PROStep: A Feasibility Trial Using PROs and Step Data to Monitor Patients With Lung and GI Cancers
- Conditions
- Lung CancerGastro-intestinalCancer
- Interventions
- Other: PRO questionnaireOther: Step monitoringOther: PROStep Dashboard (clinicians)Other: Active nudge text feedback
- Registration Number
- NCT04616768
- Lead Sponsor
- Abramson Cancer Center at Penn Medicine
- Brief Summary
Telemedicine allows clinicians to utilize modern telecommunication technology to provide healthcare services to patients including remote symptom monitoring. Given the spread of COVID-19 both locally and globally, is crucial to adapt accordingly in order to safely provide vulnerable cancer patient populations with optimal care while minimizing risk of exposure to COVID-19. In this study, the investigators will utilize remote monitoring of patients with cancer via weekly patient-reported outcome (PRO) collection through the Way to Health (W2H) smartphone application and step data through wearable Fitbit devices. Patients with incurable lung and gastrointestinal cancers will be recruited based on whether they receive their care in-clinic or remotely. They will respond to weekly phone-based symptom surveys and wear Fitbits that track step data. This data will be collated in a Palliative Care Assessment Dashboard (PROStep Dashboard) sent to clinicians prior to each oncology visit to help inform patient management. In this feasibility study, two arms of patients will be monitored with symptom surveys and Fitbits; the study will randomize these patients to either 1) receive text feedback or 2) receive no text feedback. A third arm of patients will be randomized to receive no feedback, symptom surveys, or Fitbit device. Clinicians for patients in each arm will receive the PROstep Dashboard. The study will determine feasibility of this monitoring approach, and compare patient adherence to symptom surveys and step data collection between the two intervention arms.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 109
- English-speaking
- Have a diagnosis of incurable or Stage IV lung or gastrointestinal cancer
- Receive primary oncology care with a thoracic or gastrointestinal medical oncology specialist at the Perelman Center for Advanced Medicine (i.e. does not have a local oncologist that provides cancer care, including other UPHS clinic sites)
- Currently receiving or planned receipt within 2 weeks of IV chemotherapy (see exclusions below)
- The patient has a smart phone that can receive SMS text messages and has blue-tooth capability that can connect to Fitbit.
- Age < 18 years
- Patients has used a wheelchair, been bedbound or is unable to walk without assistance from other people every day for the past 7 days (patients are not excluded for the use of walkers or canes)
- Patients who are receiving checkpoint inhibitor monotherapy or oral tyrosine kinase inhibitors
- Patients who receive chemotherapy infusions at another UPHS site or outside of UPHS or whose primary oncologist is not in thoracic or gastrointestinal oncology groups at PCAM. Notably, patients who receive part of their chemotherapy regimen at home will still be allowed to enroll.
- Lung cancer patients enrolled in an ongoing palliative care clinical trial that may lead to better communication regarding symptoms and functional status.
- Clinician concerns about behavioral health issues that may prevent engagement with text message prompts
- Are enrolled in another interventional clinical trial (as clinical trials often have a substantial symptom-reporting structure; non-interventional clinical trials are permitted e.g. trials that just involve blood tests)
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Arm B - Intervention without text feedback PRO questionnaire An arm of ≤42 patients enrolled intervention patients will be randomized to receive weekly patient-reported outcome questionnaires, be given Fitbits to monitor weekly step counts and utility surveys at 3 and 6 months following enrollment. Their clinicians will receive a "PROStep Dashboard" prior to their appointments and utility surveys at 3 and 6 months. Arm B - Intervention without text feedback Step monitoring An arm of ≤42 patients enrolled intervention patients will be randomized to receive weekly patient-reported outcome questionnaires, be given Fitbits to monitor weekly step counts and utility surveys at 3 and 6 months following enrollment. Their clinicians will receive a "PROStep Dashboard" prior to their appointments and utility surveys at 3 and 6 months. Arm B - Intervention without text feedback PROStep Dashboard (clinicians) An arm of ≤42 patients enrolled intervention patients will be randomized to receive weekly patient-reported outcome questionnaires, be given Fitbits to monitor weekly step counts and utility surveys at 3 and 6 months following enrollment. Their clinicians will receive a "PROStep Dashboard" prior to their appointments and utility surveys at 3 and 6 months. Arm C - Intervention with text feedback PRO questionnaire An arm of ≤42 patients enrolled intervention patients will be randomized to receive weekly patient-reported outcome questionnaires, be given Fitbits to monitor weekly step counts and utility surveys at 3 and 6 months following enrollment. Their clinicians will receive a "PROStep Dashboard" prior to their appointments and utility surveys at 3 and 6 months. Patients in this arm will receive an additional text prior to appointments that summarizes their symptoms and incorporates an active nudge question. Arm C - Intervention with text feedback Step monitoring An arm of ≤42 patients enrolled intervention patients will be randomized to receive weekly patient-reported outcome questionnaires, be given Fitbits to monitor weekly step counts and utility surveys at 3 and 6 months following enrollment. Their clinicians will receive a "PROStep Dashboard" prior to their appointments and utility surveys at 3 and 6 months. Patients in this arm will receive an additional text prior to appointments that summarizes their symptoms and incorporates an active nudge question. Arm C - Intervention with text feedback Active nudge text feedback An arm of ≤42 patients enrolled intervention patients will be randomized to receive weekly patient-reported outcome questionnaires, be given Fitbits to monitor weekly step counts and utility surveys at 3 and 6 months following enrollment. Their clinicians will receive a "PROStep Dashboard" prior to their appointments and utility surveys at 3 and 6 months. Patients in this arm will receive an additional text prior to appointments that summarizes their symptoms and incorporates an active nudge question. Arm C - Intervention with text feedback PROStep Dashboard (clinicians) An arm of ≤42 patients enrolled intervention patients will be randomized to receive weekly patient-reported outcome questionnaires, be given Fitbits to monitor weekly step counts and utility surveys at 3 and 6 months following enrollment. Their clinicians will receive a "PROStep Dashboard" prior to their appointments and utility surveys at 3 and 6 months. Patients in this arm will receive an additional text prior to appointments that summarizes their symptoms and incorporates an active nudge question.
