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Izpis gradiva Pomoč

Naslov:Mapping users' experience of a family history and genetic risk algorithm tool in primary care
Avtorji:ID Miroševič, Špela (Avtor)
ID Krajc, Kaja (Avtor)
ID Klemenc-Ketiš, Zalika (Avtor)
ID Selič-Zupančič, Polona (Avtor)
Datoteke:.pdf Mirosevic-2021-Mapping_Users__Experience_of_a.pdf (361,59 KB)
MD5: A3246C1F892EEAFC870E46F44EE30788
 
URL https://doi.org/10.1159/000518086
 
Jezik:Angleški jezik
Vrsta gradiva:Znanstveno delo
Tipologija:1.01 - Izvirni znanstveni članek
Organizacija:MF - Medicinska fakulteta
Opis:Introduction: The development of a family history (FH) questionnaire (FHQ) provides an insight into a patient's familiarity of a trait and helps to identify individuals at increased risk of disease. A critical aspect of developing a new tool is exploring users' experience. Objective: The objective of this study was to examine users' experience, obstacles and challenges, and their views and concerns in the applicability of a new tool for determining genetic risk in Slovenia's primary care. Methods: We used a qualitative approach. The participants completed a risk assessment software questionnaire that calculates users' likelihood of developing familial diseases. Audio-taped semi-structured telephone interviews were conducted to evaluate their experience. There were 21 participants, and analyses using the constant comparative method were employed. Results: We identified 3 main themes: obstacles/key issues, suggestions for improvements, and coping. The participants were poorly satisfied with the clarity of instructions, technical usability problems, and issues with the entry of relatives' data. They expressed satisfaction with some of the characteristics of the FHQ (e.g., straightforward and friendly format, easy entry, and comprehension). They suggested simpler language, that the disease risk should be targeted toward the disease, that the FHQ should include patient-specific recommendations, and that it should be part of the electronic medical records. When discussing what would they do with the results of the FHQ, the participants used different coping strategies: active (e.g., seeking information) or passive (e.g., avoidance). Discussion/conclusion: User experience was shown to be a synthesis of obstacles, overcoming them with suggestions for improvements, and exploration of various coping mechanisms that may emerge from dealing with the stressor of "being at risk."
Ključne besede:primary healthcare, family history, qualitative methodology
Status publikacije:Objavljeno
Verzija publikacije:Objavljena publikacija
Poslano v recenzijo:04.03.2021
Datum sprejetja članka:22.06.2021
Datum objave:31.08.2022
Založnik:S. Karger
Leto izida:2022
Št. strani:Str. 42-51
Številčenje:Letn. 25, Št. 1/2
PID:20.500.12556/DKUM-90869 Novo okno
UDK:614
COBISS.SI-ID:76727555 Novo okno
DOI:10.1159/000518086 Novo okno
ISSN pri članku:1662-4246
Datum objave v DKUM:01.10.2024
Število ogledov:0
Število prenosov:2
Metapodatki:XML DC-XML DC-RDF
Področja:Ostalo
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Skupna ocena:(0 glasov)
Vaša ocena:Ocenjevanje je dovoljeno samo prijavljenim uporabnikom.
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Gradivo je del revije

Naslov:Public health genomics
Skrajšan naslov:Public health genomics
Založnik:S. Karger
ISSN:1662-4246
COBISS.SI-ID:514029081 Novo okno

Gradivo je financirano iz projekta

Financer:ARRS - Agencija za raziskovalno dejavnost Republike Slovenije
Številka projekta:L7-9414
Naslov:Razvoj algoritma za določanje genetskega tveganja na primarni ravni zdravstvenega varstva: novo orodje primarne preventive

Financer:ARRS - Agencija za raziskovalno dejavnost Republike Slovenije
Številka projekta:MR-39262

Licence

Licenca:CC BY 4.0, Creative Commons Priznanje avtorstva 4.0 Mednarodna
Povezava:http://creativecommons.org/licenses/by/4.0/deed.sl
Opis:To je standardna licenca Creative Commons, ki daje uporabnikom največ možnosti za nadaljnjo uporabo dela, pri čemer morajo navesti avtorja.
Začetek licenciranja:31.08.2021

Sekundarni jezik

Jezik:Slovenski jezik
Ključne besede:primarno zdravstveno varstvo, družinska zgodovina, kvalitativna metodologija


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