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Physical ActivityNCT06873139

FIT4Life Text Message Program

A study testing text messages in people with Physical Activity and Behavior Change, run by Children's Mercy Hospital Kansas City at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

FIT4Life is a text message based physical activity project that includes one baseline week and 26 weeks of intervention delivery. Study participants will be provided with fitness trackers to support their physical activity goals. Read more about this study

Who is it for?
Ages 18 years and olderHealthy volunteers can take part
Conditions the study is for
Physical Activity, Behavior Change
What is being tested?
text messages
Could I receive a placebo?
No, everyone receives an active treatment
How many people
98 participants
Where
1 siteUnited States
Study dates
25 Mar 2025to 27 Jan 2026
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • 18 years or older
  • Able to read, write, and speak English
  • Currently a Diabetes Prevention Program group or in a similar group that is recruited by the external community partner (Our Healthy Jackson County)

Who cannot join

  • Does not meet the inclusion criteria listed above

Trial locations and contacts

1 site in 1 country.

United States1 site
  • Kansas City Community

    Kansas City, Missouri, 64108

Other trials in United States

About this study

FIT4Life is a text message based physical activity project that includes one baseline week and 26 weeks of intervention delivery. Study participants will be provided with fitness trackers to support their physical activity goals. The text messages are intended to motivate participants to engage in physical activity throughout the week, but do not prescribe specific exercises/workout regimens for participants to follow.

Being tested
text messages
Medical subject headings
Motor Activity

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • text messagesBehavioural

    There will be two arms for the texting intervention: high and low. Both arms will receive text messages, but the frequency of the messages will vary by arm. Text intervention messaging will be sent through an automated text messaging service programmed by the CM Research Informatics team, which has been approved by the institution.

Study groups in NCT06873139
Study groupRoleWhat they receive
High ArmExperimentalHigh-arm participants will receive daily messages related to wear reminders, encouragements, congratulatory content, and behavior change based on the activity tracker data. Step counts from the activity tracker are included in some messages to track and facilitate step goals. Some text message content asks for a response from the participant to help tailor later messages for behavior change support.
Receives: Behavioral: text messages
Low ArmExperimentalLow arm participants will receive weekly messages related to reminders to wear their activity tracker and tips on how to use the tracker.
Receives: Behavioral: text messages

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Acceptability and preferences

    Descriptive analyses will be used to analyze the survey data and qualitative thematic analyses will be used to analyze interview data to determine participant preferences and program acceptability.

    Measured: From enrollment to the end of program at 27 weeks

Secondary outcomes (2)
  1. Change in Physical Activity Minutes

    Longitudinal models will be used to investigate changes in physical activity minutes over time, from before (baseline) to after the intervention.

    Measured: From enrollment to the end of program at 27 weeks

  2. Change in Physical Steps

    Longitudinal models will be used to investigate changes in steps over time, from before (baseline) to after the intervention.

    Measured: From enrollment to the end of program at 27 weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted12 Mar 2025
  2. Study start25 Mar 2025
  3. Primary completion27 Jan 2026
  4. Study completion27 Jan 2026

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Other
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Participant
Enrolment
98 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06873139
Sponsor's protocol ID
STUDY00003517
Status last verified
Apr 2026
First submitted
20 Feb 2025
Last updated
27 Apr 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: Participant data will be aggregated and shared to protect privacy.

Questions about this trial

What is this clinical trial studying?

A study testing text messages in people with Physical Activity and Behavior Change, run by Children's Mercy Hospital Kansas City at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 27 Apr 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Acceptability and preferences (time frame: From enrollment to the end of program at 27 weeks). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 27 Apr 2026; AzTrials last refreshed its copy on 27 Oct 2026.

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