Family caregivers' lived experience of caring for hospitalised patients with cancer during the COVID‐19 lockdown: A descriptive phenomenological study

Abstract

AbstractAimsThis study aimed to capture and explore family caregivers' lived experience of caring for hospitalised patients with cancer during the lockdown.BackgroundThe unprecedented lockdown episodes due to COVID‐19 have brought significant changes in the hospital visiting policies and caregiving practices. As part of the precautionary measures for hospital visits, the bedside companion was restricted to one caregiver for patients with cancer in Shanghai hospitals.DesignThis study adopted a descriptive phenomenological approach.MethodsData were collected among 20 family caregivers recruited from the Oncology department of a tertiary hospital in Shanghai in May 2022, using purposive sampling method and followed by unstructured, open‐ended interviews. Colaizzi's seven‐step data analysis method was used to analyse the data to reveal the emergent themes and subthemes of the phenomenon.ResultsFour themes were generated on family caregivers' lived experience of caring for hospitalised patients with cancer during the lockdown, including (1) Feeling scared for the patient; (2) Living a life feeling trapped under COVID‐19 surveillance; (3) Feeling neglected and unseen; (4) Growing resilience and appreciation.ConclusionsThe lockdown exacerbated the burden of family caregivers when they cared for the hospitalised patients with cancer during the lockdown period. However, positive reframing of the lived experience facilitated their coping with the challenging situation.Relevance to Clinical PracticeFindings from this study highlighted the potential proactive roles the healthcare providers could play in improving family caregivers' health and supporting them during and beyond the COVID‐19 pandemic.Reporting MethodThe study adhered to relevant EQUATOR guidelines; the study was reported according to the COREQ checklist.Patient or Public ContributionFamily caregivers of patients with cancer were involved in data collection and member‐checking of the transcripts and interpretations of their experiences.