Literature DB >> 18785883

Psychosocial interventions for non-professional carers of people with Parkinson's disease: a systematic scoping review.

Susanne Hempel1, Gill Norman, Su Golder, Raquel Aguiar-Ibáñez, Alison Eastwood.   

Abstract

AIM: This paper is a report of a scoping review to systematically identify and collate the evidence on psychosocial interventions for non-professional carers of people with Parkinson's disease.
BACKGROUND: Carers are critical to people with Parkinson's disease maintaining independent living and quality of life. Parkinson's disease imposes a challenging constellation of symptoms and no summary of effective interventions for carers and their unique support needs exists. DATA SOURCES: Thirty electronic databases were searched from their inception to July 2006, and bibliographies and specific internet sites were scanned.
METHODS: Eligible studies were categorized according to design, type of economic evaluation where applicable, number of participants, country of evaluation, intervention, orientation, provider, setting, method of delivery, carer population, patient population, carer outcomes, patient outcomes and authors' conclusions. Data were extracted by one reviewer and checked by another reviewer; discrepancies were resolved through discussion or arbitration by a third reviewer.
FINDINGS: Thirty studies met the inclusion criteria. Most investigated relatively unique interventions involving multiple elements; the majority were not aimed primarily at carers but were embedded in patient treatment programmes. Many were pilot studies, employing weak research designs and involving very small numbers of participants and most were not designed to assess the clinical or cost effectiveness of the intervention for the carers.
CONCLUSION: Several interventions merit further investigation but there is currently little evidence to show which approaches are effective and cost effective in supporting carers. Future studies need to employ appropriate and rigorous research designs with adequate samples and outcome measures, and with more focus on the carer.

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Year:  2008        PMID: 18785883     DOI: 10.1111/j.1365-2648.2008.04806.x

Source DB:  PubMed          Journal:  J Adv Nurs        ISSN: 0309-2402            Impact factor:   3.187


  6 in total

1.  Palliative Care and Parkinson's Disease: Caregiver Perspectives.

Authors:  Isabel Boersma; Jacqueline Jones; Christina Coughlan; Julie Carter; David Bekelman; Janis Miyasaki; Jean Kutner; Benzi Kluger
Journal:  J Palliat Med       Date:  2017-05-18       Impact factor: 2.947

2.  Close relationships in Parkinson´s disease patients with device-aided therapy.

Authors:  Monica Scharfenort; Jonathan Timpka; Thomas Sahlström; Tove Henriksen; Dag Nyholm; Per Odin
Journal:  Brain Behav       Date:  2021-05-05       Impact factor: 2.708

3.  Role of family caregivers regarding sexual and reproductive health for women and girls with intellectual disability: A scoping review.

Authors:  R M Powell; S L Parish; M Mitra; E Rosenthal
Journal:  J Intellect Disabil Res       Date:  2019-12-05

Review 4.  Understanding the Burden on Caregivers of People with Parkinson's: A Scoping Review of the Literature.

Authors:  Rozina Bhimani
Journal:  Rehabil Res Pract       Date:  2014-09-14

Review 5.  Social Determinants of Health: Underreported Heterogeneity in Systematic Reviews of Caregiver Interventions.

Authors:  Heather M Young; Janice F Bell; Robin L Whitney; Ronit A Ridberg; Sarah C Reed; Peter P Vitaliano
Journal:  Gerontologist       Date:  2020-02-14

Review 6.  Report from a multidisciplinary meeting on anxiety as a non-motor manifestation of Parkinson's disease.

Authors:  Gregory M Pontone; Nadeeka Dissanayka; Liana Apostolova; Richard G Brown; Roseanne Dobkin; Kathy Dujardin; Joseph H Friedman; Albert F G Leentjens; Eric J Lenze; Laura Marsh; Lynda Mari; Oury Monchi; Irene H Richard; Anette Schrag; Antonio P Strafella; Beth Vernaleo; Daniel Weintraub; Zoltan Mari
Journal:  NPJ Parkinsons Dis       Date:  2019-12-11
  6 in total

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