Breast Cancer, Head and Neck Cancer, Lung Cancer, Prostate Cancer
Conditions
Brief summary
The goal of this study is to measure the effect of radiation therapy on the activity levels of patients. This will be achieved by tracking their activity levels during a treatment course of radiation therapy.
Detailed description
At the University of Pittsburgh (UPMC) St. Margaret and UPMC Shadyside, in the department of radiation oncology, breast, prostate, head and neck, and lung cancer patients will receive the standard treatment for their cancer and in no way will this study interfere with this treatment. Prior to initiation of radiation, consenting patients will be given Misfit activity tracking devices (accelerometers) to be worn on their wrist to track their activity levels throughout the course radiation therapy. Bracelets will be given to patients by the PI or co-investigators (MDs involved in patient's care) at date of consent and returned at completion of the study. The bracelets will track daily steps taken, calories burned, miles walked, and restful and restless sleep. Again, the purpose of the study is merely to measure the affect radiation therapy has on activity levels of patients.
Interventions
None listed
Sponsors
Study design
Eligibility
Inclusion criteria
* Diagnosis of Breast, Prostate, Lung or Head and Neck Cancer * Eastern Cooperative Oncology Group (ECOG) performance status of 0-1 * Ability to walk 100 feet without rest * Signed informed consent
Exclusion criteria
* Any other noncutaneous cancer diagnosis under active treatment * Known metastatic disease
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Activity level | up to 15 weeks | Misfit activity tracking devices (accelerometers) will be worn by patients to track their activity levels 1 day to 4 weeks before radiotherapy, during radiotherapy, and for 1 day to 4 weeks after radiotherapy. |
Countries
United States