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Evaluation of a Smartphone Intervention to Reduce Sedentary Behavior

Evaluation of a Smartphone Intervention to Reduce Sedentary Behavior

Status
Withdrawn
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03094858
Acronym
SMARTpath
Enrollment
0
Registered
2017-03-29
Start date
2019-03-01
Completion date
2020-04-30
Last updated
2021-06-11

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

Conditions

Risk Reduction Behavior

Keywords

Smartphone, sedentary behavior, smartphone intervention

Brief summary

Participants (N = 300) will be randomly assigned to: 1) an equipment-only comparison group that receives a smartphone and an activity monitor wristband but does not receive smartphone intervention prompts, or 2) the intervention group who will receive an activity monitor wristband that works in conjunction with a smartphone to reduce sedentary time via smartphone prompts during prolonged sedentary bouts. All participants will be provided with a Fitbit® wristband activity monitor and an Android smartphone on the same day of the week (i.e., Mondays). Participants will complete a 1-week baseline accelerometer and EMA period prior to the start of the intervention. Participants will be followed for 26 weeks after the intervention begins with follow-up visits at 6, 13, and 26 weeks. The primary outcome will be accelerometer-measured time spent in sedentary activity. Sedentary breaks, total active time, and time spent in light, moderate, and vigorous activity will be additionally evaluated as outcomes. Contextual variables and potential treatment mechanisms will be assessed via traditional questionnaire measurement and daily random EMAs at baseline and all follow-up visits. Brief smartphone-based daily diary assessments will be completed daily for the duration of the study.

Interventions

DEVICESmartphone with prompts

Smartphone will be used to prompt randomly selected participants in intervention group to be active

DEVICEWristband

Wristband will monitor activity of all participants

DEVICESmartphone

Smartphone will be used to monitor activity but prompts will not be given to randomly selected participants

Sponsors

University of Oklahoma
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 99 Years
Healthy volunteers
Yes

Inclusion criteria

* A score of ≥ 4 on the REALM-SF85 indicating \> 6th grade English literacy level, must be at least 18 years of age * A BMI ≥ 25 (overweight/obese), not meeting current physical activity guidelines as measured by the 7-Day Physical Activity Recall * Do not have a contraindication for physical activity based on the Physical Activity Readiness Questionnaire (PAR-Q) * Able to attend all study visits, and possess a valid home address and a functioning telephone number.

Exclusion criteria

* Participants who have physical disabilities that restrict lower limb function and/or reading skills below a 7th grade reading level.

Design outcomes

Primary

MeasureTime frameDescription
Accelerometer-measured sedentary timeOne weekTotal accelerometer-measured time spent in sedentary activity

Secondary

MeasureTime frameDescription
Accelerometer-measured sedentary breaks26 weeksAccelerometer-measured time spent in sedentary activity
Accelerometer-measured total active time26 weeksTotal active time
Accelerometer-measured time spent in light, moderate, and vigorous activity26 weeksTotal time spent in light, moderate, and vigorous activity

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026