Evidence map›Paper›PMID 35525943›Full record

ArticleHealth and quality of life outcomes2022

Listening to families with a person with neurodegenerative disease talk about their quality of life: integrating quantitative and qualitative approaches.

Alba Aza, María Gómez-Vela, Marta Badia, M Begoña Orgaz, Eva González-Ortega, Isabel Vicario-Molina, Estrella Montes-López

Abstract read
In one paragraph

Article in Health and quality of life outcomes, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Necropolitics of Death in Neurodegeneration.Culture, medicine and psychiatry · 2024
    Review
  6. Article
  7. Review
  8. Article
  9. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Alba AzaInstitute on Community Integration (INICO), Faculty of Psychology, University of Salamanca, Avda. De la Merced, 109-131, 37005, Salamanca, Castile and Leon, Spain. azhernandez@usal.es.ORCID https://orcid.org/0000-0002-1460-1195
María Gómez-VelaInstitute on Community Integration (INICO), Faculty of Education, University of Salamanca, Salamanca, Spain.
Marta BadiaInstitute on Community Integration (INICO), Faculty of Psychology, University of Salamanca, Avda. De la Merced, 109-131, 37005, Salamanca, Castile and Leon, Spain.ORCID https://orcid.org/0000-0001-6358-8057
M Begoña OrgazInstitute on Community Integration (INICO), Faculty of Psychology, University of Salamanca, Avda. De la Merced, 109-131, 37005, Salamanca, Castile and Leon, Spain.ORCID https://orcid.org/0000-0003-2244-6321
Eva González-OrtegaTeacher Training College of Zamora, University of Salamanca, Zamora, Spain.ORCID https://orcid.org/0000-0003-2244-895X
Isabel Vicario-MolinaTeacher Training College of Zamora, University of Salamanca, Zamora, Spain.ORCID https://orcid.org/0000-0002-5097-9195
Estrella Montes-LópezDepartment of Sociology and Communication, Faculty of Social Sciences, University of Salamanca, Salamanca, Spain.ORCID https://orcid.org/0000-0002-8226-7504

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe diagnosis of a neurodegenerative disease (ND) produces profound changes in the quality of life of the affected families. Despite the vital importance of these processes, the scientific literature has addressed this topic almost exclusively relating to the main caregiver or using limited approaches. Thus, the main objective of this research is to achieve a deeper understanding of the quality of family life of people with a neurodegenerative disease, following a mixed-method approach that combines quantitative and qualitative methodology.

methodsThe quantitative instrument was the Spanish version of the Family Quality of Life Survey-Neurodegenerative Disease (FQOLS-ND), which was completed by 300 participating families. The qualitative methodology was used in two focus groups with family caregivers, with a total of 21 participants.

resultsOn the one hand, confirmation of the dimensional structure of the scale in the focus groups was obtained and, on the other hand, the results of family quality of life in attainment and satisfaction were shown to be high for Family Relations and Careers and Planning for Careers and low for Support from Services and Leisure and Recreation.

conclusionsThe results of this study, through the combination of quantitative and qualitative information, helps to identify key issues to optimize services that respond to the priority needs of families.

Indexed as

Neurodegenerative DiseasesQuality of LifeCaregiversFamilyHumansFamily Quality of LifeFocus groupsFQoLS-NDNeurodegenerative diseases

Identifiers

PMID35525943
PMCPMC9077340

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.