Author:
van der Wel Maaike,van der Smissen Doris,Dierickx Sigrid,Cohen Joachim,Hudson Peter,De Vleminck Aline,Tutt Lydia,Scott David,Di Leo Silvia,Arnfeldt Caroline Moeller,Jordan Catherine,Northouse Laurel,Rietjens Judith,van der Heide Agnes,Witkamp Erica
Abstract
Abstract
Purpose
Having advanced cancer presents many challenges for patients and family caregivers. The FOCUS program is a psychoeducational nurse-led intervention, developed in the USA, to support dyads of patients with cancer and their family caregivers to live with the illness. The program includes a conversation manual and information resources for dyads. We aimed to develop a version of the program for dyads facing advanced cancer in six European countries.
Method
The Participatory and Iterative Process Framework for Language Adaptation (PIPFLA) was used to guide the translation of the program to the local contexts of Belgium, Denmark, Ireland, Italy, the Netherlands, and the UK. In several rounds, potential program users (e.g., nurses, clinicians, patients, family caregivers) and researchers from all six countries reviewed program materials and advised on adaptations.
Results
The PIPFLA process resulted in one European version of the program in different languages (FOCUS +). The FOCUS + conversation manual is uniform across all countries. The main adaptations included additional attention to both family caregiver and patient needs; more emphasis on self-management, advance care planning, and shared responsibilities; discussing the dyad’s outlook rather than optimism; addressing the role of nurses as educational rather than therapeutic; and more suggestions to refer dyads to health care professionals for specific care needs. The information resources for dyads were adapted to fit with local contexts.
Conclusion
The PIPFLA methodology is an efficient and effective framework to thoroughly translate and culturally adapt a complex USA-based program for use in six European countries in collaboration with end users.
Funder
European Union's Horizon 2020 research and innovation program
HSC R&D Division, Public Health Agengy Northern Ireland
Publisher
Springer Science and Business Media LLC
Reference30 articles.
1. Clark MM, Rummans TA, Sloan JA, Jensen A, Atherton PJ, Frost MH, Richardson JW, Bostwick JM, Johnson ME, Hanson JM (2006) Quality of life of caregivers of patients with advanced-stage cancer. Am J Hosp Palliat Med 23:185–191. https://doi.org/10.1177/1049909106289074
2. Payne S (2010) White paper on improving support for family carers in palliative care: Part 1: recommendations from the European association for palliative care (EAPC) task force on family carers. European Journal of Palliative Care 17:238–245
3. Stajduhar KI, Funk L, Toye C, Grande GE, Aoun S, Todd CJ (2010) Part 1: Home-based family caregiving at the end of life: a comprehensive review of published quantitative research (1998–2008). Palliat Med 24:573–593. https://doi.org/10.1177/0269216310371412
4. Chang Y, Kwon YC, Lee WJ, Do YR, Lee KS, Kim HT, Park SR, Hong YS, Chung I, Yun YH (2013) Burdens, needs and satisfaction of terminal cancer patients and their caregivers. Asian Pac J Cancer Prev 14:209–215. https://doi.org/10.7314/apjcp.2013.14.1.209
5. Soylu C, Ozaslan E, Karaca H, Ozkan M (2016) Psychological distress and loneliness in caregiver of advanced oncological inpatients. J Health Psychol 21:1896–1906. https://doi.org/10.1177/1359105314567770
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