NCT06387576

Brief Summary

This is a prospective clinical trial evaluating whether a behaviorally informed intervention (pre-discharge iPad video scheduling) increases post-discharge primary care physician (PCP) appointment completion compared to the status-quo scheduling process (post-discharge via phone), with the ultimate goal of improving patient health outcomes.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
41

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Apr 2024

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

April 8, 2024

Completed
Same day until next milestone

Study Start

First participant enrolled

April 8, 2024

Completed
21 days until next milestone

First Posted

Study publicly available on registry

April 29, 2024

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 2, 2024

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

August 2, 2024

Completed
Last Updated

April 30, 2025

Status Verified

April 1, 2025

Enrollment Period

3 months

First QC Date

April 8, 2024

Last Update Submit

April 25, 2025

Conditions

Keywords

quality-improvementschedulingappointment show ratestransitions of carehospital discharge

Outcome Measures

Primary Outcomes (1)

  • Post-discharge follow-up PCP appointment completion rate within 7 days

    Binary indicator of whether the patient had a post-discharge follow-up PCP appointment

    Within 7 days of discharge

Secondary Outcomes (2)

  • Post-discharge follow-up PCP appointment completion rate within 14 days

    Within 14 days of discharge

  • Post-discharge follow-up PCP appointment scheduling rate within 7 days

    Within 7 days of discharge

Study Arms (2)

Arm 1: Status-quo post-discharge appointment scheduling process

NO INTERVENTION

Eligible, assigned participants will receive the current status-quo scheduling process for their post-discharge appointment (post-discharge via phone).

Arm 2: Pre-discharge iPad video scheduling for post-discharge appointment

EXPERIMENTAL

Eligible, assigned participants will schedule their post-discharge appointment via a video scheduling process prior to discharge.

Behavioral: Behaviorally informed pre-discharge iPad video scheduling

Interventions

The iPad video scheduling process will occur prior to patient discharge from the hospital. This intervention harnesses behavioral principles, such as commitment (patient committing to scheduled appointment), social accountability (patients feeling more accountable after scheduling their appointment via the video visit), and social support (patients feeling more supported after engaging in this conversation with a scheduler via video).

Arm 2: Pre-discharge iPad video scheduling for post-discharge appointment

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • they are discharged from a hospital room assigned to either the intervention or control condition during the intervention period
  • their discharge is ordered on a weekday (Monday-Friday)
  • their discharge is planned before 3pm
  • they have a UCLA PCP
  • they are not being discharged to a skilled nursing facility (SNF), acute rehab unit (ARU), or assisted living facility (ALF).

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

UCLA Santa Monica Medical Center

Santa Monica, California, 90404, United States

Location

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NON RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
HEALTH SERVICES RESEARCH
Intervention Model
PARALLEL
Model Details: Parallel-arm control trial
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Clinical Instructor of Medicine

Study Record Dates

First Submitted

April 8, 2024

First Posted

April 29, 2024

Study Start

April 8, 2024

Primary Completion

July 2, 2024

Study Completion

August 2, 2024

Last Updated

April 30, 2025

Record last verified: 2025-04

Data Sharing

IPD Sharing
Will not share

The investigators do not plan to make any individual participant data available.

Locations