“The Ability to Go Out into the World Is the Most Important Thing”—A Qualitative Study of Important Exercise Outcomes for People with Lung Cancer

Author:

Bowman Amy12ORCID,Denehy Linda13ORCID,McDonald Cassie E.14ORCID,Edbrooke Lara13ORCID

Affiliation:

1. Department of Physiotherapy, The University of Melbourne, Melbourne, VIC 3053, Australia

2. Department of Physiotherapy, Peter Mac Callum Cancer Centre, Melbourne, VIC 3000, Australia

3. Department of Health Services Research, Peter Mac Callum Cancer Centre, Melbourne, VIC 3000, Australia

4. Allied Health, Alfred Health, Melbourne, VIC 3004, Australia

Abstract

Whilst existing quantitative research identifies outcomes believed to be important by researchers and clinicians, it may neglect outcomes that are meaningful to patients. This study aimed to explore the outcomes of exercise that are important to people with lung cancer and their carers. Data collection involved a qualitative methodology including semi-structured interviews and focus groups. Question guide development was informed by the International Classification of Functioning (ICF) framework. Data were analyzed by two researchers with NVivo (v12) software using a conventional content analysis process, followed by directed content analysis to map outcomes to the ICF. Conduct and reporting adhered to COREQ guidelines. Fifteen participants provided data. Most participants had received their diagnoses 24 months prior to study involvement (n = 9), and one-third had completed treatment (n = 5). Important outcomes were reported by participants across all domains of the ICF: activity and participation (n = 24), body function (n = 19), body structure (n = 5), environmental factors (n = 5), and personal factors (n = 1). Additional code categories pertained to the impacts of non-cancer factors such as age, frailty, and comorbidities; identifying barriers to exercise; and individualizing outcome measures. Clinicians and researchers should consider selecting outcomes from all relevant domains of the ICF, with a focus on the activity and participation domain, in addition to non-cancer factors such as ageing, frailty, and co-morbidities. Feedback should be provided to patients following outcome measures collection and reassessment.

Funder

University of Melbourne

Publisher

MDPI AG

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