Mechanisms Behind Benefits Framing

May 6, 2026 updated by: University of Chile
This study evaluates the effectiveness of different message framings used to encourage uptake of preventive dental check-ups. Patients will be randomized to receive one of several WhatsApp messages offering a full preventive dental check-up, which vary in message length and in how the benefits of the check-up are described.

Study Overview

Detailed Description

Patients in this trial will be randomized to one of four conditions. In all conditions, patients will receive a WhatsApp message from a clinic network, encouraging them to schedule a preventive dental check-up. The conditions vary in message length and the specificity of the benefits emphasized. Previous pilot studies run by the investigators suggest that adding health- or appearance-related meaning to preventive dental checkup invitation messages may reduce uptake relative to a basic WhatsApp invitation. The present study is designed to replicate this pattern and explore the mechanism(s) underlying this pattern by isolating the role of message length and the references to benefits. Specifically:

  1. Basic Outreach Message: Patients receive a brief outreach message inviting them to schedule a preventive dental check-up and providing basic information about price and availability.
  2. Expanded Neutral Outreach Message: Patients receive a longer outreach message matched in length to the benefit-focused messages (see below), which adds only neutral wording to the Basic Outreach Message without introducing any additional information.
  3. Expanded Generic Benefit Outreach Message: Patients receive a longer outreach message that emphasizes general benefits from a preventive dental check-up, without referencing specific outcomes related to dental health or appearance.
  4. Expanded Specific Benefit Outreach Message: Patients receive a longer outreach message that highlights specific benefits of a preventive dental check-up. Within this condition, patients are further randomly assigned to receive one of four message variants that independently vary (1) whether the benefit emphasized relates to dental health or appearance and (2) whether the benefit is framed as occurring immediately or in the long term.

The researchers primarily ask the following research question: Does emphasizing specific benefits in an expanded outreach message affect dental check-up uptake relative to a basic outreach message? The researchers hypothesize that patients receiving the Expanded Specific Benefit Outreach Message will have lower uptake of dental checkups than patients receiving the Basic Outreach Message. The investigators will also assess the roles of message length and language referencing benefits.

Analysis:

The investigators will run ordinary least squares regressions (OLS) with robust standard errors to predict outcome variables.

  1. To test whether emphasizing specific benefits in an expanded outreach message affect uptake relative to a basic outreach message, the investigators will pool (collapse) the four variants of the Expanded Specific Benefit Outreach Message condition into a single treatment indicator and compare outcomes for patients assigned to this pooled condition versus patients assigned to the Basic Outreach Message condition.

    In addition, the investigators will estimate a model that includes indicators for each of the four specific-benefit variants and conduct a joint F-test of whether the four variant indicators are jointly equal (i.e., whether outcomes differ across the variants).

  2. The investigators will conduct additional comparisons to understand why the Expanded Specific Benefit Outreach message may reduce uptake relative to the Basic Outreach message. Specifically, the investigators will compare outcomes between the Basic Outreach Message condition versus the Expanded Neutral Outreach Message condition to assess the role of message length. If there is no significant difference between the two treatments, they will be pooled and compared to the Specific Benefit (pooled) treatments. Then the investigators will compare outcomes between the Basic Outreach Message condition versus the Expanded Generic Benefit Outreach Message condition to assess the role of message length and language referencing benefits.

These regressions will be run with and without control variables. Control variables include:

  • Time fixed effects (since patients will be enrolled into the trial over time)
  • Participant age
  • Participant gender (male, female, other/unknown)
  • Whether patients had had at least one dental visit at this hospital in the past
  • Region or clinic indicators, if available

For robustness, the investigators will conduct logit models as well.

The investigators will examine whether the following factors moderate the differences in uptake between the Expanded Specific Benefit Outreach Message condition and Basic Outreach Message condition:

  • Whether the patient had completed any dental visit prior to the experiment (based on the data the hospital can provide)
  • Whether the patient had completed any preventive medical exam (e.g., mammogram) prior to the experiment (based on the data the hospital can provide)
  • Whether participants attended a non-dental medical appointment the day before contact (vs. have a non-dental medical appointment scheduled after the contact day)
  • Number of prior visits to the clinic network that were not for dental purposes (based on the data the hospital can provide) prior to the contact (excluding the visit that some of the participants had the day before the contact)
  • Insurance type (public vs. private)
  • Patient age
  • Patient gender (male vs. female)

For exploratory purposes, the investigators will look at longer time windows (e.g., 90 days) for dental appointment attendance and will also examine behaviors related to the dental appointments (e.g., cancellation, rescheduling, no-show).

Study Type

Interventional

Enrollment (Estimated)

100000

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Santiago, Chile
        • Partnering clinic network

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • Patients aged 18 and above
  • Have a valid mobile phone number that can receive WhatsApp messages, recorded in the hospital network's patient database
  • Attended a non-dental medical appointment the day before the intended contact day OR have a non-dental medical appointment within the week after the intended contact day
  • Have not been contacted in the past two months about preventive dental checkups
  • Have not attended a dental appointment at the hospital network in the past 6 months

Note: The partnering clinic agreed to run the study until a concurrent experiment registered at NCT07121673 is finished. The investigators aim to reach 100,000 patients by then, but the final sample size will vary depending on the actual outreach efforts by the end of the study period.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Health Services Research
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: Basic Outreach Message
Basic dental appointment message
Patients receive a short WhatsApp message encouraging them to schedule a preventive dental check-up
Experimental: Expanded Neutral Outreach Message
Expanded neutral dental appointment message
Patients receive an expanded WhatsApp message encouraging them to schedule a preventive dental check-up, which adds neutral words to the Basic Outreach Message without introducing new information.
Experimental: Expanded Generic Benefit Outreach Message
Expanded generic benefit dental appointment message
Patients receive an expanded WhatsApp message encouraging them to schedule a preventive dental check-up, emphasizing general benefits of doing so.
Experimental: Expanded Specific Benefit Outreach Message
Expanded specific benefit dental appointment message
Patients receive one of four expanded WhatsApp messages encouraging them to schedule a preventive dental check-up that highlights specific benefits related to dental health or appearance, with patients randomly assigned to one of the four variants.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Preventive Dental appointment scheduling
Time Frame: Within 7 days of receiving the WhatsApp message
Whether the patient schedules a preventive dental check-up
Within 7 days of receiving the WhatsApp message

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Preventive Dental appointment attendance
Time Frame: Within 30 days of receiving the WhatsApp message
Whether the patient attends a preventive dental check-up
Within 30 days of receiving the WhatsApp message
Interest in scheduling
Time Frame: Within 7 days of receiving the WhatsApp message
Whether the patient clicks YES in response to the WhatsApp message
Within 7 days of receiving the WhatsApp message
Any dental appointment scheduling
Time Frame: Within 7 days of receiving the WhatsApp message
Whether the patient schedules any dental appointment (regardless of whether it is preventive or not)
Within 7 days of receiving the WhatsApp message

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

January 26, 2026

Primary Completion (Actual)

February 28, 2026

Study Completion (Estimated)

May 1, 2026

Study Registration Dates

First Submitted

January 22, 2026

First Submitted That Met QC Criteria

May 6, 2026

First Posted (Actual)

May 14, 2026

Study Record Updates

Last Update Posted (Actual)

May 14, 2026

Last Update Submitted That Met QC Criteria

May 6, 2026

Last Verified

January 1, 2026

More Information

Terms related to this study

Other Study ID Numbers

  • Dentistry_Benefits_Mechanisms

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

IPD will not be shared due to restrictions in the data use agreement with the partnering clinic network, which prohibits public dissemination of patient-level data.

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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