Non-small Cell Lung Cancer
Conditions
Brief summary
Symptoms are common among patients with advanced malignancy undergoing treatment, and yet often go unrecognized by treatment providers. In addition to contributing to morbidity, poorly controlled symptoms drive emergency room utilization and hospital admission in this population, representing significant cost to patients, families, and the health care system. Systematic collection of patient-reported outcomes (PROs) has been proposed as a way to arm providers with the information necessary to intervene early, intensify symptom management, and improve symptom control. Recent research suggests that a standardized, web-based program of weekly patient-reported symptom monitoring leads to improved health-related quality of life and reduced acute care utilization; it may also prolong overall survival. Despite mounting evidence supporting its use among oncology patients, systematic PRO collection is lacking at most cancer centers, and optimal models for collection of PROs are poorly understood. The objective of this study is to evaluate prospectively the feasibility of a novel mobile phone-based intervention of weekly symptom reporting, among patients undergoing treatment for advanced non-small cell lung cancer.
Interventions
OTHERa novel mobile phone-based intervention for automated electronic PRO collection
Over the three-month study period, patients will be prompted weekly via text message to self-report up to eleven common symptoms, as well as their performance status and quality of life.
Sponsors
Abramson Cancer Center at Penn Medicine
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Adult patient (age ≥ 18 years) with advanced (metastatic) non-small cell lung cancer, initiating a new line of palliative-intent treatment at Abramson Cancer Center * Ability to read and respond to questions in English * Ability to provide informed consent to participate in the study * Access to a smart phone capable of SMS-text messaging and internet access
Exclusion criteria
* Inability to read and respond to questions in English * Inability or unwillingness to provide informed consent to participate in the study * Inability to engage with SMS-text based platform * Current enrollment in a clinical trial
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Number of subjects who will adhere to the mobile phone-based intervention | 3 months | evaluate subjects to study-level adherence of a mobile phone-based intervention for automated PRO collection |
Countries
United States
Outcome results
None listed