Self-Management Components as Experienced by People with Parkinson’s Disease and Their Carers: A Systematic Review and Synthesis of the Qualitative Literature

<table class="table-group" id="tab1"><tr><td><table class="table"><tr><td class="thead-hr" colspan="2"><hr/></td></tr><tr class="thead"><td class="align_left">Inclusion criteria</td><td class="align_center">Exclusion criteria</td></tr><tr><td class="thead-hr" colspan="2"><hr/></td></tr><tr><td class="align_left">People with idiopathic Parkinson’s disease living in the community, or carers of people with Parkinson’s disease</td><td class="align_center">Atypical Parkinsonism, life expectancy &lt;6 months, other illnesses, healthy individuals, hospital based (in-patient) populations, or living in a care home</td></tr><tr><td class="align_left">Qualitative research, reported in full text in English</td><td class="align_center">Quantitative research design, survey, closed questionnaire, reviews, protocols, editorials, commentary, conference abstracts, non-English full text papers</td></tr><tr><td class="align_left">Experiences related to self-management such as but not limited to health-related quality-of-life, psychological and physical health outcome, and generalized self-efficacy</td><td class="align_center">Not related to self-management, e.g., diagnosis, service use, end of life care</td></tr><tr class="table-tr"><td colspan="2"><hr class="tbody-hr"/></td></tr></table></td></tr></table>

<div>Inclusion and exclusion criteria.</div>

Parkinson’s Disease

tab1

Table 1

Table 1: Self-Management Components as Experienced by People with Parkinson’s Disease and Their Carers: A Systematic Review and Synthesis of the Qualitative Literature 

Table 1 | Self-Management Components as Experienced by People with Parkinson’s Disease and Their Carers: A Systematic Review and Synthesis of the Qualitative Literature 