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A Mobile Phone Text-based Intervention to Reduce Sedentary Behavior and Engage Communities on the Importance of Healthy Lifestyles: the TEXT2MOVE Study

A Mobile Phone Text-based Intervention to Reduce Sedentary Behavior and Engage Communities on the Importance of Healthy Lifestyles: the TEXT2MOVE Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05217108
Enrollment
228
Registered
2022-02-01
Start date
2022-01-05
Completion date
2026-10-31
Last updated
2026-05-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy Lifestyle, Life Style

Brief summary

To learn if an 8-week, phone-based texting intervention program will reduce sedentary (non-mobile) behavior.

Detailed description

Primary Objective: To test the effect of two text messaging strategies, responsive texts and standard scheduled texts, on sedentary behavior in a racially and geographically diverse sample of adults. Secondary Objective: To assess participant engagement with the program and with the educational content delivered via text messaging. Exploratory Objective: To determine whether two text messaging strategies, responsive texts and standard scheduled texts, increases physical activity in a racially and geographically diverse sample of adults. Exploratory Objective: To determine whether two text messaging strategies, responsive texts and standard scheduled texts are associated with changes in corresponding patient attitudes as assessed by surveys of exploring sedentary behavior, readiness for exercise change, and physical functioning.

Interventions

DEVICEFitBit

All participants in each study group will receive a Fitbit. Participants will be asked to wear a Fitbit every day for 8 weeks to record the number of steps you take

Sponsors

M.D. Anderson Cancer Center
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

1. \>18 years old 2. owns a smart phone 3. has access to WiFi or willing to use mobile data 4. has an email address or willing to create an email address 5. able to read and understand English; 6. able to give informed consent; 7. willing to receive text messages and complete brief questionnaires on their smart phone 8. self-reports sedentary behavior (\> 6 hours/day of sitting time).

Exclusion criteria

1. unwilling to have sedentary behavior and activity tracked 2. unable to walk without ambulatory assistance device (i.e. cane or walker) or due to underlying medical condition 3. MD Anderson employees that report to the Principal Investigators of this study 4. family or household member already enrolled into study 5. not sedentary based on \< 6 hours/day of sitting time, and (6) currently participating in a weight management or exercise study or program

Design outcomes

Primary

MeasureTime frame
Daily minutes in sedentary behavior based on Fitbit data.through study completion, an average of 1 year

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORKaren Basen-Engquist, MD

M.D. Anderson Cancer Center

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 23, 2026