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Clinical Trials/NCT02824861
NCT02824861
Completed
Not Applicable

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

University of Vermont1 site in 1 country70 target enrollmentJuly 2015
ConditionsCancer

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Cancer
Sponsor
University of Vermont
Enrollment
70
Locations
1
Primary Endpoint
Change from Baseline in Step counts
Status
Completed
Last Updated
7 years ago

Overview

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.

Registry
clinicaltrials.gov
Start Date
July 2015
End Date
November 1, 2018
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Nancy Gell

Assistant Professor

University of Vermont

Eligibility Criteria

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.

Outcomes

Primary Outcomes

Change from Baseline in Step counts

Time Frame: 8 weeks

Mean daily step counts as assessed by Actigraph Accelerometer

Change from Baseline in Moderate to Vigorous Physical Activity (MVPA)

Time Frame: 8 weeks

Weekly accumulated minutes spent in MVPA as assessed by Actigraph Accelerometer

Secondary Outcomes

  • Change from Baseline in Fatigue(8 weeks)
  • Change from Baseline in Self-regulation(8 weeks)
  • Change in Weekly average of mean daily step counts(8 weeks)
  • Change from Baseline in Self-efficacy to perform exercise(8 weeks)

Study Sites (1)

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