One-4-ALL Initiative

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-99
SponsorUniversity of Colorado, Denver

About this trial

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.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

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

Disqualifiers

None.

Trial design

Design model

Parallel

Treatments tested in this trial

  • One-4-ALL Initiative

    Behavioral

    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.

  • Control

    Behavioral

    Patients will receive standard of care.

Treatment groups

100 Participants
are divided into 2 treatment groups
Group A: One-4-ALL InitiativeActive comparator 1 intervention
Group B: ControlPlacebo comparator 1 intervention

Trial outcomes

Primary outcomes

1

Health care quality

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.

Time frame
post-intervention (12 weeks)
2

Provider satisfaction

Provider job satisfaction including level of burden and overall job satisfaction. Likert scale 1-5, higher score is best. physical and mental health

Time frame
post-intervention (12 weeks)
3

Patient satisfaction

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.

Time frame
post-intervention (12 weeks)
4

Acceptability of program tool

Patient's ability to engage and understand the program tool. Likert scale 1-5, higher score is better.

Time frame
post-intervention (12 weeks)

Secondary outcomes

Other outcomes

Sponsors and contacts

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