Literature DB >> 14586595

A disease-specific psychosocial questionnaire for Parkinson's disease caregivers.

Noëlle G A Spliethoff-Kamminga1, Aeilko H Zwinderman, Machiel P Springer, Raymund A C Roos.   

Abstract

OBJECTIVE: To evaluate the "Belastungsfragebogen Parkinson Angehörigen-kurzversion" (BELA-A-k), a questionnaire for measuring psychosocial problems and need for help in Parkinson's disease (PD) caregivers.
METHODS: The "Belastungsfragebogen Parkinson Angehörigen-kurzversion" was translated into Dutch. It consists of 15 items with a "Bothered by" (Bb) and a "Need for Help" (NfH) score. The BELA-A-k was tested for cultural differences, relevance and feasibility in a pilot (n = 10). We determined the psychometric properties in a validation study (n = 50) and compared the BELA-A-k with the Sickness Impact Profile, the COOP/WONCA Functional Health Assessment Charts and the Loneliness Questionnaire (de Jong-Gierveld). All questionnaires were administered in person at home, in a prescribed order.
RESULTS: The BELA-A-k was completed by 60 PD-caregivers. The internal-consistency reliability coefficients for the total "Bothered by" (0.90) and "Need for Help" (0.92) scales were excellent. The internal consistency of the subscales exceeded the 0.70 standard except for the "Bothered by" and "Need for Help" Social functioning scale (Bb = 0.62; NfH = 0.65) and the Partner-bonding/Family scale (NfH = 0.69). Almost all BELA-A-k subscales correlated highly (P < 0.001) with the corresponding scales of the standard quality of life indices.
CONCLUSION: The BELA-A-k is a relevant, reliable and valid measure for assessing psychosocial problems and need for help of PD-caregivers.

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Year:  2003        PMID: 14586595     DOI: 10.1007/s00415-003-0165-6

Source DB:  PubMed          Journal:  J Neurol        ISSN: 0340-5354            Impact factor:   4.849


  6 in total

1.  Burden of caregiving amongst family caregivers of patients with eating disorders.

Authors:  Angel Padierna; Josune Martín; Urko Aguirre; Nerea González; Pedro Muñoz; José Ma Quintana
Journal:  Soc Psychiatry Psychiatr Epidemiol       Date:  2012-06-22       Impact factor: 4.328

2.  Towards a better quality of life (QoL) for patients with pituitary diseases: results from a focus group study exploring QoL.

Authors:  Cornelie D Andela; Nicolasine D Niemeijer; Margreet Scharloo; Jitske Tiemensma; Shaaji Kanagasabapathy; Alberto M Pereira; Noëlle G A Kamminga; Ad A Kaptein; Nienke R Biermasz
Journal:  Pituitary       Date:  2015-02       Impact factor: 4.107

3.  Quality of life among caregivers of patients with eating disorders.

Authors:  Josune Martín; Angel Padierna; Urko Aguirre; José M Quintana; Carlota Las Hayas; Pedro Muñoz
Journal:  Qual Life Res       Date:  2011-03-04       Impact factor: 4.147

4.  Spanish version of the Parkinson's Disease Questionnaire-Carer (PDQ-Carer).

Authors:  Rosario Ferrer-Cascales; María José Cabañero-Martínez; Miriam Sánchez-SanSegundo; Nereida Congost-Maestre; Crispin Jenkinson
Journal:  Health Qual Life Outcomes       Date:  2016-11-04       Impact factor: 3.186

5.  Caregiver education in Parkinson's disease: formative evaluation of a standardized program in seven European countries.

Authors:  L E I A'Campo; N G A Spliethoff-Kamminga; M Macht; R A C Roos
Journal:  Qual Life Res       Date:  2009-11-28       Impact factor: 4.147

6.  Self-Management Education for Persons with Parkinson's Disease and Their Care Partners: A Quasi-Experimental Case-Control Study in Clinical Practice.

Authors:  Carina Hellqvist; Carina Berterö; Nil Dizdar; Märta Sund-Levander; Peter Hagell
Journal:  Parkinsons Dis       Date:  2020-04-30
  6 in total

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