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Spots Global Cancer Trial Database for Comprehensive Patient Reported Outcomes (PRO) Management for Oncology Practice

The following info and data is provided "as is" to help patients around the globe.
We do not endorse or review these studies in any way.

Trial Identification

Brief Title: Comprehensive Patient Reported Outcomes (PRO) Management for Oncology Practice

Official Title: Phase II Study of Comprehensive Patient Reported Outcomes (PRO) Management for Oncology Practice

Study ID: NCT01108315

Conditions

Breast Cancer

Study Description

Brief Summary: Cancer symptoms due to disease progression or side effects caused by cancer treatment are prevalent. Most cancer patients are treated in outpatient settings. Patients may be provided with patient education materials and counseled on anticipated side effects while being provided with different self-management options and warnings regarding when medical care is required. Despite these efforts, many people feel set adrift in having to self-manage treatment and illness related symptoms at home resulting in a sense of burden for the patient and the caregiver. When the patient does visit the doctor, they increasingly are asked questions to elicit information about symptoms and performance using structured questionnaires that are shown to give reproducible, meaningful, quantitative assessments of how patients feel and how they function-measures that are called patient reported outcomes or PROs. The questionnaires used to collect this information are called PRO instruments. The use of PRO instruments is part of a general movement toward the idea that the patient, properly queried, is the best source of information about how he or she feels. The goal of using PRO measures is to provide better information to doctors and patients so that the best treatment for patients can be determined. PURPOSE: To reduce the isolation of patients/caregivers from the medical care team and to improve patient/provider communication and clinical decisions by keeping documented daily reports of patient symptoms online, having notifications sent to the medical team of moderate to severe symptoms and by reviewing these reports at clinic visits with the medical staff.

Detailed Description:

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: FEMALE

Healthy Volunteers: No

Locations

Arizona Cancer Center, Tucson, Arizona, United States

Seattle Cancer Care Alliance, Seattle, Washington, United States

Contact Details

Name: DerShung Yang, PhD

Affiliation: BrightOutcome

Role: PRINCIPAL_INVESTIGATOR

Name: VK Gadi, MD

Affiliation: University of Washington

Role: PRINCIPAL_INVESTIGATOR

Name: Ana Maria Lopez, MD

Affiliation: University of Arizona

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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