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OpenTrials
Completed

NCT Number: NCT06767423

Comparing the Effectiveness of Different Appointment Reminder Methods

Penn Medicine is continually trying to optimize operations and decrease number of patients who do not show up for their appointments. This has included new changes to text message reminders, implemented as usual care. At a baseline, less than 75% of scheduled outpatient appointments are actually completed. This results in longer wait times and decreased access for patients and operational inefficiencies. The goal of the project is to test whether supplementing standard text message appointment reminders with targeted outreach using an automated phone call to patients with increased risk of not showing up for their appointment (>15% per Epic's Risk of Patient No-Show Model) reduces no show rate (the study's primary outcome) and increases patient appointment completion rate (% of appointments that were completed during scheduled appointment time, a secondary outcome). Participants will be randomized in a 1:1 ratio to receive either the standard text message or standard text message plus the automated caller. Eligible patients have already consented to receiving text message reminders from Penn Medicine and must have an in-person appointment scheduled during the study period. The Access Optimization Group at Penn will be monitoring the randomization and outcomes reporting of whether a patient confirmed, cancelled, or no showed at the scheduled appointment. All eligible outpatient appointments over a two week period will be included in this operational evaluation. The Access Optimization Group will then make a decision on which approach to implement as usual care based on the results of this operational evaluation.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Penn Medicine

Philadelphia, Pennsylvania, 19104, United States

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • in-person appointments
  • English or Spanish speakers
  • 18 years old or older

Treatment and study plan

Text Message + Automated Caller (Intervention)

Behavioral

Standard text message appointment reminders to English and Spanish-speaking patients. Text reminders will go out 3-weeks, 3 days, and 24 hours before the appointment. If patient has not confirmed their appointment after the 3-week and 3-day reminders they will receive an automated caller.

Primary outcomes

  1. No Show Rate

    Time frame: Through study completion, on average of 3 weeks

    Proportion of initially scheduled appointments in which the patient did not show.

Secondary outcomes

  1. Appointment Completion Rate

    Time frame: Through study completion, on average of 3 weeks

    Proportion of initial scheduled appointments completed.

  2. Appointment Cancelation Rate

    Time frame: Through study completion, on average of 3 weeks

    Proportion of initially scheduled appointments cancelled.

  3. Appointment Refill Rate

    Time frame: Through study completion, on average of 3 weeks

    Proportion of cancelled appointments that were refilled.

  4. Refilled Appointment Completion Ration

    Time frame: Through study completion, on average of 3 weeks

    Proportion of refilled appointments that were completed.

  5. Net Appointment Completion Rate

    Time frame: Through study completion, on average of 3 weeks

    Proportion of appointment slots resulting in a completed appointment. Includes completed refilled appointments.

Sponsors and collaborators

Lead sponsor

M. Kit Delgado, MD

Other

Registry information

Official study title

Comparative Effectiveness of Targeted Outreach With an Automated Caller for Increasing Appointment Completion: A Randomized Quality Improvement Initiative

Important dates

Study start
2024
Primary completion
2024
Study completion
2025
First posted
Jan 9, 2025
Registry last updated
Apr 4, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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