The HealthScore Health Coaching Program (NCT04923997) | Clinical Trial Compass
CompletedNot Applicable
The HealthScore Health Coaching Program
United States140 participantsStarted 2020-05-11
Plain-language summary
Purpose: The HealthScore Health Coaching Program aims to deliver 6-months of 1:1 home-based health coaching to cancer patients receiving treatment and survivors of any diagnosis at UNC Cancer Hospital. This study hopes to preserve physical function, address unmet physical, nutritional, psychological, social and other needs.
Procedures: This will be done through individualized health coaching, weekly symptom survey administration, monthly supportive care questionnaires, and physical assessments at baseline, 3 months and 6 months.
Participants: All cancer patients with appointments at UNC Cancer Hospitals.
Who can participate
Age range15 Years
SexALL
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Inclusion Criteria:
* Patients must have an appointment at a cancer center, including if they are an inpatient, if they are seen by a clinical service providing care to patients with cancer or sickle cell disease, and if they are \> age 15. They can be receiving active treatment or in survivorship, with no restrictions based on time since the conclusion of active treatment. No exclusions will be made based on gender, ethnicity or race.
* Patient must be willing and able to participate in a 6-month intervention.
* Patients must be willing and able to provide patient-reported survey responses electronically or by telephone.
* Patients must have the ability to use a wearable sensor and view wearable sensor data at home.
* Patients must have a working email address and have the ability to check and respond to email.
* Participation in a research study is allowable by the patient's insurance provider
Exclusion Criteria:
* Patients who do not read and speak English, as program software has not been translated into other languages at this time.
* The patient has concurrent medical or psychiatric conditions that may preclude participation (i.e. moderate to severe dementia, uncontrolled schizophrenia, or other conditions that would render them unable to provide informed consent or complete questionnaires).