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Facilitating Physical Activity Behavior and Health Outcomes in Breast Cancer Patients Receiving Chemotherapy

Phase 2
Conditions
Breast Cancer
Interventions
Behavioral: Physical Activity Resource Kit
Behavioral: Standard Materials
Registration Number
NCT01053468
Lead Sponsor
Athabasca University
Brief Summary

Breast cancer and its treatments can take a toll on the physical and psychosocial well-being of cancer survivors. Few interventions can help breast cancer patients improve their physical strength, stamina, and overall well-being. Developing ways to facilitate PA behavior during chemotherapy for breast cancer are necessary. This trial explores ways that breast cancer patients receiving chemotherapy can learn about and engage in PA during chemotherapy. This trial will also give Southern Alberta breast cancer survivors an opportunity to participate in evidence-based programs designed to facilitate their health, breast cancer recovery, and disease-free survival.

The investigators primary hypothesis is that women receiving the PA intervention resource kit will report a more positive change in self-reported PA at the end of chemotherapy treatments when compared to the group receiving standard materials.

Detailed Description

Primary Objective:

To compare the effects of an evidence-based intervention consisting of targeted breast-cancer specific PA print materials (i.e., Exercise for health), a step pedometer, a step-walking guidebook (i.e., Step into survivorship), and a physical activity and step journal (INT) to a comparison group receiving a generic, two-page public health PA resource (Standard Material: SM).

Recruitment & Eligibility

Status
UNKNOWN
Sex
Female
Target Recruitment
150
Inclusion Criteria
  • are diagnosed with stage I -IIIA breast cancer
  • are scheduled to receive neoadjuvant or adjuvant chemotherapy
  • did not receive transabdominal rectus abdominus muscle (TRAM) reconstructive surgery
  • are >18 years of age
  • receive approval from their treating oncologist to participate
  • do not have uncontrolled hypertension, cardiac illness, or psychiatric conditions (i.e., indicated in patient medical charts).
Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
PA Behavior InterventionPhysical Activity Resource KitPhysical Activity Resource Kit
Standard MaterialsStandard MaterialsReceive physical activity handout from the Canadian Public Health Agency
Primary Outcome Measures
NameTimeMethod
Self-reported physical activityBaseline, post intervention, 6 months follow up
Secondary Outcome Measures
NameTimeMethod
Cancer specific health related quality of lifeBaseline, post intervention, 6 months follow up
Psychosocial health outcomesBaseline, post intervention, 6 months follow up
Objective step counts (pedometer)Baseline, post intervention, 6 months follow up
Chemotherapy completion rateBaseline, post intervention, 6 months follow up
Determinants of physical activityBaseline, post intervention, 6 months follow up
Physical functioningBaseline, post intervention, 6 months follow up

Trial Locations

Locations (5)

Medicine Hat Cancer Centre

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Medicine Hat, Alberta, Canada

Tom Baker Cancer Centre

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Calgary, Alberta, Canada

Grande Prairie Cancer Centre

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Grande Prairie, Alberta, Canada

Lethbridge Cancer Centre

πŸ‡¨πŸ‡¦

Lethbridge, Alberta, Canada

Central Alberta Cancer Centre

πŸ‡¨πŸ‡¦

Red Deer, Alberta, Canada

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