A Study of Facilitators and Barriers to Improve Acute Kidney Injury in Children Through Mobile Health Intervention
- Conditions
- Acute Kidney Injury
- Interventions
- Other: mobile health educational tool
- Registration Number
- NCT04403633
- Lead Sponsor
- Duke University
- Brief Summary
The purpose of this study is to improve patient-centered care for acute kidney injury (AKI) in order to decrease the adverse health outcomes associated with this common condition.
- Detailed Description
There is a need to provide better patient-centered care for acute kidney injury (AKI) in order to improve the adverse health outcomes associated with this common condition. This project involves thorough evaluation of patient and provider feedback on barriers and facilitators to pediatric AKI self-management in order to develop patient-centered pediatric AKI interventions. This will be done through interviews with families of patients diagnosed with AKI and providers who take care of these patients followed by integration of the results into modification of an existing educational tool previously used in adult patients. The study will take place in three parts with the first involving interviews, the second involving tool modification and usability testing, and the third involving pilot testing of the tool's impact.
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 25
- age 1 to 18 years
- patients with diagnosis of AKI while hospitalized
- legal blindness of deafness
- cognitive impairment that limits ability to consent
- non-English speaking
- patient age greater than age 18 years, 11 months
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Receiving Educational Tool mobile health educational tool Patients in this arm will receive the educational tool after the pretest in addition to usual care.
- Primary Outcome Measures
Name Time Method Acute Kidney Injury (AKI) Knowledge Assessment score Baseline, 1 month AKI Knowledge Assessment administered as pre-test prior to intervention and post-test one month after intervention. This assessment is scored with minimum value of 0% and maximum value of 100%. A higher score is a better outcome.
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Duke University Medical Center
🇺🇸Durham, North Carolina, United States