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                  <mods:namePart>Marfil Gómez, Raquel</mods:namePart>
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                  <mods:namePart>Morales-Asencio, José Miguel</mods:namePart>
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                  <mods:namePart>Morilla-Herrera, Juan Carlos</mods:namePart>
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                  <mods:namePart>Martí-García, Celia</mods:namePart>
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                  <mods:namePart>López-Leiva, María Inmaculada</mods:namePart>
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                  <mods:namePart>García-Mayor, Silvia</mods:namePart>
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                  <mods:dateAccessioned encoding="iso8601">2025-09-03T11:49:42Z</mods:dateAccessioned>
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                  <mods:dateIssued encoding="iso8601">2020-10-15</mods:dateIssued>
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               <mods:identifier type="citation">Marfil-Gómez, R., Morales-Puerto, M., León-Campos, Á., Morales-Asencio, J. M., Morilla-Herrera, J. C., Timonet-Andreu, E., Cuevas-Fernández Gallego, M., Martí-García, C., López-Leiva, I., &amp; García-Mayor, S. (2020). Quality of Life, Physical and Mental Health of Family Caregivers of Dependent People with Complex Chronic Disease: Protocol of a Cohort Study. International Journal of Environmental Research and Public Health, 17(20), 7489. https://doi.org/10.3390/ijerph17207489</mods:identifier>
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               <mods:identifier type="doi">10.3390/ijerph17207489</mods:identifier>
               <mods:abstract>Abstract: Background: informal caregivers have a high risk of su ering from diseases derived&#xd;
from the chronic stress to which they are subjected for their dedication to the care of their relatives.&#xd;
Such stress has a direct influence on the person cared for, mainly a ecting the quality of their care.&#xd;
Therefore, the aim of the present study is to assess the association of caregiving on physical and&#xd;
mental perceived health in family caregivers of dependent adults with complex chronic diseases.&#xd;
Methods: a prospective longitudinal cohort study, with a follow-up period of 36 months (HUELLA&#xd;
cohort). The exposed cohort will be formed by family caregivers of dependent patients with complex&#xd;
chronic pathologies. The unexposed cohort will be taken from the general population adjusted for&#xd;
age, sex and health. Outcome variables will include attendance to health services, consumption of&#xd;
psychoactive drugs, dedication to care (only in exposed cohort), concession of the Act on Promotion&#xd;
of Personal Autonomy and Care for dependent persons (exposed only), perceived physical and&#xd;
mental health, depression level, burden level and new diagnosis of chronic pathology of the caregiver&#xd;
during the study. Results: the expected results will be applicable and will incorporate improvements&#xd;
to the usual health system clinical practice, providing feedback to professionals dedicated to the&#xd;
provision, planning and design of services to family caregivers, as well as to groups and organizations&#xd;
of caregivers. Conclusions: investments in preventing low-quality informal care are key, mainly&#xd;
through early identification and interventions to support caregivers who su er from stress, anxiety&#xd;
or depression.</mods:abstract>
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                  <mods:languageTerm authority="rfc3066">eng</mods:languageTerm>
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               <mods:accessCondition type="useAndReproduction">Attribution 4.0 Internacional</mods:accessCondition>
               <mods:subject>
                  <mods:topic>Cuidadores - Salud mental</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>Estrés (Psicología) - Control</mods:topic>
               </mods:subject>
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                  <mods:title>Quality of Life, Physical and Mental Health of Family Caregivers of Dependent People with Complex Chronic Disease: Protocol of a Cohort Study</mods:title>
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