Feasibility, Acceptability, and Potential Effectiveness of Dignity Therapy for People with Motor Neurone Disease

被引:43
|
作者
Bentley, Brenda [1 ]
O'Connor, Moira [1 ]
Kane, Robert [1 ]
Breen, Lauren J. [1 ]
机构
[1] Curtin Univ, Sch Psychol & Speech Pathol, Perth, WA 6845, Australia
来源
PLOS ONE | 2014年 / 9卷 / 05期
基金
澳大利亚研究理事会;
关键词
AMYOTROPHIC-LATERAL-SCLEROSIS; QUALITY-OF-LIFE; CLINICAL-SIGNIFICANCE; ASSISTED SUICIDE; PALLIATIVE CARE; TERMINALLY-ILL; ALS; END; EXPERIENCE; DISTRESS;
D O I
10.1371/journal.pone.0096888
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: Motor neurone disease (MND) practice guidelines suggest developing interventions that will promote hope, meaning, and dignity to alleviate psychological distress, but very little research has been done. This study begins to address this need by exploring the use of dignity therapy with people with MND. Dignity therapy is a brief psychotherapy that promotes hope, meaning and dignity, and enhances the end of life for people with advanced cancer. The aims of this study are to assess the feasibility, acceptability, and potential effectiveness of dignity therapy for people with MND. Methods/design: This cross-sectional feasibility study used a one-group pre-test post-test design with 29 people diagnosed with MND. Study participants completed the following self-report questionnaires: Herth Hope Index, FACIT-sp, Patient Dignity Inventory, ALS Assessment Questionnaire, ALS Cognitive Behavioural Screen, and a demographic and health history questionnaire. Acceptability was measured with a 25-item feedback questionnaire. Feasibility was assessed by examining the length of time taken to complete dignity therapy and how symptoms common in MND affected the intervention. Generalised linear mixed models and reliable change scores were used to analyse the data. Results: There were no significant pre-test post-test changes for hopefulness, spirituality or dignity on the group level, but there were changes in hopefulness on the individual level. The results of the feedback questionnaire indicates dignity therapy is highly acceptable to people with MND, who report benefits similar to those in the international randomised controlled trial on dignity therapy, a population who primarily had end-stage cancer. Benefits include better family relationships, improved sense of self and greater acceptance. Dignity therapy with people with MND is feasible if the therapist can overcome time and communication difficulties. Conclusions: Dignity therapy for people with MND is feasible and acceptable. Further research is warranted to explore its ability to diminish distress.
引用
收藏
页数:7
相关论文
共 50 条
  • [31] Telehealth dignity therapy for community-dwelling older adults: feasibility and potential efficacy
    Fallon, John
    Bhar, Sunil
    Quinn, Stephen
    JOURNAL OF POSITIVE PSYCHOLOGY, 2024, 19 (06) : 1109 - 1118
  • [32] The impact of communication on healthcare involvement for people living with motor neurone disease and their carers: A longitudinal qualitative study
    Paynter, Camille
    Mathers, Susan
    Gregory, Heidi
    Vogel, Adam P.
    Cruice, Madeline
    INTERNATIONAL JOURNAL OF LANGUAGE & COMMUNICATION DISORDERS, 2022, 57 (06) : 1318 - 1333
  • [33] National audit of cognitive assessment in people with pwMND A national audit of cognitive assessment in people with motor neurone disease (pwMND) in Scotland
    Stavrou, Maria
    Newton, Judith
    Stott, Gill
    Colville, Shuna
    Chandran, Siddharthan
    Abrahams, Sharon
    Pal, Suvankar
    Davenport, Richard
    AMYOTROPHIC LATERAL SCLEROSIS AND FRONTOTEMPORAL DEGENERATION, 2020, 21 (5-6) : 459 - 462
  • [34] Perceptions and experiences of control among people living with motor neurone disease: a systematic review and thematic synthesis
    Glennie, Nicola
    Harris, Fiona M.
    France, Emma F.
    DISABILITY AND REHABILITATION, 2023, 45 (16) : 2554 - 2566
  • [35] The need for support services for family carers of people with motor neurone disease (MND): views of current and former family caregivers a qualitative study
    O'Brien, Mary R.
    Whitehead, Bridget
    Jack, Barbara A.
    Mitchell, J. Douglas
    DISABILITY AND REHABILITATION, 2012, 34 (03) : 247 - 256
  • [36] Existential concerns for people with motor neurone disease: Who is listening to their needs, priorities and preferences?
    Harris, Denise A.
    BRITISH JOURNAL OF OCCUPATIONAL THERAPY, 2016, 79 (06) : 391 - 393
  • [37] How people with motor neurone disease talk about living with their illness: a narrative study
    Brown, Janice
    Addington-Hall, Julia
    JOURNAL OF ADVANCED NURSING, 2008, 62 (02) : 200 - 208
  • [38] Decision-Making for Gastrostomy and Ventilatory Support for People with Motor Neurone Disease: Variations across UK hospices
    Oliver, David
    Campbell, Colin
    Sykes, Nigel
    Tallon, Carole
    Edwards, Annette
    JOURNAL OF PALLIATIVE CARE, 2011, 27 (03) : 198 - 201
  • [39] Social services homecare for people with motor neurone disease/amyotrophic lateral sclerosis: Why are such services used or refused?
    O'Brien, Mary R.
    Whitehead, Bridget
    Murphy, Philip N.
    Mitchell, J. Douglas
    Jack, Barbara A.
    PALLIATIVE MEDICINE, 2012, 26 (02) : 123 - 131
  • [40] Implementation and evaluation of an education program to guide palliative care for people with motor neurone disease
    McConigley, Ruth
    Aoun, Samar
    Kristjanson, Linda
    Colyer, Sue
    Deas, Kathy
    O'Connor, Margaret
    Harris, Rod
    Currow, David
    Yates, Patsy
    PALLIATIVE MEDICINE, 2012, 26 (08) : 994 - 1000