The Effect of Active Choice on Nurse Visit Participation

The Effect of Time-Slot Scheduling and Active Choice on Biometric Screening and Nurse Visit Participation

The goal of this project is to see if behavioral nudges will increase an individual's likelihood of participating in a nurse visit. The behavioral nudges under consideration are encouraging subjects to make an active choice and sending reminders.

Study Overview

Detailed Description

The employees in our sample will schedule their nurse visit time slot via e-mail and a health service provider website. Much as is the case in the current system, the control group will be informed via e-mail of the window of dates during which they can take part in the on-site screening and given instructions for scheduling an appointment. The treatment group, the active choice only arm, will be given the same information as the control group, but they will also be asked to make an appointment immediately, defer the scheduling decision, or decline to receive a screening. The treatment group will also receive email reminders one week before their appointment.

Study Type

Interventional

Enrollment (Actual)

3500

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

    • Nevada
      • Las Vegas, Nevada, United States, 89119
        • Caesars Corporate Office

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

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Harrah's employee
  • Registered e-mail address with Harrah's
  • Part of Harrah's Choosing Wellness Program

Exclusion Criteria:

  • Under 18
  • Already participated in a nurse visit

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: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Other: Control Arm
The control group will be informed via e-mail of the window of dates during which they can take part in the on-site screening and given instructions for scheduling an appointment.

The goal of this project is to see if active choice will increase an individual's likelihood of participating in a nurse visit.

The employees in our sample will schedule their nurse visit time slot via e-mail and a health service provider website. The control group will be informed via e-mail of the window of dates during which they can take part in the on-site screening and given instructions for scheduling an appointment. The treatment group, the active choice only arm, will be given the same information as the control group, but they will also be asked to make an appointment immediately, defer the scheduling decision, or decline to receive a screening. The treatment group will also receive email reminders one week before their appointment.

Other Names:
  • Active Choice and Participation
Experimental: Active Choice Only Arm
The active choice only arm, will be given the same information as the control group, but they will also be asked to make an appointment immediately, defer the scheduling decision, or decline to receive a screening.

The goal of this project is to see if active choice will increase an individual's likelihood of participating in a nurse visit.

The employees in our sample will schedule their nurse visit time slot via e-mail and a health service provider website. The control group will be informed via e-mail of the window of dates during which they can take part in the on-site screening and given instructions for scheduling an appointment. The treatment group, the active choice only arm, will be given the same information as the control group, but they will also be asked to make an appointment immediately, defer the scheduling decision, or decline to receive a screening. The treatment group will also receive email reminders one week before their appointment.

Other Names:
  • Active Choice and Participation

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Nurse Visit Participation
Time Frame: This will be measured after all of the nurse visit windows have been closed, by 4/30/11
We will measure whether or not subjects scheduled and participated in a nurse visit. We will compare the number of subjects who participated in the nurse visits by treatment arms.
This will be measured after all of the nurse visit windows have been closed, by 4/30/11

Collaborators and Investigators

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

Investigators

  • Principal Investigator: David I Laibson, Ph.D, National Bureau of Economic Research

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

December 1, 2010

Primary Completion (Actual)

January 1, 2012

Study Completion (Actual)

January 1, 2012

Study Registration Dates

First Submitted

November 29, 2010

First Submitted That Met QC Criteria

November 29, 2010

First Posted (Estimate)

November 30, 2010

Study Record Updates

Last Update Posted (Estimate)

May 18, 2012

Last Update Submitted That Met QC Criteria

May 16, 2012

Last Verified

May 1, 2012

More Information

Terms related to this study

Other Study ID Numbers

  • 0001 (Researcher)
  • P30AG034532 (U.S. NIH Grant/Contract)

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 Participation in Nurse Visits

Clinical Trials on The Effect of Active Choice on Nurse Visit Participation

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