Timely short-term specialised palliative care service intervention for frail older people and their family carers in primary care: study protocol for a pilot randomised controlled trial

被引:4
|
作者
de Nooijer, Kim [1 ]
Pivodic, Lara [1 ]
Van den Noortgate, Nele [1 ,2 ]
Pype, Peter [1 ,3 ]
Van den Block, Lieve [1 ,4 ]
机构
[1] Vrije Univ Brussel, Dept Family Med & Chron Care, End Life Care Res Grp, Brussels, Belgium
[2] Univ Hosp Ghent, Dept Geriatr Med, Ghent, Belgium
[3] Univ Ghent, Dept Publ Hlth & Primary Care, Ghent, Belgium
[4] Vrije Univ Brussel, Dept Clin Sci, Brussels, Belgium
来源
BMJ OPEN | 2021年 / 11卷 / 01期
基金
比利时弗兰德研究基金会;
关键词
palliative care; primary care; adult palliative care; INITIAL VALIDATION; SUPPORTIVE CARE; CANCER-PATIENTS; OUTCOME MEASURE; QUESTIONNAIRE; PREVALENCE; INSTRUMENT; SECURITY; DISEASE; ADULTS;
D O I
10.1136/bmjopen-2020-043663
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction There is limited evidence regarding the effectiveness of timely integration of short-term specialised palliative care services for older people in primary care. Using a Theory of Change approach, we developed such an intervention, the Frailty+ intervention. We present the protocol of a pilot randomised controlled trial (RCT) with a process evaluation that aims to assess the feasibility and preliminary effectiveness of the Frailty+ intervention. Methods and analysis We will conduct a pilot RCT in Flanders, Belgium. Frail older people who are discharged to home from hospital will be identified and recruited. Seventy-six will be randomly assigned either to the control group (standard care) or the intervention group (Frailty+ intervention alongside standard care). Data will be collected from patients and family carers. At the core of the Frailty+ intervention is the provision of timely short-term specialised palliative care facilitated by a nurse from the specialised palliative home care service over a period of 8 weeks. We will assess feasibility in terms of recruitment, randomisation, acceptability of the intervention, retention in the programme and data completion. The primary outcome for assessing preliminary effectiveness is a mean score across five key symptoms that are amenable to change (ie, breathlessness, pain, anxiety, constipation, fatigue), measured at baseline and 8 weeks post-baseline. The process evaluation will be conducted in the intervention group only, with measurements at 8-11 weeks post-baseline to evaluate implementation, mechanisms of change and contextual factors. Ethics and dissemination The study has been approved by the ethics committee of University Hospital Ghent. Results will be used to inform the design of a full-scale RCT and will be published in a peer-reviewed, open access journal.
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页数:11
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