Telehealth Intervention for Improving Distress and Financial Toxicity in the Caregivers
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About
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. Further, they experience symptom trajectories that differ from those of patients. In short, they require differential timing of supportive interventions. This study aims to reduce financial toxicity and distress levels and to increase self-efficacy, satisfaction and engagement with care. Information gathered from this study may help researchers determine whether telehealth interventions for caregivers may increase awareness of recommended resources that could be beneficial during caregivers journey.
Full description
PRIMARY OBJECTIVE:
I. To assess the feasibility of a telehealth navigation intervention for CS+HIPEC caregivers.
SECONDARY OBJECTIVES:
I. To assess the efficacy of the intervention on financial distress and depression in intervention and standard of care caregivers.
II. To compare financial distress in intervention caregivers as compared to standard of care caregivers.
III. To compare satisfaction with care experiences in intervention caregivers as compared to standard of care caregivers.
IV. To compare self-efficacy for navigating treatment-related costs in intervention caregivers as compared to standard of care participants.
V. To compare self-reported community resource use among intervention and standard of care caregivers.
VI. To compare the quality of life over time in intervention caregivers as compared to standard of care caregivers.
VII. To compare social support over time in intervention caregivers as compared to standard of care caregivers.
VIII. To compare treatment satisfaction for intervention caregivers as compared to standard of care caregivers.
OUTLINE: Participants are randomized to 1 of 2 groups.
GROUP I: Participants receive telehealth navigation intervention which may consist of referral to specific resources for caregiving experience over 1 hour 1-4 weeks prior to patient's surgery.
GROUP II: Participants receive standard caregiving experience on study.
After completion of study intervention, participants are followed up at 3, 6, 12, and 24 months.
Enrollment
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Inclusion and exclusion 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 willingness to provide written informed consent
- The ability to read and write English
Exclusion Criteria
- Patient declines access to their medical record
Trial design
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Interventional model
Masking
50 participants in 2 patient groups
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Central trial contact
Study Coordinator
Data sourced from clinicaltrials.gov
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