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A Qualitative Exploration of Ethical Aspects of Using AI in Parkinson Disease: Patient Panel Study

Luckhaus, Jamie Linnea; Scott Duncan, Therese; Kharko, Anna; Clareborn, Anna et al.

Ingår i JMIR AI, 2026

• DOI för A Qualitative Exploration of Ethical Aspects of Using AI in Parkinson Disease: Patient Panel Study
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Acceptable accuracy for medical AI: a survey of physicians and the general population in Sweden

Arvidsson, Rasmus; Widen, Jonathan; Al-Naasan, Lina; Gunnarsson, Ronny Kent K. et al.

Ingår i BMJ Health & Care Informatics, 2026

• DOI för Acceptable accuracy for medical AI: a survey of physicians and the general population in Sweden
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Adoption and Use of Proxy Online Record Access in Sweden – A Retrospective Analysis

Hägglund, Maria; Kharko, Anna; Riggare, Sara; Blease, Charlotte et al.

Ingår i Studies in Health Technology and Informatics, s. 1900-1904, 2026

• DOI för Adoption and Use of Proxy Online Record Access in Sweden – A Retrospective Analysis

AI-baserad rörelsemonitorering i patientrum: En studie om implementering av AI-teknik och vidareutveckling

Nilsson, Astrid; Norell, Emma

2026

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Ambient AI in primary care: an exploratory mixed methods survey of UK general practitioners

Blease, Charlotte; Kharko, Anna; Garcia Sanchez, Carolina; Navarro, David et al.

Ingår i BMJ Health & Care Informatics, 2026

• DOI för Ambient AI in primary care: an exploratory mixed methods survey of UK general practitioners
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Centralt- eller verksamhetsägd medicinteknisk utrustning?: En utredning av centralägd och verksamhetsägd medicinteknisk utrustning i Sverige

Gauffin, Andrea Carmel; Thorsten, Albin

2026

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"ChatGPT knows my Parkinson's": Perspectives of people with Parkinson's disease on use of generative AI.

Luckhaus, Jamie; Kharko, Anna; Scott Duncan, Therese; Riggare, Sara et al.

Ingår i Journal of Parkinson's Disease, 2026

• DOI för "ChatGPT knows my Parkinson's": Perspectives of people with Parkinson's disease on use of generative AI.

Comparing Stakeholders’ Perspectives on Parkinson Disease Management and Digital Technologies: Exploratory International Survey

Luckhaus, Jamie; Kharko, Anna; Blease, Charlotte; Almarcha-Menargues, Maria-Luisa et al.

Ingår i JMIR Formative Research, 2026

• DOI för Comparing Stakeholders’ Perspectives on Parkinson Disease Management and Digital Technologies: Exploratory International Survey
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Coproduction Without Youth?: Closing the Participation Gap in Digital Mental Health Research

Blease, Charlotte; Tibbs, Maria; Balaskas, Andreas; Liverpool, Shaun et al.

Ingår i JMIR Mental Health, 2026

• DOI för Coproduction Without Youth?: Closing the Participation Gap in Digital Mental Health Research
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Development and pilot feasibility of Kit-CAT, a serious-game-supported consultation for discussing complementary and alternative therapies in breast cancer care

Pinsault, Nicolas; Girard, Pauline; Monvoisin, Richard; Eychenne, Claire et al.

Ingår i Cancer Treatment and Research Communications, 2026

• DOI för Development and pilot feasibility of Kit-CAT, a serious-game-supported consultation for discussing complementary and alternative therapies in breast cancer care
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Diagnostic delay, care needs, and trust in healthcare among persons with rare disease and their next of kin living in Sweden

Soller, Maria Johansson; Luckhaus, Jamie Linnea; Juran, Stephanie; Ingvoldstad Malmgren, Charlotta

Ingår i Journal of Community Genetics, 2026

• DOI för Diagnostic delay, care needs, and trust in healthcare among persons with rare disease and their next of kin living in Sweden
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Digital vård i hemmet: En studie inom region Dalarnas pilotprojekt om egenmonitorering

Djerf, Cecilia

2026

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Editorial: Pushing boundaries in EHR implementation and innovation through advanced digital health technologies

Piho, Gunnar; Krastev, Evgeniy; Peltonen, Laura-Maria; Hägglund, Maria et al.

