Telehealth Intervention for Improving Distress and Financial Toxicity in the Caregivers
Recruiting
N/A
Interventional Study
Hematopoietic and Lymphatic System Neoplasm
Malignant Solid Neoplasm
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Interventional
- Purpose
- Supportive Care
- Participants needed
- 50 (estimated)
- Sponsor
- Wake Forest University Health Sciences · Other
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About This Trial
This clinical trial assesses whether resource identification for primary caregivers can affect financial stress, quality of life, depression, and the general belief in the ability to cope with daily life. Caregivers of patients receiving cytoreductive surgery and hyperthermic intraperitoneal chemotherapy (CS+HIPEC) demonstrate that they endure high depressive symptom burdens and financial distress…
Trial Locations
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Eligibility Criteria
Inclusion Criteria
* Primary caregiver of a patient scheduled to receive CS+HIPEC at Atrium Health Wake Forest Baptist Comprehensive Cancer Center
* Access to a computer or smartphone and must have an email address
* 18 years of age or older at the time of consent
* The ability to understand and wi…
Contacts