Expanding the Support of Family Caregivers of Diverse Patients With Cancer and Diabetes

ConditionsCancerDiabetes
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-99
SponsorUNC Lineberger Comprehensive Cancer Center

About this trial

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.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

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

Disqualifiers

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

Self-report instruments due to illiteracy, neurologic illness, inability to speak or read English, or other causes;

Trial design

Design model

Crossover

Treatments tested in this trial

  • Survey

    Behavioral

    Participants will receive up to eight coaching sessions with a caregiver coach and resource materials and access to an online tool designed to help caregivers find resources.

  • the resource booklet from the American Cancer Society

    Other intervention

    The caregiver will receive the resource booklet from the American Cancer Society.

Treatment groups

162 Participants
are divided into 2 treatment groups
Group A: caregiversExperimental treatment 1 intervention
Group B: caregiverActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Acceptability of the Intervention Measure (AIM)

The AIM is a 4-item, 5-point Likert scale that measures intervention acceptability. The scale measures each statement from 1, "Completely disagree," to 5, "Completely agree." Scale items are averaged to produce a mean score. The AIM takes approximately 2 minutes to complete by caregivers.

Time frame
8 weeks

Secondary outcomes

1

Coping Self-Efficacy Scale (CSES)

The Coping Self-Efficacy Scale is a 26-item, 10-point ordinal scale that measures caregiver coping and self-efficacy ability. Subjects are asked to self-score their confidence in each prompt on a scale from 0 (Cannot do at all) to 10 (Certain I can do). An overall CSES score is created by summing the item ratings (total score range, 0 - 260), with higher scores indicating greater perceived coping self-efficacy. Subjects must answer at least 80% of the scale items. For subjects missing an item or items, an individual's score for the missing item(s) is estimated by adding in their mean for the items that they answered for each item that they skipped, resulting in a "corrected sum." This measure will take approximately 7 - 10 minutes to complete by caregivers.

Time frame
Baseline, 8 weeks, 6 months
2

Zarit Burden Assessment - Revised

The Zarit Burden Assessment - Revised is a commonly used, 12-item self-report scale measuring caregiver burden. The Zarit Burden Assessment-Revised has excellent internal consistency (Cronbach's alpha typically ranges from 0.83 to 0.89) and test-retest reliability (typically around 0.71). The measure typically takes 5-10 minutes to completeby caregivers.

Time frame
Baseline, 8 weeks, 6 months
3

Duke-UNC Functional Support Questionnaire (FSSQ)

The Duke-UNC FSSQ is an 8-item, multidimensional scale measuring perceived social support. Response items are scored from 5 ("as much as I would like") to 1 ("much less than I would like"). The scores from all eight questions are summed for a total score range of 8 to 40, with higher scores indicating higher perceived support. The Duke-UNC FSSQ has demonstrated high reliability and convergent validity. This measure will take approximately 3-5 minutes to complete by caregivers.

Time frame
Baseline, 8 weeks, 6 months
4

Hospital Anxiety and Depression Scale (HADS) - Caregivers

The HADS is a 14-item, 4-point, self-report ordinal scale that measures depression and anxiety symptom severity. It is a well-validated and commonly used measure in both ill and healthy populations. It has two sub-scales, each with a total score range of 0 - 21, with higher scores suggesting more symptoms. Current research supports a threshold of 8 or higher as indicative of clinically significant depression or anxiety symptoms. The HADS takes approximately 3-5 minutes to complete by caregivers.

Time frame
Baseline, 8 weeks, 6 months

Other outcomes

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