Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID07314697

Arrival Time Implementation to Improve On-Time Patient Arrival for Outpatient Visits Using Behaviorally Informed Messaging

Led by University of California, Los Angeles · Updated on 2026-02-10

300000

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are investigating how changing the way appointment times are communicated to patients can improve on-time arrival for outpatient visits in primary care and related specialties. This clinical trial evaluates whether showing patients an explicit arrival time set 15 minutes before their scheduled appointment leads to earlier arrivals compared to the usual method of displaying only the appointment time and advising patients to arrive early. The study is part of UCLA Health's larger effort to enhance clinic flow and patient experience. The trial involves two groups: a control group where patients receive appointment times and instructions to arrive 15 minutes early via the MyChart patient portal and text messages, and a treatment group where patients receive an explicit arrival time displayed 15 minutes before their appointment on both platforms. The intervention is implemented at the clinic building level using cluster randomization across 37 clinic buildings. The study period lasts six months, preceded by a one-month washout period. Participants will have their arrival times recorded on the day of their appointment to measure how early they check in compared to their scheduled time. Researchers will analyze on-time arrival rates and early arrival rates, along with secondary outcomes such as appointment attendance, cancellations, patient satisfaction ratings, and clinic workflow metrics like patient room time and provider entry times. Data on participant demographics, visit types, scheduling details, and patient history will also be collected. The study runs through July 2026, with safety and operational monitoring throughout.

CONDITIONS

Brief Title

Arrival Time Implementation

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • In-person outpatient appointments with clinicians at UCLA Health during the study period
  • Appointments in Primary Care, Pediatrics, or Internal Medicine, Med Peds specialties
  • Active MyChart account status
  • Opted in to receive SMS communications from UCLA Health
  • Appointment types include Return, Well adult (physical), Well child return, New, Well adult new (physical), and Well child (new) visits
Not Eligible

You will not qualify if you...

  • Appointments at clinics not scheduled through the Patient Access Organization

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - 6 months

Participants receive appointment communications via the MyChart patient portal and Hello World text notifications that display either their appointment time (control) or their expected arrival time set 15 minutes before their scheduled appointment time (treatment). This intervention aims to improve on-time patient arrival for outpatient visits.

Outpatient visits on the day of each scheduled appointment

Trial Site Locations

Total: 1 location

1

UCLA Health Department of Medicine, Quality Office

Los Angeles, California, United States, 90095

Actively Recruiting

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How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

HEALTH_SERVICES_RESEARCH

Number of Arms

2

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