<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-09-16T00:56:54Z</responseDate><request verb="GetRecord" identifier="oai:gredos.usal.es:10366/22617" metadataPrefix="dim">https://gredos.usal.es/oai/request</request><GetRecord><record><header><identifier>oai:gredos.usal.es:10366/22617</identifier><datestamp>2025-06-05T12:40:28Z</datestamp><setSpec>com_10366_4331</setSpec><setSpec>com_10366_4200</setSpec><setSpec>com_10366_3946</setSpec><setSpec>com_10366_3823</setSpec><setSpec>col_10366_4332</setSpec></header><metadata><dim:dim xmlns:dim="http://www.dspace.org/xmlns/dspace/dim" xmlns:doc="http://www.lyncode.com/xoai" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.dspace.org/xmlns/dspace/dim http://www.dspace.org/schema/dim.xsd">
<dim:field mdschema="dc" element="contributor" qualifier="author" lang="es_ES" authority="2193" confidence="500" orcid_id="">Rivera Navarro, Jesús</dim:field>
<dim:field mdschema="dc" element="contributor" qualifier="author" lang="es_ES" authority="10b4e813-1cc9-4a3e-adcb-0ca4bb646e79" confidence="500" orcid_id="">Morales González, José Manuel</dim:field>
<dim:field mdschema="dc" element="contributor" qualifier="author" lang="es_ES" authority="3da38448-1365-435a-a815-1538a4f9ee5f" confidence="500" orcid_id="">Benito-León, Julián</dim:field>
<dim:field mdschema="dc" element="contributor" qualifier="author" lang="es_ES" authority="c7a4d130-bb97-4497-9180-cb7a3b2327ad" confidence="500" orcid_id="">Grupo de Enfermedades Desmielinizantes de Madrid (España)</dim:field>
<dim:field mdschema="dc" element="date" qualifier="accessioned" lang="es_ES">2009-01-26</dim:field>
<dim:field mdschema="dc" element="date" qualifier="accessioned">2009-10-08T12:03:50Z</dim:field>
<dim:field mdschema="dc" element="date" qualifier="available">2009-10-08T12:03:50Z</dim:field>
<dim:field mdschema="dc" element="date" qualifier="issued" lang="es_ES">2003</dim:field>
<dim:field mdschema="dc" element="identifier" qualifier="citation" lang="es_ES">Rivera-Navarro, J., Morales González, J. M., Benito-León, J., y GEDMA (2003). Informal caregiving in multiple sclerosis patients : data from the Madrid demyelinating disease group study. "Disability and Rehabilitation, 25 (18), 1057-1064</dim:field>
<dim:field mdschema="dc" element="identifier" qualifier="uri">http://hdl.handle.net/10366/22617</dim:field>
<dim:field mdschema="dc" element="identifier" qualifier="doi">10.1080/0963828031000137766</dim:field>
<dim:field mdschema="dc" element="description" lang="es_ES">Se analizan los datos del Grupo de Enfermedades Desmielinizantes de pacientes con esclerosis múltiple</dim:field>
<dim:field mdschema="dc" element="description" qualifier="abstract" lang="es_ES">Purpose: To describe the profile of Multiple Sclerosis (MS) patient caregivers and assess their caregiving burden.Methods: A total of 91 MS patients, recruited from a Spanish longitudinal survey, and their corresponding caregivers were studied. Caregivers were administered a questionnaire thatcollected social and demographic data, and a generic caregiver burden interview (the Zarit scale). Furthermore, MS patientswere administered a specific health-related quality of life (HRQoL) instrument (the modified Spanish version of the Functional Assessment of Multiple Sclerosis).Results: 24.5% of the sample required caregivers to perform activities of daily life. Caregiver profile was as follows: 67%female; mean age, 51.5+14.1 years; and mean daily time devoted to care, 11.5+8.2 h. Most caregivers had some typeof support, 67% informal and 31.9% formal. The amount of time spent in caring for relatives was the main item determining the burden of MS-patient caregivers. Moreover, MS patient s HRQoL showed a moderate inverse correlation with caregiver burden.Conclusions: In contrast to previous studies, most Spanish MSpatientcaregivers are female, and there is a considerable percentage of parent caregivers. A greater degree of formalsupport and an improvement in MS patients  HRQoL may serve to reduce caregiver burden.</dim:field>
<dim:field mdschema="dc" element="format" qualifier="extent" lang="es_ES">8 p.</dim:field>
<dim:field mdschema="dc" element="format" qualifier="mimetype" lang="es_ES">application/pdf</dim:field>
<dim:field mdschema="dc" element="language" lang="es_ES">Inglés</dim:field>
<dim:field mdschema="dc" element="language" qualifier="iso" lang="es_ES">eng</dim:field>
<dim:field mdschema="dc" element="publisher" lang="es_ES">Taylor and Francis (Londres, Gran Bretaña)</dim:field>
<dim:field mdschema="dc" element="rights">Attribution-NonCommercial-NoDerivs 3.0 Unported</dim:field>
<dim:field mdschema="dc" element="rights" qualifier="uri">https://creativecommons.org/licenses/by-nc-nd/3.0/</dim:field>
<dim:field mdschema="dc" element="rights" qualifier="accessRights">info:eu-repo/semantics/embargoedAccess</dim:field>
<dim:field mdschema="dc" element="subject" lang="es_ES">Multiple sclerosis</dim:field>
<dim:field mdschema="dc" element="subject" lang="es_ES">Family</dim:field>
<dim:field mdschema="dc" element="subject" lang="es_ES">Esclerosis múltiple</dim:field>
<dim:field mdschema="dc" element="subject" qualifier="classification" lang="es_ES">Familia</dim:field>
<dim:field mdschema="dc" element="subject" qualifier="classification" lang="es_ES">Cuidadores</dim:field>
<dim:field mdschema="dc" element="title" lang="es_ES">Informal caregiving in multiple sclerosis patients : data from the Madrid demyelinating disease group study</dim:field>
<dim:field mdschema="dc" element="type" lang="es_ES">info:eu-repo/semantics/article</dim:field>
<dim:field mdschema="dc" element="type" lang="es_ES">info:eu-repo/semantics/article</dim:field>
<dim:field mdschema="dc" element="relation" qualifier="publishversion">https://doi.org/10.1080/0963828031000137766</dim:field>
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