Ingår i Frontiers in Medicine, 2026

• DOI för Editorial: Pushing boundaries in EHR implementation and innovation through advanced digital health technologies
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Epistemic agency in self-tracking: a conceptual literature review of quantified self as citizen science for health

Riggare, Sara; Blomseth Christiansen, Thomas; Eg Larsen, Jakob; Jonas, Steven et al.

Ingår i Frontiers in Public Health, 2026

• DOI för Epistemic agency in self-tracking: a conceptual literature review of quantified self as citizen science for health
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Errors in AI-Transformed Patient-Centered Mental Health Documentation Written by Psychiatrists: Qualitative Pre-Post Study

Menekseoglu, Pelin Ozkara; Weibezahl, Mareike; Ellingsen, Mats; Sterkenburg, Jarl et al.

Ingår i JMIR Mental Health, 2026

• DOI för Errors in AI-Transformed Patient-Centered Mental Health Documentation Written by Psychiatrists: Qualitative Pre-Post Study
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Errors That Matter: Negative Experiences of Incorrect and Incomplete Health Records Among Youth in Mental Healthcare

Hagström, Josefin; Hägglund, Maria; Blease, Charlotte; Kharko, Anna

Ingår i Studies in Health Technology and Informatics, s. 1865-1869, 2026

• DOI för Errors That Matter: Negative Experiences of Incorrect and Incomplete Health Records Among Youth in Mental Healthcare

Failed Implementation of Mobile Access to Electronic Health Records in Home Care: Qualitative Study in Sweden

Jäderlund Hagstedt, Lovisa; Hvitfeldt, Helena; Hägglund, Maria

Ingår i JMIR mhealth and uhealth, 2026

• DOI för Failed Implementation of Mobile Access to Electronic Health Records in Home Care: Qualitative Study in Sweden
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Gender by Design: Visual Communication in Digital Health Platforms for Women’s Health

Terceiro, Luciana; Hägglund, Maria; Kharko, Anna

Ingår i International Conference on Human-Computer Interaction, s. 268-281, 2026

Good knowledge, poor behaviour?: Pelvic floor understanding and continence practices related to continence in nulliparous women in France

Dalla Serra, Aurore; Longsworth, Sara Eve Graham; Druart, Leo

Ingår i FRENCH JOURNAL OF UROLOGY, 2026

• DOI för Good knowledge, poor behaviour?: Pelvic floor understanding and continence practices related to continence in nulliparous women in France
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Has anything changed for Fibromyalgia?: Focus groups with patients on their lived experiences in England

Locher, Cosima; Kharko, Anna; Lanario, Joseph W.; Druart, Leo et al.

Ingår i PLOS ONE, 2026

• DOI för Has anything changed for Fibromyalgia?: Focus groups with patients on their lived experiences in England
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Health Care Professionals’ and Patients’ Perceptions and Experiences of Who Uses Video Consultations, and Why: Qualitative Study

Muli, Irene; Cajander, Åsa; Davoody, Nadia; Hagstedt, Lovisa Jäderlund et al.

Ingår i JMIR Human Factors, 2026

• DOI för Health Care Professionals’ and Patients’ Perceptions and Experiences of Who Uses Video Consultations, and Why: Qualitative Study
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How clinicians explain a diagnosis of functional neurological disorder: A qualitative study with general practitioners, neurologists, psychologists and physiotherapists

Marchica, E.; Vercueil, L.; Druart, Leo

Ingår i Revue Neurologique, s. 280-289, 2026

• DOI för How clinicians explain a diagnosis of functional neurological disorder: A qualitative study with general practitioners, neurologists, psychologists and physiotherapists
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Investigating Placebos and Controls Used in Large Language Model-Based Chatbot Intervention Trials: Protocol for a Methodological Review

Druart, Leo; Faria, Vanda; Annoni, Marco; Torous, John et al.

Ingår i JMIR Research Protocols, 2026

• DOI för Investigating Placebos and Controls Used in Large Language Model-Based Chatbot Intervention Trials: Protocol for a Methodological Review

Making patient experience actionable: applying importance-performance analysis to guide improvements in Swedish healthcare

Scott Duncan, Therese; Lind, Louise; Aslund, Li; Dieker, Eva et al.

Ingår i Frontiers in Health Services, 2026

• DOI för Making patient experience actionable: applying importance-performance analysis to guide improvements in Swedish healthcare
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Mapping Existing Evidence on Physicians’ and Patients’ Experiences with GenAI in Clinical Communication and Documentation: A Rapid Review

Garcia Sanchez, Carolina; Kharko, Anna; Hägglund, Maria; Riggare, Sara et al.

