Please use this identifier to cite or link to this item:
http://hdl.handle.net/1893/32018
Appears in Collections: | Faculty of Health Sciences and Sport Journal Articles |
Peer Review Status: | Refereed |
Title: | Feasibility study to assess the effect of a brief mindfulness intervention for patients with chronic obstructive pulmonary disease: A randomized controlled trial |
Author(s): | Perkins-Porras, Linda Riaz, Muhammad Okekunle, Adeoba Zhelezna, Svitlana Chakravorty, Indranil Ussher, Michael |
Keywords: | aged anxiety chronic obstructive lung disease complication controlled study depression dyspnea feasibility study female happiness human male mental stress middle aged mindfulness procedures psychological rating scale psychology randomized controlled trial very elderly, Aged Aged, 80 and over Anxiety Depression Dyspnea Feasibility Studies Female Happiness Humans Male Middle Aged Mindfulness Psychiatric Status Rating Scales Pulmonary Disease, Chronic Obstructive Stress, Psychological |
Issue Date: | 1-Nov-2018 |
Date Deposited: | 27-Nov-2020 |
Citation: | Perkins-Porras L, Riaz M, Okekunle A, Zhelezna S, Chakravorty I & Ussher M (2018) Feasibility study to assess the effect of a brief mindfulness intervention for patients with chronic obstructive pulmonary disease: A randomized controlled trial. Chronic Respiratory Disease, 15 (4), pp. 400-410. https://doi.org/10.1177/1479972318766140 |
Abstract: | Psychological distress is common among patients with chronic obstructive pulmonary disease (COPD). This study aimed to assess whether a 10-minute mindfulness intervention reduces distress and breathlessness, improves mood and increases mindfulness among hospital inpatients following acute exacerbation of COPD.Fifty patients were recruited following an acute admission. The immediate effects of a 10-minute mindfulness-based body scan were compared with a control intervention. Participants were randomized to receive either a mindfulness-based body scan (n = 24) or a control condition (n = 26) via a 10-minute audio recording. Participants completed a self-assessment survey, including the Borg scale for breathlessness, Philadelphia Mindfulness Scale and Hospital Anxiety and Depression Scale. They then completed six brief single item measures of dyspnoea, anxiety, depression, happiness, stress and mindfulness before and after the intervention daily for three consecutive days. Acceptability was rated according to ‘usefulness’ and whether they would recommend the intervention to other patients. Results showed that there was a tendency for change in most outcomes, but no significant differences between the groups. Most participants rated the intervention as useful and would recommend it. Existing knowledge of mindfulness interventions among these patients is very limited and this study may be helpful in the development of other brief interventions. © The Author(s) 2018. |
DOI Link: | 10.1177/1479972318766140 |
Rights: | This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
Licence URL(s): | http://creativecommons.org/licenses/by-nc/4.0/ |
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