Inpatient Pediatric Care

3

Review clinical trials related to Inpatient Pediatric Care. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

FIQS Dissemination and Implementation

This study is testing Family Input for Quality and Safety (FIQS), a mobile-based survey tool that allows hospitalized children's families and adolescent patients to report safety concerns in real-time by responding to a text message link on their mobile phone. The main questions it aims to answer are: 1. Does the way families are invited to use the safety reporting survey (text-only invitation versus text plus brief in-person orientation) affect how many families participate and report safety concerns? 2. Does sharing safety reports anonymously versus with patient identifiers (for example, the patient name or room number) affect how often families report concerns and how hospitals respond? 3. What barriers and supports help hospitals successfully use the reports from the survey to make safety improvements without extensive/dedicated research infrastructure? Researchers will compare different enrollment approaches and anonymous versus identified reporting across multiple children's hospitals to see which methods work best for engagement with the FIQS tool. Participants will: * Receive automated text message invitations when their child is admitted to participating hospital units * Be randomly assigned to receive either text-only invitation or an additional brief in-person orientation * Use a mobile-responsive survey to report safety concerns during their hospital stay through daily text prompts * Be randomly assigned to have their reports shared either anonymously or with identification to help hospital staff follow up * Participate during hospitalization while hospitals learn to integrate family safety reports into their quality improvement efforts

Participants needed: 21,800
Trial details
Age: 13+Biological sex: AllType: InterventionalSponsor: University of California, San FranciscoUpdated: Oct 13, 2026Locations: 8
Eligibility criteria

Family members or caregivers of patients (aged 0 to 21 years) admitted to partic... [+4]

Patients or parents/guardians who are non-English and non-Spanish speakers [+3]

Status: Recruiting

Feasibility of the Reality PAWS Program for Children in Isolation

The goal of this clinical trial is to learn if a mixed reality program, Reality PAWS, delivered on a Meta Quest 3 VR headset, is a feasible intervention for pediatric patients in isolation. It will also evaluate the safety of the program and its effect on pain, anxiety, and loneliness. The main questions the study aims to answer are: What is the feasibility of utilizing Reality PAWS MR as a substitute for in-person dog therapy for children under isolation precautions? Are patients compliant with using Reality PAWS MR? What are the interventional outcomes of Reality PAWS MR? Participants will: Wear a Meta Quest 3 VR headset with the Reality PAWS program. Interact with the program. Answer surveys regarding demographics, anxiety, pain, loneliness, sickness, perceived exertion, and immersion in the program.

Participants needed: 50
Trial details
Age: 8-21Biological sex: AllType: InterventionalSponsor: Children's Hospital ColoradoUpdated: Aug 14, 2026Locations: 2
Eligibility criteria

Children 8 to 21 years old admitted to Children's Hospital Colorado or Children'... [+2]

Traumatic brain injury, neurological disorders, neurodevelopmental issues, or ot... [+5]

Status: Recruiting

A Trial to Improve Family Clinical Note Access and Outcomes for Hospitalized Children

This study will test if giving parents access to their child's medical notes on a bedside tablet: * helps them get more involved in their care * helps identify safety concerns Parents of hospitalized children will be randomly assigned to either use the Bedside Notes tool or follow usual care. To see if this approach improves care and safety, researchers will measure: * note access * parent-reported safety concerns * overall experiences

Participants needed: 630
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University of Wisconsin, MadisonUpdated: Dec 18, 2025Locations: 3
Eligibility criteria

English and Spanish-speaking parents or guardians of children under 12 years old... [+1]

Parents of children 12 years of age and older [+3]