- Primary Outcome Measures
Name Time Method Patient perceptions of symptom management These will be measured at 6 months after enrollment for each patient (or 3 months if the patient did not complete their 6 month survey) Patient utility surveys will use a 5-point Likert scale for responses scored 1-5. The two co-primary outcomes will compare the scores for the following two questions, measured at 6 months (or 3 months if the patient did not complete their 6 month survey), between intervention patients (Arms B + C) and control patients (Arm A).
The two co-primary outcomes will compare the scores for the following two questions:
* How well do you feel your oncology team understands your symptoms (e.g. nausea, vomiting, weight loss, etc.)? (1-5)
* How well do you feel your oncology team understands your activity level and ability to function? (1-5)
Likert scale responses are defined as: 1 = Not at all; 2 = Slightly; 3 = Moderately; 4 = Considerably; 5 = Completely.
- Secondary Outcome Measures
Name Time Method Additional analysis of the primary outcome between arms These will be measured at 3 months after enrollment for each patient. The following secondary outcome will compare the same questions measured at 3 months, between intervention patients (Arms B + C) and control patients (Arm A).
* How well do you feel your oncology team understands your symptoms (e.g. nausea, vomiting, weight loss, etc.)? (1-5)
* How well do you feel your oncology team understands your activity level and ability to function? (1-5)
Likert scale responses are defined as: 1 = Not at all; 2 = Slightly; 3 = Moderately; 4 = Considerably; 5 = Completely.Adherence Each patient will be enrolled in the trial for a total of six months. We will compare cumulative adherence for patients in the intervention group (arm B and arm C). Each week, adherence will be defined as each week where the patient submits the weekly survey (i.e. adherence to PRO) and has step data for 4 of 7 days of the week (i.e. adherence to Fitbit platform), divided by the total number of weeks that the patient is enrolled in the trial.
* Comparison of mean patient adherence at three months for patients in arm B vs arm C
* Comparison of mean patient adherence at six months for patients in arm B vs arm CFitbit step data Each patient will be enrolled in the trial for a total of six months. We will analyze trends in the Fitbit step data.
Comparison of PRO scores between patients in arm B vs. arm C. Fitbit step data will be measured using mean daily step counts for all days in which Fitbit data is collected. Days where the patient does not have Fitbit data will be excluded from these calculations.Comparison of PRO scores (Arms B and C) Each patient will be enrolled in the trial for a total of six months. These will be measured using mean and median composite symptom scores reported by patients. The composite score is the sum of the scores for each domain in the PRO survey (0-32). The mean or median composite symptom score is the mean or median of all composite scores collected during the study. The PRO surveys use a 5-point scale (0 as LESS (None) to 4 as MORE (Very severe)).
1. In the last 7 days, how OFTEN did you have NAUSEA??
2. In the last 7 days, how OFTEN did you have LOOSE OR WATERY STOOLS (DIARRHEA/DIARRHOEA)??
3. In the last 7 days, what was the SEVERITY of your CONSTIPATION at its WORST?
4. In the last 7 days, what was the SEVERITY of your PAIN at its WORST?
5. In the last 7 days, how much did your SHORTNESS OF BREATH INTERFERE with your usual or daily activities?
6. In the last 7 days, how OFTEN did you have SAD OR UNHAPPY FEELINGS?
7. In the last 7 days, how OFTEN did you feel ANXIETY?
8. Over the past week I would generally rate my activity as:
Trial Locations
- Locations (1)
Perelman Center for Advanced Medicine (PCAM)
🇺🇸Philadelphia, Pennsylvania, United States