{"title":"Enhancing Bereavement Experiences for Family Caregivers of Cancer Patients: A Pilot Intervention Study.","authors":"Yutaka Hatano, Isseki Maeda, Kaoru Nishijima, China Kamei, Keisuke Ariyoshi, Shunsuke Oyamada","doi":"10.1089/jpm.2024.0090","DOIUrl":null,"url":null,"abstract":"<p><p><b><i>Background:</i></b> Although hospice care is associated with better bereavement outcomes, the duration of hospice care at the end of life remains very short. <b><i>Objective:</i></b> The aim was to assess the feasibility of the study methods and to measure the impact of a novel brief intervention on bereaved family caregivers' satisfaction and their psychological distress and psychological burden in nurses. <b><i>Method:</i></b> Family caregivers of patients with cancer in an inpatient hospice were recruited. Participants provided information about the patient's personality and photographs of the patient before the illness. Researchers used this information to create a self-introduction sheet and placed it in the patient's room. Family caregivers were asked to complete pre- and post-intervention measures of satisfaction, depression, and grief. Nurse satisfaction was also assessed. <b><i>Results:</i></b> Twenty-one participants received the intervention. Sixteen participants completed the postbereavement assessments. At three months postbereavement, 100% of bereaved caregivers \"absolutely agreed\" or \"agreed\" with the subdomain \"I was satisfied with the sheet.\" More than 76% of them \"absolutely agreed\" or \"agreed\" with other subdomains. The average score of the Patient Health Questionnaire-9 showed a significant decrease between pre- and post-intervention (7.2 vs. 4.4, <i>p</i> = 0.014). More than 80% of the nurses rated \"absolutely agree\" or \"agree\" with all subdomains of the satisfaction scale. <b><i>Conclusions:</i></b> The results suggest that our approach can be acceptable. Further research is needed to facilitate implementation and to compare the impact on caregiver psychological distress with a control group.</p>","PeriodicalId":16656,"journal":{"name":"Journal of palliative medicine","volume":" ","pages":""},"PeriodicalIF":2.2000,"publicationDate":"2025-03-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of palliative medicine","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1089/jpm.2024.0090","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"HEALTH CARE SCIENCES & SERVICES","Score":null,"Total":0}
引用次数: 0
Abstract
Background: Although hospice care is associated with better bereavement outcomes, the duration of hospice care at the end of life remains very short. Objective: The aim was to assess the feasibility of the study methods and to measure the impact of a novel brief intervention on bereaved family caregivers' satisfaction and their psychological distress and psychological burden in nurses. Method: Family caregivers of patients with cancer in an inpatient hospice were recruited. Participants provided information about the patient's personality and photographs of the patient before the illness. Researchers used this information to create a self-introduction sheet and placed it in the patient's room. Family caregivers were asked to complete pre- and post-intervention measures of satisfaction, depression, and grief. Nurse satisfaction was also assessed. Results: Twenty-one participants received the intervention. Sixteen participants completed the postbereavement assessments. At three months postbereavement, 100% of bereaved caregivers "absolutely agreed" or "agreed" with the subdomain "I was satisfied with the sheet." More than 76% of them "absolutely agreed" or "agreed" with other subdomains. The average score of the Patient Health Questionnaire-9 showed a significant decrease between pre- and post-intervention (7.2 vs. 4.4, p = 0.014). More than 80% of the nurses rated "absolutely agree" or "agree" with all subdomains of the satisfaction scale. Conclusions: The results suggest that our approach can be acceptable. Further research is needed to facilitate implementation and to compare the impact on caregiver psychological distress with a control group.
期刊介绍:
Journal of Palliative Medicine is the premier peer-reviewed journal covering medical, psychosocial, policy, and legal issues in end-of-life care and relief of suffering for patients with intractable pain. The Journal presents essential information for professionals in hospice/palliative medicine, focusing on improving quality of life for patients and their families, and the latest developments in drug and non-drug treatments.
The companion biweekly eNewsletter, Briefings in Palliative Medicine, delivers the latest breaking news and information to keep clinicians and health care providers continuously updated.