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Improving Outcomes in Cancer Patients on Oral Anti-Cancer Medications Using a Multi-modal Mobile Health Intervention (CORA)

Primary Purpose

Renal Cell Cancer, Prostate Cancer, Effects of Chemotherapy

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
CORA- Device:smartphones"
Sponsored by
Massachusetts General Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Renal Cell Cancer

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:.

  • Adult (≥18 years) patients being treated at the Dana Farber Cancer Institute for Renal Cell Cancer or Prostate Cancer commencing a new course cycle of OAMs. . - -Participants must be ambulatory and able to consent for self.
  • Participants must have an Apple or Android smart phone and be willing to download the mobile application on their smartphones so they can utilize the intervention.
  • Patients must be able to read/speak English.

Exclusion Criteria:

  • Life expectancy less than 3 months as determined by the managing oncologist.
  • Significant psychiatric co-morbidities and memory or cognitive impairments. A significant psychiatric condition includes any condition which creates major distress for a patient or which markedly impairs the patient's daily functioning. It includes, but not limited to, acute psychoses, major depressive disorder, dementia, etc
  • Patients currently on similar interventional studies geared to improve medication adherence or in investigational drug trials in which adverse effects have not been fully elucidated.

Sites / Locations

  • Partners HealthCare Connected Health

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Intervention

Control

Arm Description

Download and use mobile health application - CORA- Device:smartphones for 12 weeks.

Usual Care - The control group will not use the study's mobile health application during the study.

Outcomes

Primary Outcome Measures

Change in Adherence to Oral Anti-Cancer Medications in patients with Renal Cell Cancer or Prostate Cancer on Oral Anti-Cancer Medications.
Medication adherence will be measured throughout the course of the study by the Medication Event Monitoring System. (Continuous data regarding medication adherence will be measured through this device and recorded in real time throughout the study - a period of 3 months.)

Secondary Outcome Measures

Severity of symptoms in patients on Oral AntiCancer Medications. (OAMs)
Symptom severity will be measured using the MD Anderson Symptom Severity Inventory.
Hospital utilization in patients on OAMs.
Hospital utilization to include number of visits to Emergency Department visits, urgent clinic visits and in-patient admissions.
Quality of life metrics in patients on OAMs.
The Functional Assessment of Cancer Therapy-General (FACT-G) is an instrument used to measure health-related quality of life. been used extensively worldwide. The FACT-G has four subscales: Physical Well-Being (PWB), Social/Family Well-Being (SWB), Emotional Well-Being (EWB), and Functional Well-Being (FWB).
patient engagement with the mobile-based intervention in patients on OAMs.
Data will be collected for the 12 week duration of the study from the mobile application on participants' patterns of use of application. Additionally, Closeout Survey will asses user experience using the study mobile application and will collect user feedback.
Severity of anxiety in patients on OAMS.
The Generalized Anxiety Disorder 7 Item Scale GAD-7 will be used to screen for and assess severity of generalized anxiety disorder in patients using OAMS. The GAD-7 is a self-administered 7 question instrument. It is a valid and efficient tool to screen for and asses the severity of generalized anxiety disorder. It is used in both clinical practice and research.
Severity of fatigue in patients on OAMs.
The Functional Assessment of Chronic Illness Therapy - Fatigue Version (FACIT-F) will be used to assess patient fatigue. It is a self administered 13 question instrument validated for use in chronic illness and frequently used with cancer patients.

Full Information

First Posted
December 24, 2014
Last Updated
August 29, 2020
Sponsor
Massachusetts General Hospital
Collaborators
McKesson Foundation, Dana-Farber Cancer Institute
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1. Study Identification

Unique Protocol Identification Number
NCT02375776
Brief Title
Improving Outcomes in Cancer Patients on Oral Anti-Cancer Medications Using a Multi-modal Mobile Health Intervention
Acronym
CORA
Official Title
Improving Outcomes in Cancer Patients on Oral Anti-Cancer Medications Using a Multi-modal mHealth Intervention
Study Type
Interventional

2. Study Status

Record Verification Date
August 2020
Overall Recruitment Status
Completed
Study Start Date
March 2015 (undefined)
Primary Completion Date
April 2018 (Actual)
Study Completion Date
December 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Massachusetts General Hospital
Collaborators
McKesson Foundation, Dana-Farber Cancer Institute

