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An Exploratory Study of Caregiver Burden Among Family Caregivers of Patients With Cancer

An Exploratory Study of Caregiver Burden Among Family Caregivers of Cancer Patients

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03069105
Enrollment
49
Registered
2017-03-03
Start date
2017-02-23
Completion date
2020-04-28
Last updated
2020-11-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cancer, Caregivers

Brief summary

This study will look at caregiver burden and the coping behavior of caregivers of patients with cancer. Through this study, the investigators will identify the relationship between cognitive dysfunction (measured as a proxy rating by the caregiver), resilience, social support, cognitive appraisal, coping behavior, and caregiver burden, anxiety, and depression among family caregivers of patients with cancer.

Detailed description

The goal of this study is to explore caregiver burden and the coping behavior of caregivers of patients with cancer. It has been documented that non-professional caregivers and long-term care providers to patients with cancer receive little preparation, information, or support to perform their vital role. Through this study, the investigators will identify the relationship between cognitive dysfunction, resilience, social support, cognitive appraisal, coping behavior, and caregiver burden, anxiety, and depression among family caregivers of patients with cancer. The findings of this study will direct future intervention studies to reduce caregiver burden and improve outcomes for the many individuals caring for family members with cancer.

Interventions

OTHERQuestionnaire

Participants will complete paper and pencil or electronic questionnaires at the cancer center or in the privacy of their own homes.

Sponsors

Saint John's Cancer Institute
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Age ≥ 18 years * Self-identified primary caregiver of patients with cancer * Co-residence with the patient * Providing a minimum of 4 hours of direct care for at least 3 days per week * Able to speak, read, and understand English * Willing to participate in completion of surveys

Exclusion criteria

* Professional or paid caregivers

Design outcomes

Primary

MeasureTime frameDescription
Changes in Caregiver Burden Score [Caregiver Reaction Assessment (CRA)]1 yearRelation between caregiver burden subscale scores and caregiver resilience, social support, and coping

Secondary

MeasureTime frameDescription
Changes in Anxiety and Depression Score [Hospital Anxiety and Depression Scale (HADS)]1 yearRelation between caregiver anxiety and depression score and caregiver resilience, social support, and coping

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026