Association Between Health Care Provider (HCP)-Assessed ECOG Performance Status (PS) and Overall Survival, and Objectively Measure of Physical Activity (PA) Levels in Advance-cancer Patients"
Last updated on July 2021Recruitment
- Recruitment Status
- Recruiting
- Estimated Enrollment
- 70
Summary
- Conditions
- Metastatic Malignant Neoplasm in the Neck
- Metastatic or Locally Unresectable Solid Tumor
- Malignant Head and Neck Neoplasm
- Stage IVA Major Salivary Gland Cancer AJCC v7
- Stage I Nasopharyngeal Carcinoma AJCC v7
- Stage I Oropharyngeal Carcinoma AJCC v6 and v7
- Stage II Major Salivary Gland Cancer AJCC v7
- Stage II Oropharyngeal Carcinoma AJCC v6 and v7
- Stage IIC Colorectal Cancer AJCC v7
- Stage IVA Oral Cavity Cancer AJCC v6 and v7
- Malignant Neoplasm
- Metastatic Malignant Neoplasm in the Uterine Cervix
- Stage IVB Hypopharyngeal Carcinoma AJCC v7
- Stage II Oral Cavity Cancer AJCC v6 and v7
- Stage IVB Oropharyngeal Carcinoma AJCC v7
- Stage IVA Laryngeal Cancer AJCC v7
- Stage IVA Nasopharyngeal Carcinoma AJCC v7
- Stage IVB Major Salivary Gland Cancer AJCC v7
- Stage IV Colorectal Cancer AJCC v7
- Pancreatic Adenocarcinoma
- Stage III Laryngeal Cancer AJCC v6 and v7
- Stage IVB Nasopharyngeal Carcinoma AJCC v7
- Stage III Oral Cavity Cancer AJCC v6 and v7
- Stage I Oral Cavity Cancer AJCC v6 and v7
- Stage II Colorectal Cancer AJCC v7
- Stage IIB Colorectal Cancer AJCC v7
- Stage IIIB Colorectal Cancer AJCC v7
- Stage IIA Colorectal Cancer AJCC v7
- Stage IVA Colorectal Cancer AJCC v7
- Pancreatic Neuroendocrine Carcinoma
- Stage II Nasopharyngeal Carcinoma AJCC v7
- Stage IVB Oral Cavity Cancer AJCC v6 and v7
- Recurrent Colorectal Carcinoma
- Stage III Colorectal Cancer AJCC v7
- Stage III Oropharyngeal Carcinoma AJCC v7
- Stage IVA Oropharyngeal Carcinoma AJCC v7
- Stage III Hypopharyngeal Carcinoma AJCC v7
- Stage I Colorectal Cancer AJCC v6 and v7
- Stage I Hypopharyngeal Carcinoma AJCC v7
- Stage I Major Salivary Gland Cancer AJCC v7
- Stage IVB Colorectal Cancer AJCC v7
- Stage IVB Laryngeal Cancer AJCC v7
- Stage IVA Hypopharyngeal Carcinoma AJCC v7
- Stage IIIA Colorectal Cancer AJCC v7
- Stage IIIC Colorectal Cancer AJCC v7
- Stage III Major Salivary Gland Cancer AJCC v7
- Stage III Nasopharyngeal Carcinoma AJCC v7
- Stage II Hypopharyngeal Carcinoma AJCC v6 and v7
- Type
- Interventional
- Phase
- Not Applicable
- Design
- Allocation: Non-RandomizedIntervention Model: Parallel AssignmentMasking: None (Open Label)Primary Purpose: Health Services Research
Participation Requirements
- Age
- Between 18 years and 125 years
- Gender
- Both males and females
Description
PRIMARY OBJECTIVES: I. To explore the feasibility and acceptability in diverse samples of cancer patients of wireless collection and transmission of data for transfer into the open-source cyberinfrastructure (CI) called Cyberinfrastructure for Comparative Effectiveness Research (CYCORE). OUTLINE: Pa...
PRIMARY OBJECTIVES: I. To explore the feasibility and acceptability in diverse samples of cancer patients of wireless collection and transmission of data for transfer into the open-source cyberinfrastructure (CI) called Cyberinfrastructure for Comparative Effectiveness Research (CYCORE). OUTLINE: Patients are assigned to 1 of 4 arms. ARM I (COLORECTAL CANCER PATIENTS) (CLOSED TO ACCRUAL AS OF 01/30/14): Patients use two accelerometers, a blood pressure monitor, a heart rate monitor, a global positioning system (GPS) device, and a smart phone that prompts patients to electronically answer questions about exercise and health-related symptoms and feelings. The devices are used for 5 consecutive days. After a 2 week period, patients resume use of the devices for an additional 5 days. ARM II (HEAD AND NECK CANCER PATIENTS) (CLOSED TO ACCRUAL AS OF 01/30/14): Patients use two accelerometers, a blood pressure monitor, a weight scale, and a smart phone that prompts patients to electronically answer questions about diet and health-related symptoms. The devices are used for 5 consecutive days. After a 2 week period, patients resume use of the devices for an additional 5 days. ARM III (HEAD AND NECK CANCER PATIENTS) (CLOSED TO ACCRUAL AS OF 01/30/14): Patients use a smart phone that prompts patients to electronically answer questions about diet, health-related symptoms, and swallowing exercises. Patients also take video recordings of their neck while performing swallowing exercises. The device is used for 5 consecutive days. After a 2 week period, patients resume use of the device for an additional 5 days. ARM IV (CANCER SURVIVORS THAT ARE CURRENT/FORMER SMOKERS) (CLOSED TO ACCRUAL AS OF 01/30/14): Patients use a carbon monoxide (CO) monitor and a smart phone that prompts patients to electronically answer questions about smoking. Patients also take video recordings of themselves while exhaling into the CO monitor. The devices are used for 5 consecutive days. After a 2 week period, patients resume use of the devices for an additional 5 days. PANCREATIC CANCER STUDY (PCS): Patients receive post-surgical wellness program consisting of physical activity, nutrition counseling, and daily monitoring (physical activity, weight, and self-reported data) for up to 7 months post-op. Technological Approach to Performance Status (TAPS) Study: Patients use two Physical Activity monitor devices, the wrist-worn device (Fitbit) continuously and the Actigraph during waking hours. Patients use the devices for 7 consecutive days.
Tracking Information
- NCT #
- NCT01365169
- Collaborators
- National Cancer Institute (NCI)
- Investigators
- Principal Investigator: Susan K Peterson M.D. Anderson Cancer Center