Ingår i Studies in Health Technology and Informatics, s. 675-679, 2026

• DOI för Mapping Existing Evidence on Physicians’ and Patients’ Experiences with GenAI in Clinical Communication and Documentation: A Rapid Review

“More than a pretty face”: Graphic User Interface Rubric for Assessment of Digital Health Platforms

Terceiro, Luciana; Hägglund, Maria; Kharko, Anna

Ingår i Studies in Health Technology and Informatics, s. 1814-1815, 2026

• DOI för “More than a pretty face”: Graphic User Interface Rubric for Assessment of Digital Health Platforms

Multidisciplinary research priorities for artificial intelligence in mental health: a call to action

Linardon, Jake; Firth, Joseph; Carvalho, Andre F.; Bockting, Claudi L. et al.

Ingår i Lancet psychiatry, s. 792-803, 2026

• DOI för Multidisciplinary research priorities for artificial intelligence in mental health: a call to action
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Nationwide Digital Integrated Care Plan for Coordinated Health and Social Services – An Estonian Example

Dudkina, Anna; Lubi, Kadi; Gross-Paju, Katrin; Scott Duncan, Therese et al.

Ingår i Studies in Health Technology and Informatics, 2026

• DOI för Nationwide Digital Integrated Care Plan for Coordinated Health and Social Services – An Estonian Example

Patient and Family Perspectives on Generative AI Tools in Rare Diseases: Exploratory Mixed Methods Online Survey

Blease, Charlotte; Jones, James; Blease, Catherine E.; Kharko, Anna et al.

Ingår i Journal of Participatory Medicine, 2026

• DOI för Patient and Family Perspectives on Generative AI Tools in Rare Diseases: Exploratory Mixed Methods Online Survey
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Patient Rights to Correct Errors in the Electronic Health Record: Comparison of Legislation in Sweden, UK, and Germany

Kharko, Anna; Blease, Charlotte; Hagström, Josefin; Schreiweis, Björn et al.

Ingår i Studies in Health Technology and Informatics, s. 1710-1714, 2026

• DOI för Patient Rights to Correct Errors in the Electronic Health Record: Comparison of Legislation in Sweden, UK, and Germany
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Patients' and Health Care Professionals' Experiences of a Digital Self-Management System for Asthma: Qualitative Study

Jäderlund Hagstedt, Lovisa; Hvitfeldt, Helena; Riggare, Sara; Petersson, Göran et al.

Ingår i JMIR Human Factors, 2026

• DOI för Patients' and Health Care Professionals' Experiences of a Digital Self-Management System for Asthma: Qualitative Study
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Patients are disclosing sensitive information to AI tools: clinicians must adapt

Blease, Charlotte

Ingår i The BMJ, 2026

• DOI för Patients are disclosing sensitive information to AI tools: clinicians must adapt

Playing for Keeps: Long‐Term Recall With an Application Using Virtual Reality and the Method of Loci

Hagström, Josefin; Winman, Anders

Ingår i Scandinavian Journal of Psychology, 2026

• DOI för Playing for Keeps: Long‐Term Recall With an Application Using Virtual Reality and the Method of Loci

Primary and secondary patient participation - a qualitative study of healthcare professionals’ perceptions and experiences

Scott Duncan, Therese; Wannheden, Carolina; Hägglund, Maria; Koch, Sabine et al.

Ingår i BMC Health Services Research, 2026

• DOI för Primary and secondary patient participation - a qualitative study of healthcare professionals’ perceptions and experiences
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Psychiatrists' experiences and opinions of generative AI: An exploratory online mixed methods survey in Germany

Schwarz, Julian; Goer, Vera; Guzhova, Olga; Holtz, Lena et al.

Ingår i Digital Health, 2026

• DOI för Psychiatrists' experiences and opinions of generative AI: An exploratory online mixed methods survey in Germany
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Quality in Use in Connected Mental Health: Protocol for a Systematic Mapping Study

Premanandan, Shweta; Ouhbi, Sofia; Ramstedt Stadin, Magdalena; Blease, Charlotte et al.

