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      <dc:title>Psychological distress in relatives undergoing familial screening for hypertrophic or dilated cardiomyopathy: a prospective longitudinal observational cohort study</dc:title>
      <dc:creator>Puig Torrens, Júlia</dc:creator>
      <dc:subject>Cardiopatia congènita</dc:subject>
      <dc:subject>Congenital heart disease</dc:subject>
      <dc:subject>Cor -- Malalties -- Aspectes genètics</dc:subject>
      <dc:subject>Heart -- Diseases -- Genetic aspects</dc:subject>
      <dc:subject>Cribratge genètic -- Aspectes psicològics</dc:subject>
      <dc:subject>Genetic screening -- Psychological aspects</dc:subject>
      <dc:subject>Pacients -- Satisfacció</dc:subject>
      <dc:subject>Patient satisfaction</dc:subject>
      <dc:subject>Cor -- Malalties -- Detecció precoç</dc:subject>
      <dc:subject>Heart -- Diseases -- Early detection</dc:subject>
      <dc:description>BACKGROUND: Inherited cardiomyopathies, such as hypertrophic cardiomyopathy (HCM) and dilated (DCM) cardiomyopathy, can present with a wide range of symptoms and in some occasions lead to sudden cardiac death (SCD) in young individuals. Familial screening enables early identification of at-risk relatives, enabling prevention and improving clinical management. While the psychological burden of affected individuals has been well documented, the emotional impact of screening of at-risk asymptomatic relatives requires additional evaluation. Understanding the psychological responses to screening is essential for optimizing genetic counseling and psychological support for families.&#xd;
OBJECTIVE: To evaluate the psychological distress associated with familial cardiomyopathy screening, examining differences between gene-positive and gene-elusive families and changes over a one-year period.&#xd;
DESIGN: Prospective, longitudinal, observational cohort study conducted at the Familial Cardiomyopathies Unit, Hospital Universitari de Girona Dr. Josep Trueta over a 3-year period. The current study encompasses (1) a cross-sectional comparison of emotional distress at baseline between relatives belonging to gene-positive and gene-elusive families, and (2) a longitudinal evaluation of changes in distress after one-year of follow-up.&#xd;
PARTICIPANTS: Asymptomatic adult relatives of index patients diagnosed with HCM or DCM, recruited consecutively at their first visit for family screening.&#xd;
METHODS: A total of 168 participants will be recruited and divided into two subgroups based on family genetic status: gene-positive gene-elusive families. Psychological distress will be measured using the Hospital Anxiety and Depression Scale (HADS) at three time points: baseline (T0), immediately after disclosure of genetic results (Tg, for those belonging to gene-positive families only), and one-year follow-up (T1). Data will be recorded in an electronic Case Report Form and analyzed using descriptive and inferential statistics</dc:description>
      <dc:description>3</dc:description>
      <dc:date>2026-04-18T21:02:24Z</dc:date>
      <dc:date>2026-04-18T21:02:24Z</dc:date>
      <dc:date>2025-11</dc:date>
      <dc:type>info:eu-repo/semantics/bachelorThesis</dc:type>
      <dc:identifier>https://hdl.handle.net/10256/28678</dc:identifier>
      <dc:rights>Attribution-NonCommercial-NoDerivatives 4.0 International</dc:rights>
      <dc:rights>http://creativecommons.org/licenses/by-nc-nd/4.0/</dc:rights>
      <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
      <dc:coverage>east=2.8199565410614014; north=41.99757439066319; name=Hospital Universitari de Girona Dr. Josep Trueta</dc:coverage>
      <dc:source>Medicina (TFG)</dc:source>
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