Literature DB >> 27385055

Improving the quality of life and psychological well-being of recently diagnosed multiple sclerosis patients: preliminary evaluation of a group-based cognitive behavioral intervention.

Emanuela Calandri1, Federica Graziano2, Martina Borghi2,3, Silvia Bonino1,2.   

Abstract

PURPOSE: The study evaluated a group-based cognitive behavioral intervention aimed at promoting the quality of life and the psychological well-being of recently diagnosed multiple sclerosis (MS) patients (up to 3 years since the diagnosis).
METHOD: The study involved 85 patients [59% women; mean age 37, SD = 12.3; 94% with relapsing-remitting MS; Expanded Disability Status Scale (EDSS) between 1 and 4]. A quasi-experimental study design was applied; 54 patients (intervention group) participated in five group sessions, a 6-month post-intervention and a 1-year follow-up; 31 patients (comparison group) participated in activities routinely provided to recently diagnosed MS patients. Measures of Quality of Life (SF-12), Depression (CESD-10), Affective well-being (PANAS) and Optimism (LOT-R) were assessed.
RESULTS: At the 6-month post-intervention, mental health increased in the intervention group and decreased in the comparison group, whereas negative affect decreased in the intervention group and increased in the comparison group. At the 1-year follow-up, mental health and optimism increased in the intervention group and decreased in the comparison group.
CONCLUSIONS: Preliminary evidence suggests that the proposed intervention fosters the quality of life and the psychological well-being of recently diagnosed MS patients by reducing negative affect and promoting mental health and optimism, particularly in the long term. Implications for Rehabilitation Preliminary evidence suggests that a group-based cognitive behavioral intervention focused on identity redefinition, sense of coherence and self-efficacy promotes the quality of life (increased mental health) and psychological well-being (decreased negative affect and increased optimism) of recently diagnosed MS patients (up to 3 years since the diagnosis). The first years following the MS diagnosis should be considered a good time for a psychological intervention aimed at promoting the patient's adjustment to the illness. Strategies should be found to increase the participation of recently diagnosed MS patients in psychological interventions.

Entities:  

Keywords:  Chronic illness; depression; empowerment; mental health; optimism; positive and negative affect

Mesh:

Year:  2016        PMID: 27385055     DOI: 10.1080/09638288.2016.1198430

Source DB:  PubMed          Journal:  Disabil Rehabil        ISSN: 0963-8288            Impact factor:   3.033


  8 in total

1.  Health outcomes and adherence to a healthy lifestyle after a multimodal intervention in people with multiple sclerosis: Three year follow-up.

Authors:  Claudia H Marck; Alysha M De Livera; Chelsea R Brown; Sandra L Neate; Keryn L Taylor; Tracey J Weiland; Emily J Hadgkiss; George A Jelinek
Journal:  PLoS One       Date:  2018-05-23       Impact factor: 3.240

2.  Distress and risk perception in people living with multiple sclerosis during the early phase of the COVID-19 pandemic.

Authors:  Kevin N Alschuler; Michelle K Roberts; Tracy E Herring; Dawn M Ehde
Journal:  Mult Scler Relat Disord       Date:  2020-11-05       Impact factor: 4.339

3.  Quality of life in adults with multiple sclerosis: a systematic review.

Authors:  Irene Gil-González; Agustín Martín-Rodríguez; Rupert Conrad; María Ángeles Pérez-San-Gregorio
Journal:  BMJ Open       Date:  2020-11-30       Impact factor: 2.692

4.  The impact of cognitive rehabilitation on quality of life in multiple sclerosis: A pilot study.

Authors:  Kathleen C Munger; Amy Pacos Martinez; Megan H Hyland
Journal:  Mult Scler J Exp Transl Clin       Date:  2021-08-26

5.  Psychosocial interventions for adults with newly diagnosed chronic disease: A systematic review.

Authors:  Samuel Akyirem; Angus Forbes; Julie Lindberg Wad; Mette Due-Christensen
Journal:  J Health Psychol       Date:  2021-02-14

6.  The impact of self-perceived limitations, stigma and sense of coherence on quality of life in multiple sclerosis patients: results of a cross-sectional study.

Authors:  Feddrik Broersma; Barth Oeseburg; Jacob Dijkstra; Klaske Wynia
Journal:  Clin Rehabil       Date:  2017-09-12       Impact factor: 3.477

7.  Biopsychosocial model of resilience in young adults with multiple sclerosis (BPS-ARMS): an observational study protocol exploring psychological reactions early after diagnosis.

Authors:  Alberto Gajofatto; Valeria Donisi; Isolde Martina Busch; Francesca Gobbin; Elena Butturini; Massimiliano Calabrese; Alessandra Carcereri de Prati; Paola Cesari; Lidia Del Piccolo; Massimo Donadelli; Paolo Fabene; Stefania Fochi; Macarena Gomez-Lira; Roberta Magliozzi; Giovanni Malerba; Raffaella Mariotti; Sofia Mariotto; Chiara Milanese; Maria Grazia Romanelli; Andrea Sbarbati; Federico Schena; Maria Angela Mazzi; Michela Rimondini
Journal:  BMJ Open       Date:  2019-08-02       Impact factor: 2.692

8.  Evaluation of cognitive rehabilitation on the cognitive performance in multiple sclerosis: A randomized controlled trial.

Authors:  Mohammad Mahdi Shahpouri; Majid Barekatain; Mahgol Tavakoli; Shahin Sanaei; Vahid Shaygannejad
Journal:  J Res Med Sci       Date:  2019-12-23       Impact factor: 1.852

  8 in total

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