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OpenTrials
Completed

NCT Number: NCT02903849

Using Self-Motivating Messages to Encourage People to Exercise More

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

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Hengchen Dai

St Louis, Missouri, 63108, United States

About this study

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).

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Drafting Motivational Messages

Behavioral

Write down three motivating messages

Control Reminders

Behavioral

Receive standard reminders at three points during the challenge

Treatment Reminders

Behavioral

Receive reminders containing the messages they leave themselves at three points during the challenge

Primary outcomes

  1. Activity Level

    Time frame: Through study completion, 100 days

    Number of steps taken each day, as recorded in participants' online portal.

Secondary outcomes

  1. Body Mass Index (BMI)

    Time frame: After the 100-day challenge ends

    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.

  2. Cholesterol

    Time frame: After the 100-day challenge ends

    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.

  3. Blood Pressure

    Time frame: After the 100-day challenge ends

    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.

  4. Stress

    Time frame: After the 100-day challenge ends

    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.

Sponsors and collaborators

Lead sponsor

Washington University School of Medicine

Other

Collaborators

  • University of California, Los Angeles

Registry information

Important dates

Study start
2016
Primary completion
2016
Study completion
2017
First posted
Sep 16, 2016
Registry last updated
May 9, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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