01-31

Completion date

2014-05-31

Last updated

2014-07-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Nephrotic Syndrome

Brief summary

The purpose of this study is to learn about patient, caregiver and healthcare worker perspectives on educating patients with newly-diagnosed Nephrotic Syndrome. All patients enrolled in the Contact Registry with Nephrotic Syndrome will be invited via email to participate in this study.

Detailed description

The survey included questions addressing the following areas: 1.) Information that is important to know when learning to manage Nephrotic Syndrome. 2.) Preferred resources for the education of patients and caregivers with newly-diagnosed Nephrotic Syndrome. 3.) The time frame required to acquire confidence in the management of Nephrotic Syndrome. 4.) Disease-specific information such as diagnosis, length of disease duration, medications used, need for kidney biopsy, dialysis and/or transplant. 5.) Demographic data such as race/ethnicity and educational background. The survey data is stored by the Rare Diseases Clinical Research Network's Data Management and Coordinating Center (DMCC) at the University of South Florida. The data is de-identified. Names or other personal health information were not collected. Upon conclusion of the study period, the data will be sent to the NEPTUNE consortium lead at the University of Michigan.

Interventions

None listed

Study design

Observational model

COHORT

Time perspective

CROSS_SECTIONAL

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

Inclusion criteria

Patient and Patient Caregiver: * 18 years or older * English literate * History of Nephrotic Syndrome \> 3 months or caregiver of a child diagnosed with Nephrotic Syndrome \> 3 months prior to enrollment * Informed Consent Healthcare Worker Inclusion Criteria: * Age \> 18 years * English literate * Provides medical care for children or adults with Nephrotic Syndrome * Informed Consent

Exclusion criteria

* Inability to provide informed consent and complete survey * Other criteria as specified by Consortium and based on the data we collect in the Contact Registry

Design outcomes

Primary

Measure	Time frame	Description
Stakeholder perspectives about educational experiences of newly-diagnosed Nephrotic Syndrome patients	1 year after the study is closed to enrollment	The outcome measure(s) will be evaluated based on the cross-sectional online questionnaire. The questionnaire is the only study procedure for this online patient contact registry protocol and will be the sole analysis tool for both the primary and secondary outcome measures.

Secondary

Measure	Time frame	Description
Perspectives of patients/families with healthcare workers regarding educational needs of newly-diagnosed Nephrotic Syndrome	1 year after the study is closed to enrollment	The outcome measure(s) will be evaluated based on the cross-sectional online questionnaire. The questionnaire is the only study procedure for this online patient contact registry protocol and will be the sole analysis tool for both the primary and secondary outcome measures.

Countries

United States

Outcome results