Caregiver-Guided Pain Management Training in Palliative Care

姑息治疗中护理人员指导的疼痛管理培训

• 批准号: 8932804
• 负责人: Francis J. Keefe
• 金额: $ 53.3万
• 依托单位: DUKE UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2014
• 资助国家: 美国
• 起止时间: 2014-09-26 至 2018-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8932804
• 关键词: Aftercare; Back; Behavioral; Bereavement; Cancer Patient; Caregivers; Caring; Cessation of life; Coping Skills; Distress; Educational Intervention; Educational Materials; Educational process of instructing; Ensure; Family; Family Caregiver; Family member; Goals; Guided imagery; Health; Healthcare; Hour; Imagery; Intervention; Lead; Malignant Neoplasms; Methods; Outcome; Pain; Pain management; Pain quality; Palliative Care; Patients; Pilot Projects; Protocols documentation; Quality of life; Randomized; Relaxation; Reporting; Research; Research Design; Research Priority; Resources; Sample Size; Sampling; Self Efficacy; Severities; Site; Techniques; Testing; Training; Training Programs; Videoconferences; Videoconferencing; cancer pain; caregiving; coping; efficacy testing; end of life; experience; follow-up; hospice environment; improved; loved ones; meetings; member; novel; psychologic; psychological distress; psychosocial; satisfaction; symptom management; therapy design; treatment as usual; trend

DESCRIPTION (provided by applicant): Pain at the end of life is a major concern of cancer patients and their family caregivers. The focus of pain management efforts for cancer pain traditionally has been on the patient. Studies of family members, however, have documented that the psychosocial impact of end of life care is profound, particularly when the patient is experiencing pain. For family caregivers, this impact endures--often resulting in increased psychological distress and poorer health long after their loved one dies. The ultimate goal of this research is to develop more effective ways to help patients and their family caregivers cope with cancer pain and thereby reduce the psychological distress associated with pain for the patient and the short-term and enduring negative effects of the caregiving experience for their family members. We recently completed a small pilot study to test a novel Caregiver-Guided Pain Management Training protocol that trained hospice-eligible patients with cancer pain and their family caregivers in behavioral pain coping skills (e.g., relaxation, guided imagery, activity pacing) and taught them how to apply coping skills to manage negative pain-related sequelae and enhance their quality of life. Results indicated that the intervention led to significant improvements in caregiver self-efficacy for helping patients manage pain, and trends for improvements in caregiver strain and patient pain. The proposed study builds on and extends these findings by (a) utilizing the resources and support of the PCRC to access a larger and more diverse sample of patients and their informal caregivers; (b) delivering the intervention via videoconference to increase access and potential for dissemination; and (c) assessing the impact of the intervention on caregiver adjustment after the patient's death. To our knowledge, this will be the first RCT to rigorously examine whether a pain coping skills intervention designed to improve the caregiver's ability to help the patient manage pain at end of life can lead to caregiver benefits during the bereavement period. In this multi-site study, 236 dyads (patients and their family caregivers) will be randomized to either the Caregiver-Guided Pain Management Training protocol or to an Enhanced Treatment-as-Usual control condition. Dyads in the Caregiver-Guided Pain Management condition will receive three one-hour sessions conducted via videoconference. Dyads in the Enhanced Treatment-as-Usual condition will receive educational material about cancer pain and its management but will not receive any study-related treatment sessions. Assessments will be conducted with patients and caregivers before and after treatment, and with caregivers 3 months and 6 months following the patient's death. The primary hypothesis to be tested is that caregivers who receive the intervention will report significantly higher levels of self-efficacy for helping the patient manage pain than caregivers in the control condition. Secondary aims will focus on (a) improvements in short-term caregiver adjustment as well as caregiver adjustment following the patient's death, and (b) patient pain severity, self-efficacy for pain management, and psychological distress.

描述（由申请人提供）：临终时的疼痛是癌症患者及其家属关心的主要问题。传统上，癌症疼痛管理工作的重点一直放在患者身上。然而，对家庭成员的研究表明，临终关怀的心理社会影响是深远的，特别是当病人正在经历痛苦时。对于家庭照顾者来说，这种影响会持续下去，往往会在亲人去世后很长一段时间内导致心理困扰增加，健康状况恶化。这是最终的目标