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Physical ActivityNCT05110508

Active KC: a Text Message Based Intervention for Physical Activity

A study testing Text Based Behavioral Intervention for Physical Activity in people with Physical Activity and Patient Engagement, 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

Active KC will involve delivering PA support tools to individuals interested in increasing their physical activity. The tools involve provision of a Garmin wearable activity monitor and participant-tailored behavior change supports (e.g., goal setting and monitoring) delivered through text messaging and a… Read more about this study

Who is it for?
Ages 8 years and olderHealthy volunteers can take part
Conditions the study is for
Physical Activity, Patient Engagement
What is being tested?
Text Based Behavioral Intervention for Physical Activity
Could I receive a placebo?
No, everyone receives an active treatment
How many people
210 participants
Where
1 siteUnited States
Study dates
25 Sep 2021to 30 Apr 2022
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 8 years and older
  • All sexes
  • Healthy volunteers accepted
  • Child, Adult, Older adult

Who may be able to join

  • Individual has a smart device with internet or data and app downloading and texting capability
  • Can read or write in English
  • At least 8 years old (there is no upper age limit)
  • Willing to complete study measures, participate in intervention, and share data collected in Active KC with the main study

Who cannot join

  • Does not meet the above inclusion criteria
  • Non-adherent to study measurement (wearing the Garmin less than 4 days) during baseline period
  • Averaging over 60 minutes per day of physical activity (children) or 30 minutes of physical activity per day (adults) during the baseline period as measured by the Garmin
  • Participant has a disability that interferes with their ability to carry out daily activities

Trial locations and contacts

1 site in 1 country.

United States1 site
  • Children's Mercy

    Kansas City, Missouri, 64108

Other trials in United States

About this study

Active KC will involve delivering PA support tools to individuals interested in increasing their physical activity. The tools involve provision of a Garmin wearable activity monitor and participant-tailored behavior change supports (e.g., goal setting and monitoring) delivered through text messaging and a corresponding study website.

Being tested
Text Based Behavioral Intervention for Physical Activity
Keywords
text message, technology, Garmin, physical activity
Medical subject headings
Motor Activity, Patient Participation

What participants receive

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

  • Text Based Behavioral Intervention for Physical ActivityBehavioural

    Text intervention messaging will be sent through an automated text messaging service programmed by the CM Informatics team, which has been approved by the institution. Participants will be asked to wear Garmin physical activity monitor to provide physical activity information throughout the intervention. The Garmin is worn like a wristwatch. The device is small and non-intrusive. The Garmin device is a consumer wearable that will automatically detect and track activity such as walking, running, and cycling. The text messages incorporate information from the Garmin monitor to support physical activity.

Study groups in NCT05110508
Study groupRoleWhat they receive
Physical Activity Self-RegulationExperimentalParticipants will receive multiple weekly text messages. Texts will contain wear reminders, encouragements, congratulatory content, and behavior change messages based on the Garmin data. Some text message content asks for a response from the participant to help tailor later messages for behavior change support.
Receives: Behavioral: Text Based Behavioral Intervention for Physical Activity

What is being measured

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

  1. Changes in Physical Activity Minutes Over Time

    Participant physical activity will be measured by daily minutes of physical activity as collected by the Garmin monitor.

    Measured: 8 weeks

  2. Changes in Physical Activity Steps Over Time

    Participant physical activity will be measured by a daily step count as collected by the Garmin monitor.

    Measured: 8 weeks

Secondary outcomes (4)
  1. Participant Engagement of Text Messages

    Text message engagement as measured by number of texts responded to.

    Measured: 8 weeks

  2. Views of Participants on Intervention Preferences via Participant Survey

    Adults will complete a baseline and follow up adult survey and children will complete a baseline and follow up child survey with help from their caregiver when appropriate. Participant surveys may be distributed via hardcopy, email, or text message.

    Measured: Baseline, End of Study (8 weeks)

  3. Participant Engagement of the Garmin Monitor

    Garmin activity monitor engagement as measured by number of wear days.

    Measured: 8 weeks

  4. Views of Participants on intervention via Focus Groups

    Up to 15 focus groups will be hosted throughout and after the intervention period. A subsample of participants will be selected to take part in focus groups conducted after week 4 and week 8. These focus groups will ask about participant experiences with the Garmin monitors and text messaging along with general perceptions of the intervention. Focus groups will be hosted virtually using Teams or in person and will be recorded. All participants will have the option to keep their cameras off during virtual focus groups.

    Measured: Week 4, Week 8

Timeline

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

  1. First posted8 Nov 2021
  2. Study start25 Sep 2021
  3. Primary completion30 Apr 2022
  4. Study completion30 Apr 2022

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
Prevention
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
210 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05110508
Sponsor's protocol ID
STUDY00001939
Status last verified
Feb 2025
First submitted
9 Sep 2021
Last updated
12 Feb 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Publications

  • Carlson JA, Materia F, Moon M, Ryu S, Yeager C, Steel C, Shields K, Gill HS, Berkley-Patton J, Catley D. Automated Physical Activity Support for Adults and Youth From Low-Income Communities: Single-Arm Pilot Study. JMIR Mhealth Uhealth. 2026 Jun 5;14:e76991. doi: 10.2196/76991.

    PubMed 42247677

Questions about this trial

What is this clinical trial studying?

A study testing Text Based Behavioral Intervention for Physical Activity in people with Physical Activity and Patient Engagement, 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 4 inclusion and 4 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 12 Feb 2025. 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?

Changes in Physical Activity Minutes Over Time (time frame: 8 weeks). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT05110508, which also lists 1 linked publication.

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 12 Feb 2025.

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