The Power of Curiosity: Leveraging Curiosity to Motivate People to Complete Health Risk Assessments

August 29, 2016 updated by: Todd Rogers, Harvard University

The Power of Curiosity

The investigators will work with one of Vitality's partner corporations to test whether curiosity can motivate employees to follow through on their virtuous intentions and complete their annual health risk assessment (VHR). Employees will receive email messages that contain either a curiosity-inducing question or a standard encouragement message. The investigators predict that presenting people with curiosity-arousing questions will make them more likely to complete a health risk assessment, as compared to standard messages.

Study Overview

Detailed Description

The vast majority of adults express the desire and intention of engaging in healthy behaviors-exercising, losing weight, getting a colonoscopy-but then fail to do so. This has massive individual and societal costs. This research tests a promising intervention to increase the likelihood that an adult will follow through on their health-related intentions. Curiosity can be a powerful motivator and can cause people to engage in new behaviors (Tomkins 1962; Silvia 2006); however, curiosity has not yet been used as an intervention to help people follow-through on their intentions. In this project, the investigators target employees who have failed to complete their annual Vitality Health Review (VHR) and test whether curiosity can be used to induce the employees to complete their VHR. The VHR is a medical questionnaire that can help individuals understand medical risk factors they may be prone to. The investigators provide employees with a question and inform them that they will see the answer upon completion of their VHR. The investigators hypothesize that the curiosity-inducing messages will cause employees to follow through on their intention to complete their VHR.

Study Type

Interventional

Enrollment (Actual)

10095

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

    • Massachusetts
      • Cambridge, Massachusetts, United States, 02138
        • Harvard Kennedy School

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

18 years and older (ADULT, OLDER_ADULT)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Employees at Vitality's partner's worksites that are in Vitality database
  • Must have email address on file

Exclusion Criteria:

  • Employees that have already completed their VHR by June 11, 2013

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
  • Masking: SINGLE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
EXPERIMENTAL: Standard Message
Participants will receive email messages that encourage them to complete their VHR.
Participants will receive email messages that contain "standard" language encouraging them to complete their VHRs (health review that can be completed online).
EXPERIMENTAL: Curiosity Message
Participants receive email messages containing "curiosity-inducing" questions. The messages tell the participants that they will receive the answer to the question after they complete their VHR.
Participants will receive email messages that contain one of 8 curiosity-inducing questions. The message will tell participants that they will receive a message with the answer after they complete their VHR (health review that can be completed online).

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Completion of VHR
Time Frame: Measured one month after first message (July 12, 2013)
Whether the participant completes his/her VHR or not
Measured one month after first message (July 12, 2013)

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Previous VHR Completion during 2012-2013
Time Frame: On or before July 12, 2013
Whether employee completed their VHR the previous year
On or before July 12, 2013
Social Atmosphere at Worksite
Time Frame: On or before August 12, 2013
Measured by post-intervention survey with questions about how frequently employees at worksite interact and discuss non-work and Vitality-related matters
On or before August 12, 2013
Curiosity Type
Time Frame: On or before July 12, 2013
For participants who receive "curiosity" messages, indicates which curiosity message they received.
On or before July 12, 2013

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Todd Rogers, PhD, Harvard University
  • Principal Investigator: Erin Frey, Harvard University

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

June 1, 2013

Primary Completion (ACTUAL)

November 1, 2013

Study Completion (ACTUAL)

November 1, 2013

Study Registration Dates

First Submitted

June 7, 2013

First Submitted That Met QC Criteria

June 10, 2013

First Posted (ESTIMATE)

June 12, 2013

Study Record Updates

Last Update Posted (ESTIMATE)

August 31, 2016

Last Update Submitted That Met QC Criteria

August 29, 2016

Last Verified

August 1, 2016

More Information

Terms related to this study

Other Study ID Numbers

  • F24176-101

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.

Clinical Trials on Intention

Clinical Trials on Standard Message

Subscribe