Literature DB >> 18618351

Problem solving skills predict quality of life and psychological morbidity in ALS caregivers.

Virginia Murphy1, Stephanie H Felgoise, Susan M Walsh, Zachary Simmons.   

Abstract

Amyotrophic lateral sclerosis (ALS) often is associated with a particularly intensive caregiving experience, and the well-being of caregivers impacts that of patients. Thus, identification of factors leading to distress in caregivers may provide avenues for intervention that will help both the caregiver and the patient. We prospectively examined caregivers' social problem solving skills, the quality of the patient-caregiver relationship, caregivers' spirituality and religiousness, and the ways in which these impact caregivers' quality of life (QoL) and psychological morbidity in 75 caregivers of ALS patients. Data were analyzed through correlational and hierarchical multiple regression analyses. Social problem solving and spirituality were the best predictors of caregivers' QoL, accounting for 15.6% and 7.8% of the variance in QoL, respectively (F (2, 69) = 11.83, p<.001). Social problem solving also predicted and accounted for 25.4% of the variance in psychological morbidity (F (1, 71) = 25.571, p<.001). Level of care provided did not predict either QoL or psychological morbidity in caregivers. In conclusion, the problem-solving skills of ALS caregivers are an important determinant of caregiver well-being. Developing interventions to teach ALS caregivers effective methods of problem solving would probably be beneficial to this population.

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Year:  2009        PMID: 18618351     DOI: 10.1080/17482960802245007

Source DB:  PubMed          Journal:  Amyotroph Lateral Scler        ISSN: 1471-180X


  6 in total

1.  Ten years of riluzole use in a tertiary ALS clinic.

Authors:  Andrew Geronimo; Richard M Albertson; James Noto; Zachary Simmons
Journal:  Muscle Nerve       Date:  2022-04-13       Impact factor: 3.852

2.  Determinants of accepting non-invasive ventilation treatment in motor neurone disease: a quantitative analysis at point of need.

Authors:  Rosanna Cousins; Hikari Ando; Everard Thornton; Biswajit Chakrabarti; Robert Angus; Carolyn Young
Journal:  Health Psychol Behav Med       Date:  2013-11-01

3.  Lived Experience of Spouses of Persons with Motor Neuron Disease: Preliminary Findings through Interpretative Phenomenological Analysis.

Authors:  Manjusha G Warrier; Arun Sadasivan; Kiran Polavarapu; Veeramani Preethish Kumar; Niranjan Prakash Mahajan; Chevula Pradeep Chandra Reddy; Seena Vengalil; Saraswati Nashi; Atchayaram Nalini; Priya Treesa Thomas
Journal:  Indian J Palliat Care       Date:  2020-01-28

4.  A blended psychosocial support program for partners of patients with amyotrophic lateral sclerosis and progressive muscular atrophy: protocol of a randomized controlled trial.

Authors:  Jessica de Wit; Anita Beelen; Constance H C Drossaert; Ruud Kolijn; Leonard H van den Berg; Johanna M A Visser-Meily; Carin D Schröder
Journal:  BMC Psychol       Date:  2018-05-02

5.  Group interventions for amyotrophic lateral sclerosis caregivers in Ireland: a randomised controlled trial protocol.

Authors:  Tom Burke; Jennifer Wilson O'Raghallaigh; Sinead Maguire; Miriam Galvin; Mark Heverin; Orla Hardiman; Niall Pender
Journal:  BMJ Open       Date:  2019-09-20       Impact factor: 2.692

Review 6.  Support Needs and Interventions for Family Caregivers of Patients with Amyotrophic Lateral Sclerosis (ALS): A Narrative Review with Report of Telemedicine Experiences at the Time of COVID-19 Pandemic.

Authors:  Giulia D'Alvano; Daniela Buonanno; Carla Passaniti; Manuela De Stefano; Luigi Lavorgna; Gioacchino Tedeschi; Mattia Siciliano; Francesca Trojsi
Journal:  Brain Sci       Date:  2021-12-30
  6 in total

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