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Feasibility of Integrating the Outcomes4Me Smartphone Navigation Application Into the Care Management of Breast Cancer Patients

Feasibility of Integrating the Outcomes4Me Smartphone Navigation Application Into the Care Management of Breast Cancer Patients

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04262518
Acronym
FIONA
Enrollment
125
Registered
2020-02-10
Start date
2020-06-01
Completion date
2020-10-31
Last updated
2020-06-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breast Cancer, Breast Carcinoma, Invasive Breast Cancer, Metastatic Breast Cancer, Metastatic Breast Carcinoma

Keywords

Invasive Breast Cancer, Metastatic Breast Cancer, NCCN Guidelines, Patient Navigation, Treatment Options, Clinical Trial Options, Symptom Management

Brief summary

This study aims to investigate the role of a mobile health app, Outcomes4Me, in the navigation of care for people with breast cancer.

Detailed description

This protocol is a single arm pilot study of a novel breast cancer navigation app that is intended to assist patients with breast cancer understand their diagnosis and treatment options (both as part of standard of care practice and clinical trials) and manage their care, through treatment and symptom tracking. Patients will also be able to share information and get news via the app relevant to their cancer subtype. Results from this intervention will inform future clinical integration efforts, improve patient-centeredness of such an app-based health content and data platform, and inform the design of a larger, randomized study to demonstrate an improvement in patients' outcomes as well as enhanced Real-World Evidence (RWE) data collection.

Interventions

DEVICEOutcomes4Me Mobile App

A mobile app that provides patient navigation and treatment and clinical trial options to people with breast cancer

Sponsors

Massachusetts General Hospital
CollaboratorOTHER
Outcomes4Me
Lead SponsorINDUSTRY

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* 18 years or older, with histologically or cytologically confirmed invasive breast cancer stage I-IV * Must be on, or planning to be on within 4 weeks of registration, active therapy, with the intent to receive some element of active therapy \> 28 days after registration * Must be able to understand, read, and write in English and be able to sign informed consent * Must have an Apple or Android smart phone that they are able to use and download the Outcomes4Me app on * Must have the ability to access the internet at least once per week via their smart phone (having a computer is not required)

Exclusion criteria

* Participations seen for consultation opinion only and are not planning to receive some element of active treatment from an MGH medical or radiation oncology provider at MGH (Boston or Waltham sites) during the 12-week study period

Design outcomes

Primary

MeasureTime frameDescription
Measure # of times a patient logs into the Outcomes4Me app over a 12 week period12 WeeksWe will track engagement with the app by tracking the number of times a user logs in to the Outcomes4Me app over a 12 week period. The app will be considered feasible if at least 40% of enrolled patients engage with the Outcomes4Me app at least 3 times during the 12-week study period.

Secondary

MeasureTime frameDescription
Measure System-Usability Score (SUS) of app usage12 weeksUsability will be assessed using the System Usability Scale (SUS). We wil collect the input of breast cancer patients to the SUS questions, using in-app surveys and will calculate the SUS score. We will assess overall satisfaction with the app by asking users to provide an answer to the question How likely are you to recommend this product to a friend on a scale of 0-10.
Measure Net-Promoter Score (NPS) of app usage12 weeks

Countries

United States

Contacts

Primary ContactAmanda Stroiney
amanda@outcomes4me.com860-916-4075
Backup ContactMaya Said, Sci.D
617-794-4963

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 15, 2026