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Senada Hajdarevic

senior lecturer, associate professor

Umea University

Sweden

Research Interests

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About

Senada Hajdarevic is a senior lecturer and associate professor at Umeå University in Sweden. Her research areas include eHealth literacy, chronic illness management, and the role of healthcare practitioners in cancer diagnosis and patient pathways. She has recently published articles focusing on qualitative studies in healthcare and the adaptation of health questionnaires to improve patient outcomes. Her work contributes significantly to the understanding of health-related internet use and the dynamics of clinical research nursing.

Articles (20)

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2026

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2022

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2020

Collaborators (14)

Michael Harris

University of Bath

UNITED KINGDOM

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Mercè Marzo‐Castillejo

Researcher

Institut Universitari d'Investigació en Atenció Primària Jordi Gol

SPAIN

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Tuomas Koskela

University of Tampere

FINLAND

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Kalle Grill

Associate Professor

Umea University

SWEDEN

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Anders Blomberg

Professor and Senior Consultant Physician

Umeå Universitet Medicinska fakulteten

SWEDEN

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Ulrika Öberg

Lecturer

Umeå Universitet Medicinska fakulteten

SWEDEN

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Anna-Britt Coe

Umea University

SWEDEN

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Åsa Hörnsten

Professor

Umeå Universitet Medicinska fakulteten

SWEDEN

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Bethany Van Guelpen

Umea University

SWEDEN

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Sara Lundell

Associate professor

Umeå University

SWEDEN

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Ulf Isaksson

Professor

Umeå Universitet Medicinska fakulteten

SWEDEN

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Davorina Petek

SLOVENIA

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Vija Silina

Acting Head of the Department

Riga Stradiņš University

LATVIA

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Peter Murchie

University of Aberdeen

UNITED KINGDOM

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Senada Hajdarevic

Research Interests

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About

Articles (20)

Primary healthcare providers’ strategies of handling patients presenting with potential cancer symptoms following the introduction of standardized cancer patient pathways in Sweden

NoRCa: a register-based data source for cancer research in northern Sweden

Psychometric testing of the 20-item Self-Management Assessment Scale in people with chronic obstructive pulmonary disease

Associations between self-conscious emotions and sociodemographic factors, lifestyle, burden of disease, and healthcare interventions: A cross-sectional study with people with chronic obstructive pulmonary disease

Becoming whole again—Caring for the self in chronic illness—A narrative review of qualitative empirical studies

Clinical research nurses perceive their role as being like the hub of a wheel without real power: Empirical qualitative research

Swedish translation and psychometric testing of the Self-Conscious Emotions in COPD Questionnaire

eHealth Literacy and Health-Related Internet Use Among Swedish Primary Health Care Visitors: Cross-Sectional Questionnaire Study

Why do European primary care physicians sometimes not think of, or act on, a possible cancer diagnosis?

The Swedish Version of the eHealth Literacy Questionnaire: Translation, Cultural Adaptation, and Validation Study

Reduction in the diagnostic interval after the introduction of cancer patient pathways for colorectal cancer in northern Sweden

What would primary care practitioners do differently after a delayed cancer diagnosis? Learning lessons from their experiences

Adopting standardized cancer patient pathways as a policy at different organizational levels in the Swedish Health System

Comparison of community health nurses' preventive home visits to older adults in Sweden and Slovenia:

Clarifying the role of clinical research nurses working in Sweden, using the Clinical Trial Nursing Questionnaire – Swedish version

Need of support perceived by patients primarily curatively treated for breast, colorectal, or prostate cancer and close to discharge from hospital—A qualitative study

Cancer Worry Distribution and Willingness to Undergo Colonoscopy at Three Levels of Hypothetical Cancer Risk—A Population-Based Survey in Sweden

Experiences of Online COVID-19 Information Acquisition among Persons with Type 2 Diabetes and Varying eHealth Literacy

A Focus Group Study of Perceptions of Genetic Risk Disclosure in Members of the Public in Sweden: “I’ll Phone the Five Closest Ones, but What Happens to the Other Ten?”

Public support for healthcare-mediated disclosure of hereditary cancer risk information: Results from a population-based survey in Sweden

Collaborators (14)

Michael Harris

Mercè Marzo‐Castillejo

Tuomas Koskela

Kalle Grill

Anders Blomberg

Ulrika Öberg

Anna-Britt Coe

Åsa Hörnsten

Bethany Van Guelpen

Sara Lundell

Ulf Isaksson

Davorina Petek

Vija Silina

Peter Murchie

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