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This study evaluates a smart phone based mobile application designed for patients with Renal Cell and Prostate Cancer taking oral anti-cancer medications. (OAMs) All participants will be patients at the Dana Farber Cancer Institute in Boston, Massachusetts. Half of the participants will use the mobile application for a 3 month period along with their usual care. Half of the participants will just receive usual care. The investigators hope to show that cancer patients taking OAMs who use the mobile application will be better connected to their care team and will develop increased competency for self-care which will primarily increase medication adherence.
Detailed Description
The widespread and increasing use of oral anti-cancer medications (OAMs) has been ushered in by a rapidly increasing understanding of cancer pathophysiology. Furthermore, OAMs' popular ease of administration and potential cost savings has highlighted their central position in the healthcare system as a whole. Importantly, these facts have heightened appreciation of the unique challenges associated with OAMs use, especially in relation to prescribing, dispensing, reimbursement, education, adherence, and comprehensive quality and safety assurance. In this regard, the investigators goal is to improve medication adherence and clinical outcomes for cancer patients using OAMs through a mobile-enabled, multi-modal self-management and educational intervention . The intervention seeks to enable patients' self-efficacy to adhere to their medications through directed education and coaching, anticipation of symptoms and associated adverse events, and closer monitoring with accurate assessment of self-reported outcomes. This innovative approach necessarily includes personalizing feedback and management based on patients' own treatment regimen, baseline knowledge and elucidated barriers to adherence, and holds great promise in improving overall adherence, safety, and clinical outcomes in these patients. The investigators hypothesize that cancer patients on OAMs who use a mobile-based, multi-modal health self-management (M health) intervention designed for extensive patient education and symptom management will be better connected to their care team and will develop increased competency for self-care which will primarily increase medication adherence and improve secondary outcomes measured in this study compared to cancer patients on OAMs who do not use the mobile-based intervention.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Renal Cell Cancer, Prostate Cancer, Effects of Chemotherapy

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
84 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Intervention
Arm Type
Experimental
Arm Description
Download and use mobile health application - CORA- Device:smartphones for 12 weeks.
Arm Title
Control
Arm Type
No Intervention
Arm Description
Usual Care - The control group will not use the study's mobile health application during the study.
Intervention Type
Other
Intervention Name(s)
CORA- Device:smartphones"
Intervention Description
Participants will download and use Multi - modal mobile smartphone application (CORA -Device:smarthpones) designed for renal cell and prostate cancer patients taking anti-cancer medications
Primary Outcome Measure Information:
Title
Change in Adherence to Oral Anti-Cancer Medications in patients with Renal Cell Cancer or Prostate Cancer on Oral Anti-Cancer Medications.
Description
Medication adherence will be measured throughout the course of the study by the Medication Event Monitoring System. (Continuous data regarding medication adherence will be measured through this device and recorded in real time throughout the study - a period of 3 months.)
Time Frame
From randomization to end of study 12 weeks
Secondary Outcome Measure Information:
Title
Severity of symptoms in patients on Oral AntiCancer Medications. (OAMs)
Description
Symptom severity will be measured using the MD Anderson Symptom Severity Inventory.
Time Frame
From randomization to end of study 12 weeks
Title
Hospital utilization in patients on OAMs.
Description
Hospital utilization to include number of visits to Emergency Department visits, urgent clinic visits and in-patient admissions.
Time Frame
From randomization to end of study 12 weeks
Title
Quality of life metrics in patients on OAMs.
Description
The Functional Assessment of Cancer Therapy-General (FACT-G) is an instrument used to measure health-related quality of life. been used extensively worldwide. The FACT-G has four subscales: Physical Well-Being (PWB), Social/Family Well-Being (SWB), Emotional Well-Being (EWB), and Functional Well-Being (FWB).
Time Frame
From randomization to end of study 12 weeks
Title
patient engagement with the mobile-based intervention in patients on OAMs.
Description
Data will be collected for the 12 week duration of the study from the mobile application on participants' patterns of use of application. Additionally, Closeout Survey will asses user experience using the study mobile application and will collect user feedback.
Time Frame
From randomization to end of study 12 weeks
Title
Severity of anxiety in patients on OAMS.
Description
The Generalized Anxiety Disorder 7 Item Scale GAD-7 will be used to screen for and assess severity of generalized anxiety disorder in patients using OAMS. The GAD-7 is a self-administered 7 question instrument. It is a valid and efficient tool to screen for and asses the severity of generalized anxiety disorder. It is used in both clinical practice and research.
Time Frame
From randomization to end of study 12 weeks
Title
Severity of fatigue in patients on OAMs.
Description
The Functional Assessment of Chronic Illness Therapy - Fatigue Version (FACIT-F) will be used to assess patient fatigue. It is a self administered 13 question instrument validated for use in chronic illness and frequently used with cancer patients.
Time Frame
From randomization to end of study 12 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:. Adult (≥18 years) patients being treated at the Dana Farber Cancer Institute for Renal Cell Cancer or Prostate Cancer commencing a new course cycle of OAMs. . - -Participants must be ambulatory and able to consent for self. Participants must have an Apple or Android smart phone and be willing to download the mobile application on their smartphones so they can utilize the intervention. Patients must be able to read/speak English. Exclusion Criteria: Life expectancy less than 3 months as determined by the managing oncologist. Significant psychiatric co-morbidities and memory or cognitive impairments. A significant psychiatric condition includes any condition which creates major distress for a patient or which markedly impairs the patient's daily functioning. It includes, but not limited to, acute psychoses, major depressive disorder, dementia, etc Patients currently on similar interventional studies geared to improve medication adherence or in investigational drug trials in which adverse effects have not been fully elucidated.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kamal Jethwani, MD, MPH
Organizational Affiliation
Center for Connected Health, Partners HealthCare
Official's Role
Principal Investigator
Facility Information:
Facility Name
Partners HealthCare Connected Health
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02114
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
Undecided

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Improving Outcomes in Cancer Patients on Oral Anti-Cancer Medications Using a Multi-modal Mobile Health Intervention

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