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One-4-ALL Initiative

Transforming Healthcare in Post-Pandemic Recovery: Innovation in Process & Technology to Increase Patient Throughput While Reducing Clinician Burden and Addressing Health Disparities (One-4-ALL Initiative)

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05454969
Enrollment
100
Registered
2022-07-12
Start date
2023-09-01
Completion date
2025-12-30
Last updated
2024-10-01

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

Conditions

Burden, Caregiver, Health Care Utilization, Literacy

Brief summary

This study aims to improve health outcomes of individuals and populations, enhance the patient experience, reduce the per capita cost of care, and ensure the well-being of our healthcare providers (quadruple aim). These goals are increasingly difficult to achieve, given the challenges of changes to workflow, staffing shortages, and increased costs brought on by the COVID-19 pandemic. Further, the pandemic brought to light the critical need to transform healthcare access for our racially and culturally minoritized and low-income families that have long been victims of health disparities, specifically with poorer health outcomes.

Detailed description

The overall objective is to successfully implement a patient app that will be used by families to 1) increase throughput for all patients, including minoritized, low-income, and low health literacy patients, and 2) reduce administrative burdens on providers. To evaluate this hypothesis, the following specific aims will be examined: Aim 1: Document modifiable factors that negatively and positively impact providers' ability to provide high-quality patient care in a post-pandemic healthcare system while addressing health disparities through implementation science. Aim 2: Create a boarding pass' experience for providers and patients using technology (app) which allows patients and their families to fully prepare for their clinical visits and bridge care between home, primary care providers, and specialty care. Aim 3: Investigate multilevel contextual factors related to app implementation, to inform future strategies to promote scalability and sustainability of app in all specialties.

Interventions

BEHAVIORALOne-4-ALL Initiative

We can successfully implement a patient app that will be used by families to 1) increase throughput for all patients, including minoritized, low-income, and low health literacy patients, and 2) reduce administrative burdens on providers.

BEHAVIORALControl

Patients will receive standard of care.

Sponsors

University of Colorado, Denver
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Intervention model description

This is a randomized controlled trial to examine pre-post differences between individuals that use the app versus the standard of care.

Eligibility

Sex/Gender
ALL
Age
18 Years to 99 Years
Healthy volunteers
Yes

Inclusion criteria

* All guardians of patients and the providers (surgeons, doctors, nurses, etc) that serve these patients.

Exclusion criteria

* None.

Design outcomes

Primary

MeasureTime frameDescription
Health care qualitypost-intervention (12 weeks)Health care quality will be assessed using six domains; safety, effective, patient-centered, timely, efficient, and equitable. Likert scale 1-5, higher score is best.
Provider satisfactionpost-intervention (12 weeks)Provider job satisfaction including level of burden and overall job satisfaction. Likert scale 1-5, higher score is best. physical and mental health
Patient satisfactionpost-intervention (12 weeks)Patient's satisfaction of the program tool. Likert scale 1-5, higher score is best. literacy of the patient & their family, patient & family anxiety pre-surgery.
Acceptability of program toolpost-intervention (12 weeks)Patient's ability to engage and understand the program tool. Likert scale 1-5, higher score is better.

Countries

United States

Contacts

Primary ContactJill Landsbaugh Kaar, PhD
jill.kaar@cuanschutz.edu17207773571

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026