Cancer
Conditions
Keywords
social support, rural, caregivers, coaching
Brief summary
This study explores the feasibility, acceptability, and preliminary efficacy of a social support intervention in cancer caregivers who live in rural communities. Cancer caregivers need support, especially when they live at a distance from healthcare centers. enCompass Carolina is a social support intervention, that supports caregivers by helping them find and use new sources of support. The purpose of this study is to test and receive feedback about the program.
Interventions
BEHAVIORALEco-mapping tool
The web application allows caregivers to visually identify and organize their existing social network (family, friends, community of worship, and others) to assist with their support needs, tailored to their context. For each of the six support social support domains (in-home, informational, communication, financial, emotional and spiritual, transportation (e.g., emotional, informational, practical), the enCompass web application prompts the individual to identify members of their network. After completing each domain, caregivers are presented with a visual social support
BEHAVIORALCaregiver-coach study visits
Caregivers engage in up to 8 manualized, telephone/videoconference visits with a trained caregiver coach. The caregiver coach uses the study manual and interview guide to provide support for caregiver support-seeking and problem-solving.
Sponsors
The Duke Endowment
UNC Lineberger Comprehensive Cancer Center
Study design
Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
Inclusion criteria for caregivers In order to participate in this study a subject must meet all of the eligibility criteria outlined below. 1. English-speaking. 2. Ability to provide written or electronic informed consent to participate in the study. 3. Subject is willing and able to comply with study procedures based on the judgment of the investigator or protocol designee. 4. Age ≥ 18 years at the time of consent. Identify as an informal (unpaid) caregiver for a rural-dwelling adult with a stage II-IV solid tumor or any hematologic malignancy in active treatment (see eligibility criteria for patients). Inclusion criteria for subjects with cancer In order to participate in this study a subject must meet all of the eligibility criteria outlined below. 1. Their identified caregiver is enrolled in the study 2. English-speaking. 3. Ability to provide written or electronic informed consent to participate in the study. 4. Subjects are willing and able to comply with study procedures based on the judgment of the investigator or protocol designee. 5. Age ≥ 18 years at the time of consent. Have a diagnosis of stage II-IV solid tumor or any hematologic malignancy receiving active treatment s, not including hormonal therapy 7\. Live in a rural area according to the USDA's Rural/Urban Commuting Area (RUCA) score of \>4.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Study feasibility - caregiver enrollment | 8 weeks | Study feasibility will be measured by caregiver enrollment rates, defined as the proportion of eligible caregivers approached about the study who consent to participate. |
| Study feasibility - Caregiver intervention engagement | 8 weeks | Study feasibility will be measured by caregiver intervention engagement, defined as the proportion of enrolled caregiver subjects who receive at least one intervention visit. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Intervention acceptability-qualitative | 4 weeks, 8 weeks | Intervention acceptability will be measured using the Acceptability of the Intervention Measure (AIM) survey scores. AIM is a survey questionnaire that includes 4 questions. Response Scale: 1 = Completely disagree, 2 = Disagree, 3 = Neither agree nor disagree, 4 = Agree, 5 = Completely agree. Scoring Instructions: Scales can be created for each measure by averaging responses. Scale values range from 1 to 5. No items need to be reverse-coded. |
| Intervention acceptability-quantitative | 4 weeks, 8 weeks | Intervention acceptability will be evaluated using thematic analysis of post-intervention semi-structured interviews. |
| Caregiver self-efficacy | Baseline, 4 weeks, 8 weeks | Caregiver self-efficacy will be measured using the Coping Self-Efficacy Scale (CSES). The CSES is a 26-item measure of one's confidence in performing coping behaviour when facing life challenges. It measures the use of problem-focused coping, receiving of social support and stopping unpleasant emotions and thoughts. Scores range from not at all confident=0 to very confident=100. A score of 0 means 'extremely low self efficacy' and a score of 100 means 'extremely high self efficacy'. |
Countries
United States
Outcome results
None listed