Clinical Trial 21751

Cancer Type: Healthy Subjects
Study Type: Supportive Care
NCT#: NCT05379933

Phase: N/A
Principal Investigator: Gonzalez, Brian

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Overview

Study Title

C-PRIME: Caregiver Protocol for Remotely Improving, Monitoring, and Extending Quality of Life

Summary

Objective

The long-term goal of this research is to promote family caregiver (FCG) health and well-being. The central hypothesis is that by offering tools for self-monitoring self-care and health behaviors, as well as coaching to identify goals and problem-solve how to achieve them, we will encourage FCGs to engage in more self-care and health behaviors, which ultimately will improve FCG well-being. The aims of this proposal are to: Aim 1. Determine the feasibility and acceptability of C-PRIME in the outpatient oncology setting. Aim 2. Determine the preliminary efficacy of C-PRIME in the outpatient oncology setting.

Treatments

Therapies

Medications

Inclusion Criteria

Eligible FCG participants will be:

An unpaid family member or friend who provides assistance and support with healthcare of a non-institutionalized patient receiving some form of treatment for stage III or IV colorectal cancer at Moffitt Cancer Center

Age 18+ years

English or Spanish speaking

Able to complete questionnaires and engage in short discussions with coaches

Able to identify a primary care medical provider

Willing/able to use a mobile device provided by the study team or their own their device.

Eligible patient participants will be:

Patients scheduled to begin receiving or receiving treatment for stage III or IV colorectal cancer at Moffitt Cancer Center

Age 18+ years

English or Spanish Speaking

Able to nominate one or more primary caregiver

Exclusion Criteria

Participants who do not meet the study inclusion criteria

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