Ingår i JMIR Research Protocols, 2026

• DOI för Quality in Use in Connected Mental Health: Protocol for a Systematic Mapping Study
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Re-visiting professional ethics in psychotherapy: reflections on the use of talking therapies as a supportive adjunct for myalgic encephalomyelitis/chronic fatigue syndrome and ‘medically unexplained symptoms’

Hunt, Joanne; Blease, Charlotte

Ingår i Journal of Medical Ethics, s. 472-480, 2026

• DOI för Re-visiting professional ethics in psychotherapy: reflections on the use of talking therapies as a supportive adjunct for myalgic encephalomyelitis/chronic fatigue syndrome and ‘medically unexplained symptoms’
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"The more you learn, the more you can influence" — learning circles to support citizen science in Parkinson's disease: a pilot study in Sweden

Luckhaus, Jamie Linnea; Scott Duncan, Therese; Hellqvist, Carina; Riggare, Sara

Ingår i Frontiers in Public Health, 2026

• DOI för "The more you learn, the more you can influence" — learning circles to support citizen science in Parkinson's disease: a pilot study in Sweden
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Understanding disability/impairment, inclusively: the case of myalgic encephalomyelitis/chronic fatigue syndrome

Hunt, Joanne

Ingår i Disability & Society, s. 281-287, 2026

• DOI för Understanding disability/impairment, inclusively: the case of myalgic encephalomyelitis/chronic fatigue syndrome
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Understanding Patient-Reported Offenses in Electronic Health Records: Cross-Sectional Mixed Methods Survey

Simola, Saija; Kujala, Sari; Cajander, Åsa; Kharko, Anna et al.

Ingår i Journal of Medical Internet Research, 2026

• DOI för Understanding Patient-Reported Offenses in Electronic Health Records: Cross-Sectional Mixed Methods Survey

Use of ambient AI scribe in physicians' clinical documentation: a protocol for a systematic review on effectiveness, efficiency, and satisfaction.

Garcia Sanchez, Carolina; Goer, Vera; Kharko, Anna; Hägglund, Maria et al.

Ingår i BMJ Open, 2026

• DOI för Use of ambient AI scribe in physicians' clinical documentation: a protocol for a systematic review on effectiveness, efficiency, and satisfaction.
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What do patients consider sensitive health information?: A cross-sectional survey of national patient portal users

Simola, Saija; Kujala, Sari; Kharko, Anna; Hagström, Josefin et al.

Ingår i Digital Health, s. 1-19, 2026

• DOI för What do patients consider sensitive health information?: A cross-sectional survey of national patient portal users
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Will AI do more harm than good to the UK's mental health?

McGilchrist, Iain; Osler, Lucy; Blease, Charlotte

Ingår i BMJ British Medical Journal, 2026

• DOI för Will AI do more harm than good to the UK's mental health?

A growing concern: Online access to minors’ health records

Hagström, Josefin

2025

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A proof-of-concept study for patient use of open notes with large language models

Salmi, Liz; Lewis, Dana M.; Clarke, Jennifer L.; Dong, Zhiyong et al.

Ingår i JAMIA Open, 2025

• DOI för A proof-of-concept study for patient use of open notes with large language models
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Adolescent and parental proxy online record access: analysis of the empirical evidence based on four bioethical principles

Hagström, Josefin; Hägglund, Maria; Blease, Charlotte

Ingår i BMC Medical Ethics, 2025

• DOI för Adolescent and parental proxy online record access: analysis of the empirical evidence based on four bioethical principles
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Adult Proxy Online Record Access - Differences Across Four Countries

Hägglund, Maria; Scott Duncan, Therese; Hagström, Josefin; Kujala, Sari et al.

Ingår i Studies in Health Technology and Informatics, s. 216-220, 2025

• DOI för Adult Proxy Online Record Access - Differences Across Four Countries
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Beyond counting clicks: rethinking engagement in digital mental health

Cipriani, Andrea; Ward, Thomas; Lambe, Sinéad; Ostinelli, Edoardo G. et al.

Ingår i British Journal of Psychiatry, 2025

• DOI för Beyond counting clicks: rethinking engagement in digital mental health
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Cancer Patients' Sharing of Electronic Health Records with Informal Caregivers

Hägglund, Maria; Rexhepi, Hanife; Blease, Charlotte; Hagström, Josefin et al.

Ingår i Studies in Health Technology and Informatics, s. 1291-1295, 2025

• DOI för Cancer Patients' Sharing of Electronic Health Records with Informal Caregivers
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Changes in documentation after implementing open notes in mental health care: Pre-post mixed methods study

Meier-Diedrich, Eva; Blease, Charlotte; Heinze, Martin; Wördemann, Jonas et al.

Ingår i Journal of Medical Internet Research, 2025

• DOI för Changes in documentation after implementing open notes in mental health care: Pre-post mixed methods study
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