Tofthagen Cindy, Sheffield Kathy, Pachman Deirdre R, Mandrekar Jay, Szalacha Laura A, Chesak Sherry S, Rhudy Lori M, Kilpatrick Molly, Buck Harleah
Division of Nursing Research, Mayo Clinic, Jacksonville, FL, USA.
Division of Community Internal Medicine, Geriatrics, and Palliative Care, Mayo Clinic, Rochester, MN, USA.
Am J Hosp Palliat Care. 2024 Sep 5:10499091241282417. doi: 10.1177/10499091241282417.
The objective of this manuscript is to present the protocol of a study aiming to test the effects of Accelerated Resolution Therapy® (ART) on pre-loss grief and prolonged grief among older adult family caregivers. This study also aims to better understand predictors of response to ART®, and cognitive processes that occur among grieving individuals following ART®.
The study is a double-blinded, randomized clinical trial.
This study takes place at both inpatient and outpatient palliative care and hospice programs at two Mayo Clinic sites.
Participants include older adult ( 60 years) immediate family members who are primary caregivers of someone with an advanced illness and life expectancy of less than 12 months.
Participants are randomized to either the ART® intervention group or the attention control group. In the ART® intervention, caregivers engage in imaginal exposure, lateral eye movements, and imagery rescripting via 4 sessions lasting 1-1.5 hours each. The attention control group receives a standard social work intervention, including education, resources, and active listening, which is matched for time and attention. Both interventions will longitudinally follow caregivers from active caregiving into bereavement.
The primary outcomes of pre-loss grief and prolonged grief will be measured with the Pre-Loss Grief 12 item (PG-12-R) before the care recipient's death, and with the Prolonged Grief-13 (PG-13-R) afterwards.
本手稿的目的是介绍一项研究方案,该研究旨在测试加速解决疗法(ART)对老年家庭照顾者丧失前悲伤和持续性悲伤的影响。本研究还旨在更好地了解对ART反应的预测因素,以及悲伤个体在接受ART后发生的认知过程。
该研究为双盲随机临床试验。
本研究在梅奥诊所两个地点的住院和门诊姑息治疗及临终关怀项目中进行。
参与者包括60岁及以上的成年直系家庭成员,他们是患有晚期疾病且预期寿命少于12个月患者的主要照顾者。
参与者被随机分为ART干预组或注意力控制组。在ART干预中,照顾者通过4次每次持续1 - 1.5小时的疗程进行想象暴露、横向眼球运动和意象改写。注意力控制组接受标准的社会工作干预,包括教育、资源和积极倾听,干预时间和关注度与之匹配。两种干预措施都将对照顾者从积极照顾阶段到丧亲阶段进行纵向跟踪。
在受照顾者死亡前,用12项丧失前悲伤量表(PG - 12 - R)测量丧失前悲伤和持续性悲伤的主要结果,之后用13项持续性悲伤量表(PG - 13 - R)进行测量。