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A Study of Family Caregivers' Needs, Burden of Care and Quality of Life Over the Course of a Cancer Illness

A Study of Family Caregivers' Needs, Burden of Care and Quality of Life Over the Course of a Cancer Illness

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03081312
Acronym
FCG-NBC
Enrollment
510
Registered
2017-03-16
Start date
2017-03-01
Completion date
2019-02-28
Last updated
2018-04-10

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

Conditions

Cancer, Family Caregivers, Health Related Quality of Life

Keywords

Family Cancer Caregivers,, Needs, Burden of Care, Quality of Life

Brief summary

This research will determine (a) the unmet needs of family caregivers of adult cancer patients and (b) determine the impact on stress, care burden and quality of life. A cross-sectional questionnaire methodology will be used to answer the research questions. 510 family caregivers at different stages of patients' cancer journey will be recruited. The study duration is expected to take two years. Research findings will address the knowledge gap of caregivers' needs and stress, burden and quality of life and support plans to help caregivers.

Detailed description

The literature suggests that caregivers have unique psychological, emotional and lifestyle needs but there is a paucity of such information of caregivers in Singapore. As this study is exploratory, no a priori hylothesis has been made. The theoretical framework guiding this research is Fulfillment Theory in which the existence and perception of needs and need fulfillment are hypothesized to be antecedents to the experience of satisfaction about care. A cross-sectional questionnaire methodology will be used to answer the research questions. Caregivers in this study are defined as: a family member who lends physical, emotional or other support to someone at any time during the cancer journey. A power calculation was not done, instead the sample size of 510 was based on what may be practically achievable and feasible for the duration of the short-term quantitative study. Descriptive statistics will be used to characterize the distribution of socio-demographic characteristics and caregiver-related information. Regression analysis will be used to evaluate difference in overall and domain specific needs across selected characteristics. Problems identified by caregivers will be dichotomized as present or absent and chi-square tests will be used to evaluate associations with selected characteristics.

Interventions

None listed

Sponsors

National University of Singapore
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
21 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

an adult providing care for a familyt member with cancer aged between 21 and 90 years and willing to participate in the study

Exclusion criteria

caregiving adults who are not family members and not willing to particfipate in the study

Design outcomes

Primary

MeasureTime frameDescription
Needs of family cancer caregiversOne yearNeeds Assessment of Family Caregivers-Cancer (NAFC-C) questionnaire

Countries

Singapore

Contacts

Primary ContactRathi Mahendran, MMed(Psych)
rathi_mahendran@nuhs.edu.sg67725555

Outcome results

None listed

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