2021
DOI: 10.3390/ijerph18062964
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Caring for Patients with Psychosis: Mental Health Professionals’ Views on Informal Caregivers’ Needs

Abstract: The aim of this study was to explore the views of mental health professionals regarding the needs of the informal caregivers of patients with chronic psychotic syndrome. A qualitative research design was used. The sample consisted of 12 mental health professionals selected by a purposive sampling strategy. Data were collected through semistructured, face to face interviews. Framework analysis was used to analyze qualitative data and establish main themes and subthemes. Three main themes emerged namely, (i) imp… Show more

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Cited by 7 publications
(5 citation statements)
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References 69 publications
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“…The caregivers of psychiatric patients are a vulnerable group ( 68 ) that is sometimes neglected while the condition of the patients can affect them. Findings indicate that caregivers are more likely to have psychological problems in comparison with the general population ( 69 , 70 ).…”
Section: Discussionmentioning
confidence: 99%
“…The caregivers of psychiatric patients are a vulnerable group ( 68 ) that is sometimes neglected while the condition of the patients can affect them. Findings indicate that caregivers are more likely to have psychological problems in comparison with the general population ( 69 , 70 ).…”
Section: Discussionmentioning
confidence: 99%
“…Having a patient can greatly impact the social relationships of family caregivers. Distance from family members, friends and acquaintances, 15 27 32 33 educational and occupational problems among family members, 20 34 disruption of leisure and recreation, 21 imbalance between one’s job and patient care, social stigma, 16 17 31 35 negative attitudes, discrimination and prejudice, 15 isolation of both caregivers and patients 23 24 36 and conflict over disease disclosure 37 are among the social challenges for these caregivers. As such, there is a need to improve communication with relatives, community members and the treatment team.…”
Section: Psychosocial Challenges Of Caregiversmentioning
confidence: 99%
“…Family caregivers of patients with CMD suffer from many emotional and social problems from the time of encountering the illness. Psychological and emotional burdens of care, 21 33 37 feelings of helplessness, 1 24 36 feelings of shame and embarrassment, 21 24 36 38 anger, fear, depression and anxiety, 1 21 23 24 39 boring and monotonous lives, 21 32 lack of peace and security, 21 concern about the future of the caregivers themselves, 15 21 feelings of distress and sadness, 18 23 24 31 33 frustration caused by the chronic course of the disease, 7 a sense of guilt, self-blame or blame of the patient, 16 23 24 33 36 concern about the patient’s future, 15 23 26 31 decreased quality of life, 36 feelings of losing one’s identity, 40 concern about patients’ tendency to have violent behaviors, 21 31 hiding the disease, 36 feelings of inadequacy and victimization, emotional burnout, 40 low self-esteem, 36 care-caused fatigue and stress, 33 involvement in different roles and change of roles 1 40 are among the psychological challenges that families face.…”
Section: Psychosocial Challenges Of Caregiversmentioning
confidence: 99%
“…As such, Chinese people are likely to keep their ill family member a secret in order to avoid face loss. The above psychological process is likely to create distress and subjective burden, symptoms of depression and anxiety [ 14 ], social isolation [ 15 ], and reduced community engagement [ 16 ]. Consequently, caregivers may become less motivated to seek help from mental health services, leaving their voices ignored and not heard.…”
Section: Introductionmentioning
confidence: 99%