Perceived benefits from peer‐support among family caregivers of people with amyotrophic lateral sclerosis and cognitive impairments in a palliative rehabilitation blended online learning programme

Author:

Olesen Lene Klem12ORCID,la Cour Karen3,Thorne Sally4,With Heidi1,Handberg Charlotte12ORCID

Affiliation:

1. The National Rehabilitation Center for Neuromuscular Diseases, (RCFM) Aarhus Denmark

2. Department of Public Health, Faculty of Health University of Aarhus Aarhus Denmark

3. Occupational Science, the Research Unit of User Perspectives and Community‐based Interventions University of Southern Denmark Odense Denmark

4. School of Nursing University of British Columbia Vancouver British Columbia Canada

Abstract

AbstractRationaleFamily caregivers of persons with amyotrophic lateral sclerosis and cognitive and/or behavioural impairments (PALS/CIs) experience various challenges and needs, including emotional and practical support from peers. Various forms of peer‐support have shown different strengths and weaknesses; however, little is known about how family caregivers of PALS/CIs interact with and perceive virtual face‐to‐face peer‐support.Aims and ObjectivesThe aim of this study was to understand how caregivers of PALS/CIs interact with and perceive virtual face‐to‐face peer‐support in a palliative rehabilitation programme designed to promote targeted palliative rehabilitation initiatives for caregivers of PALS/CIs.MethodA qualitative design using participant observations of 17 recorded virtual group‐facilitated meetings from two rounds of a 4‐month intervention was performed. The Medical Research Council framework, the inductive interpretive description methodology and the theoretical framework of Sense of Coherence guided the study. Nineteen participants, divided into four groups, were included.ResultsThree themes emerged: ‘Relating my situation to others, ‘Making room for forbidden thoughts and ‘Longing for normalcy. The themes reflected the various ways participants interacted in online group meetings and how the interactions evolved around practical, emotional and forbidden thoughts. Sharing personal and sorrowful concerns and frustrations engendered feelings of trust and a sense of belonging, which empowered the participants to address their genuine wish and longing for normalcy with all the trivialities of which ALS/CIs had robbed them.ConclusionVirtual face‐to‐face peer‐support can enable caregivers of PALS/CIs to share experiences of everyday life challenges that cannot always be shared elsewhere. Being able to relate to and learn from other's experiences alleviated feelings of loneliness, frustration, and concerns and thereby enhanced comprehensibility, manageability and meaningfulness. Online palliative rehabilitation interventions should provide an opportunity for caregivers to meet regularly in interactive group meetings. Familiarization takes time online and is necessary to improve their sense of feeling safe to share their deepest thoughts. Such group interventions, facilitated by trained healthcare professionals, offer a means to support dynamic group interactions and discussion of sensitive topics.

Publisher

Wiley

Subject

Public Health, Environmental and Occupational Health,Health Policy

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