No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
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At a Glance
Age
18 – 99
Sex
Any
Study type
Interventional
Purpose
Supportive Care
Participants needed
162 (estimated)
Sponsor
UNC Lineberger Comprehensive Cancer Center · Other
Who this trial is looking for
This trial is looking for caregivers of adults with cancer and diabetes to participate in a support program. Participants will help improve support services for caregivers through a coaching program.
Are You a Good Fit for This Trial?
You may be able to join if
I speak English.
I am at least 18 years old.
I can give my written or verbal consent to participate.
I am an informal (unpaid) caregiver for an adult with stage II-IV cancer and diabetes.
You may not be able to join if
I cannot read or speak English.
I have another serious illness that prevents my participation.
I was part of the development phase of this intervention.
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer three quick questions written from this study's own rules to see if you may qualify. No account needed to find out.
This study investigates the feasibility, acceptability, and preliminary efficacy of enCompass Humana, a social support intervention for caregivers of patients with cancer and diabetes. The enCompass program aims to improve support for these caregivers through a randomized feasibility study of a pilot-tested coaching and navigation program.
Caregiver services and system-level support are essential…
This study investigates the feasibility, acceptability, and preliminary efficacy of enCompass Humana, a social support intervention for caregivers of patients with cancer and diabetes. The enCompass program aims to improve support for these caregivers through a randomized feasibility study of a pilot-tested coaching and navigation program.
Caregiver services and system-level support are essential, but successful interventions for cancer caregivers are rarely standardized or systematically disseminated. Consequently, many programs do not reach the most underserved caregivers. Challenges to implementation include substantial clinical staff involvement, lack of dissemination and implementation information, and failure to tailor interventions to rural contexts. Despite the lack of standardized supportive interventions, national reports and legislative efforts increasingly recognize the need to support caregivers.
Caregivers reported unmet needs in all domains of social support, including instrumental help (e.g., in-home help, housekeeping), logistical and coordination support (e.g., food delivery, accompanying patients to appointments), information about illness and progression, emotional support, self-care guidance, and financial assistance (e.g., parking costs, lost wages). Caregivers show high interest in services but cited uncertainty and lack of strategies for accessing resources. Many are unaware of existing services. Interviews with oncology clinicians and healthcare administrators revealed similar findings: resources exist, but there is no system to match them with caregivers' needs.
Preliminary data suggest the intervention improves caregiver coping self-efficacy and reduces anxiety and depression in patients. With input from stakeholders, including caregivers, patients, family caregiving experts, and clinical care experts, the study team adapted the CARING application into enCompass to mitigate structural barriers and normalize support-seeking. The long-term goal is to adapt this psychosocial support program to increase self-efficacy, support-seeking, and reduce loneliness among caregivers. It is hypothesized that enCompass will build self-efficacy and coping skills, serving caregivers throughout the patient's illness and complications.
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Eligibility Criteria
Inclusion Criteria:
Inclusion Criteria for Caregivers
* English-speaking.
* Ability to provide written or verbal informed consent to participate in the study;
* Willing and able to comply with study procedures based on the judgment of the investigator or protocol designee;
* Be at least 18 years o…
Inclusion Criteria:
Inclusion Criteria for Caregivers
* English-speaking.
* Ability to provide written or verbal informed consent to participate in the study;
* Willing and able to comply with study procedures based on the judgment of the investigator or protocol designee;
* Be at least 18 years of age at the time of consent; and
* Identify as an informal (unpaid) caregiver for an adult with a stage II-IV cancer AND diabetes.
Inclusion Criteria for patients
* English-speaking
* Ability to provide informed consent.
* Be at least 18 years of age at the time of consent; and
* Their identified caregiver is enrolled in the study
* Diagnoses: (must have cancer and diabetes)
* Have a cancer diagnosis for which they are being actively treated at one of the study sites
* Have a cancer diagnosis, stage II-IV solid tumor or any hematologic malignancy
* Receiving active cancer treatment s, not including hormonal therapy
* Concurrent history of diabetes with need for ongoing management
Exclusion Criteria:
Exclusion Criteria for Caregivers
* Unable to complete self-report instruments due to illiteracy, neurologic illness, inability to speak or read English, or other causes;
* Existence of another co-morbid disease other than diabetes, which in the opinion of the investigator, prohibits participation in the protocol;
* Participation in the intervention development phase of this intervention
Exclusion Criteria for patients
* Self-report instruments due to illiteracy, neurologic illness, inability to speak or read English, or other causes;
* Existence of other co-morbid disease, which in the opinion of the investigator, prohibits participation in the protocol;
* Their caregiver does not enroll in the study or withdraws consent
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