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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02903849
Other study ID # 2016080382
Secondary ID
Status Completed
Phase N/A
First received September 13, 2016
Last updated May 8, 2017
Start date September 2016
Est. completion date January 2017

Study information

Verified date May 2017
Source Washington University School of Medicine
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The investigators are interested in using personalized, self-motivating messages to motivate people to exercise more.


Description:

The investigators are interested in using personalized, self-motivating messages to motivate people to exercise more. Through a partnership with a university, the investigators are running a large-scale, randomized field controlled trial aimed at increasing exercise frequencies during a 100-day challenge. The primary purpose of this study is to test whether sending people motivating messages they wrote to themselves in the past can keep them engaged in the challenge and motivate them to exercise more frequently. One week into the challenge, employees who have signed up for the challenge will receive an email inviting them to participate in a short activity. Employees who click on the link will be directed to a survey. Once they finish reading the first introductory page and click "next", they will be randomly assigned to one of two groups. In the control group, employees will be encouraged to write down what they think will motivate them to walk more after 20, 50, and 90 days into the Challenge. These employees will receive standard reminders on the 20th, 50th, and 90th day of the challenge. In the treatment group, employees will be encouraged to write down motivating messages that they will receive on the 20th, 50th, and 90th day of the Challenge.

All employees who are exposed to either the control or the treatment condition will be included in the analysis.

The investigators plan to explore moderators based on (a) employees' demographics (age, gender, ethnicity, position), (b) employees' participation in previous challenges, and (c) employees' health condition and fitness level prior to the challenge (such as how actively they have been participating in other wellness activities, their health statistics).


Recruitment information / eligibility

Status Completed
Enrollment 324
Est. completion date January 2017
Est. primary completion date December 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Employees who click on the link inviting them to participate in an activity and are assigned to either the treatment or control condition

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Drafting Motivational Messages
Write down three motivating messages
Control Reminders
Receive standard reminders at three points during the challenge
Treatment Reminders
Receive reminders containing the messages they leave themselves at three points during the challenge

Locations

Country Name City State
United States Hengchen Dai Saint Louis Missouri

Sponsors (2)

Lead Sponsor Collaborator
Washington University School of Medicine University of California, Los Angeles

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Activity Level Number of steps taken each day, as recorded in participants' online portal. Through study completion, 100 days
Secondary Body Mass Index (BMI) Most recent BMI in pounds (weight) and inches (height) as entered by participant, an expected average of 2 months after study start. Obtaining the data is dependent on the ability to obtain the data from the online portal. After the 100-day challenge ends
Secondary Cholesterol Most recent total, low, and high cholesterol levels in mg/dl as entered by participant, an expected average of 2 months after study start. Obtaining the data is dependent on the ability to obtain the data from the online portal. After the 100-day challenge ends
Secondary Blood Pressure Most recent systolic and diastolic levels in mmHg as entered by participant, an expected average of 2 months after study start. Obtaining the data is dependent on the ability to obtain the data from the online portal. After the 100-day challenge ends
Secondary Stress Most recent self-reported stress level on a 1-5 scale (with 1 indicating "Relaxed" and 5 indicating "Highly Stressed") as entered by participant, an expected average of 2 months after study start. Obtaining the data is dependent on the ability to obtain the data from the online portal. After the 100-day challenge ends
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