Actively Recruiting
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
Eligibility Criteria
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
You will not qualify if you...
- Appointments at clinics not scheduled through the Patient Access Organization
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
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
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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