Bemobile Intervention to Support Physical Activity in Cancer Survivors

University of Vermont

Status: Completed

Conditions: Cancer

Treatments: Behavioral: Bemobile

Study type: Interventional

Funder types: Other

Identifiers

NCT02824861

CHRMS15-405

VCC1504 (Other Identifier)

Details and patient eligibility

About

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.

Full 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.

Enrollment: 70 patients

Sex: All

Ages: 22+ years old

Volunteers: No Healthy Volunteers

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.

Trial design

Primary purpose: Supportive Care

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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70 participants in 2 patient groups

Text Intervention

Experimental group

Description:

Participants receive text messages to a personal cell phone over 8 weeks, wear a fitbit to monitor physical activity, and communicate with a health coach intermittently over 2 weeks

Treatment:

Behavioral: Bemobile

Active Control

Active Comparator group

Description:

Participants receive and wear a fitbit only for 8 weeks

Treatment:

Behavioral: Bemobile