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Bemobile Intervention to Support Physical Activity in Cancer Survivors

Bemobile: A Text Intervention to Support Physical Activity in Cancer Survivors

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02824861
Enrollment
70
Registered
2016-07-07
Start date
2015-07-31
Completion date
2018-11-01
Last updated
2019-04-17

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

Conditions

Cancer

Brief summary

This study evaluates a technology based intervention (physical activity tracker, text messages, health coach, global positioning system enabled location based feedback on physical activity) to support physical activity in cancer survivors after completing oncology rehabilitation. In Phase 1 all participants received the full intervention. In phase II participants are randomly assigned to receive the full intervention or a fitbit only.

Detailed description

This intervention, offered to participants after completing oncology rehabilitation, integrates known preferences and determinants of physical activity participation in women and breast cancers survivors including social support, professional guidance, self-efficacy, goal setting, self-regulation, and environmental awareness delivered through accessible technology. For the iteration phase, the investigators will conduct an initial, abbreviated intervention wave lasting 4 weeks; the investigators will then incorporate participant input and feedback on the specific components to refine the intervention prior to a pilot trial. Means of delivering the components include communication and support through tailored text messaging, health coaching phone calls, self-monitoring of physical activity through a wearable sensor, and environmental assessment of community physical activity options (e.g., parks, fitness centers, trails) based on global positioning system information.

Interventions

BEHAVIORALBemobile

Sponsors

University of Vermont
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
22 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Cancer diagnosis * Impending graduation from oncology rehabilitation

Exclusion criteria

* Metastatic cancer * Concurrent radiation or chemotherapy * No cell phone * Inability to read or speak English.

Design outcomes

Primary

MeasureTime frameDescription
Change from Baseline in Step counts8 weeksMean daily step counts as assessed by Actigraph Accelerometer
Change from Baseline in Moderate to Vigorous Physical Activity (MVPA)8 weeksWeekly accumulated minutes spent in MVPA as assessed by Actigraph Accelerometer

Secondary

MeasureTime frameDescription
Change in Weekly average of mean daily step counts8 weeksStep counts assessed during the intervention with the Fitbit One
Change from Baseline in Self-efficacy to perform exercise8 weeksScale developed by Garcia and King
Change from Baseline in Self-regulation8 weeksScale Developed R. Umstattd
Change from Baseline in Fatigue8 weeksFatigue Symptom Inventory (FSI)

Countries

United States

Outcome results

None listed

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