Evive Health Randomized Controlled Trials

September 27, 2017 updated by: University of Pennsylvania
The mailer will encourage those who are due for mammograms, colonoscopies, blood pressure or cholesterol tests to receive the appropriate test. This particular mailer will only be sent to Evive clients in need to the test in question. The research will examine differences in follow-through on this recommendation among the targeted population over the 3-12 month period following the mailing as a function of experimental condition.

Study Overview

Study Type

Interventional

Enrollment (Actual)

29

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

    • Pennsylvania
      • Philadelphia, Pennsylvania, United States, 19104
        • University of Pennsylvania

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:

  • Employee at partner corporation
  • Due for mammogram, colonoscopy, blood pressure or cholesterol test

Exclusion Criteria:

  • Already received mammogram, colonoscopy, blood pressure or cholesterol test

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: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Control
On top of reminder, state: "Here's a fun fact to cheer you on your way:" and include a curiosity-inducing question and answer (e.g., "Q: Which is the only state that allows you to cast absentee ballots from outer space? // A: Texas")
No scratch off element
Experimental: Curiosity
On top of reminder, state: "Here's a fun fact to cheer you on your way." and include a curiosity-inducing question (e.g., "Q: Which is the only state that allows you to cast absentee ballots from outer space?") Place the answer under a scratch-off patch ("A: Texas").
The recipient will be prompted to scratch off for answer to question.
Experimental: Curiosity linked to Action
On top of reminder, state: "Here's a fun fact to cheer you on your way. Reward yourself by scratching off the answer only after you've made your [colonoscopy/mammogram/etc.] appointment!" and include a curiosity-inducing question (e.g., "Q: Which is the only state that allows you to cast absentee ballots from outer space?") Place the answer under a scratch-off patch ("A: Texas")
The recipient will be prompted to scratch off for answer only after he/she makes an appointment.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Number of Participants who follow-through from the mailing
Time Frame: three to twelve months
three to twelve months

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

August 1, 2014

Primary Completion (Actual)

October 1, 2014

Study Completion (Actual)

October 1, 2014

Study Registration Dates

First Submitted

July 26, 2012

First Submitted That Met QC Criteria

July 26, 2012

First Posted (Estimate)

July 30, 2012

Study Record Updates

Last Update Posted (Actual)

September 28, 2017

Last Update Submitted That Met QC Criteria

September 27, 2017

Last Verified

September 1, 2017

More Information

Terms related to this study

Other Study ID Numbers

  • 813606-3

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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