A Comparative Analysis of Psychological Distress and Its Impact on Quality of Life on Primary Caregivers and Their Patients Suffering from Advanced Cancer

isolation.The costs associated with medical care, medications, and potential adjustments to living arrangements can create a financial burden. 6All these factors compromise the caregivers' QoL.Thus, identifying and resolving caregivers' psychological distress and enhancing their QoL is crucial to creating efficient support and intervention strategies.By understanding and attending to the unique needs and despite the difficulties caregivers encounter, it is feasible to raise their general QoL and improve their well-being. IntroductIonPatients with advanced cancer suffer from various debilitating symptoms, causing functional impairment during the disease course and mainly during the last stages of their life.Thus, they need support from others to manage various self-care activities. 1 Caregivers who are providing uncompensated care to the cancer patients are mainly their family members.They not only help patients in their routine daily activities but also provide them with adequate emotional support. 2 The emotional toll of witnessing a loved one's suffering, managing complex treatment plans, and navigating the uncertainties of the disease can lead to high level of stress and emotional strain.Over time, this can result in burnout and a decline in the caregivers' mental well-being. 3uality of life (QoL) refers to various aspects of well-being including physical health, emotional stability, social engagement, and overall life satisfaction.Caregivers frequently report reduced QoL due to the demanding nature of caregiving responsibilities. 4he constant need for vigilance, administering medications, and attending to the patient's various needs can result in sleep deprivation and chronic fatigue.The relentless demands of caregiving may also limit personal time and opportunities for self-care, contributing to a sense of isolation and neglect of one's own needs. 5The progressive decline of the patient's health may limit the caregiver's ability to engage in social activities, leading to social 1,