Publikationen

2021

Schulze M, Breuning M, Holmberg C, Müller-Nordhorn J. The Evaluation of a Health Website Presenting Real User (Patients’) Experiences. 2021 (forthcoming).

Holmberg C, Breuning M. Personal Experience of Illness. In: Scrimshaw SC, Lane SD, Rubinstein RA, Fisher J, editors. Sage Handbook of Social Studies in Health and Medicine. 2021; p. 143-161.

Kaiser M, Adami S, Lucius-Hoene G, Muller-Nordhorn J, Goerling U, Breuning M, Holmberg C. Learning-by-doing: the importance of experiential knowledge sharing for meeting the information needs of people with colorectal cancer in Germany-a qualitative study. BMJ Open. 2021;11(2):e038460.

Blödt S, Müller-Nordhorn J, Seifert G, Holmberg C. Trust, medical expertise and humaneness: A qualitative study on people with cancer' satisfaction with medical care. Health Expect. 2021;24(2):317-26.

2020

Schultze M, Müller‐Nordhorn J, Holmberg C. Discussing the effects of prostate cancer beyond biographical disruption and new normalcy: the experiences of men with prostate cancer in Germany. Sociology of health & illness. 2020; 42(6), p.1359-78.

Holmberg C, Adami S. Leben mit dem Stoma. Der Onkologe. 2020; 26(12):1162.

Holmberg C. Krankheitsnarrative in der Versorgungsforschung. In: Netzwerk Qualitative Gesundheitsforschung, editor. Perspektiven qualitativer Gesundheitsforschung 2020; p. 99-115.

Breuning M, Schäfer-Fauth L, Lucius-Hoene G, Holmberg C. Connecting one’s own illness story to the illness experiences of others on a website - An evaluation study using the think aloud method. Patient Education and Counseling. 2020; 103(1), p. 199-207.

2018

Lucius-Hoene G, Holmberg C, Meyer T, editors. Illness Narratives in Practice: Potentials and Challenges of Using Narratives in Health-related Contexts. Oxford: Oxford University Press; 2018.

Lucius-Hoene G, Breuning M, Helfferich C. Illness narratives in practice: Which questions do we have to face when collecting and using them? In: Lucius-Hoene G, Holmberg C, Meyer T, editors. Illness Narratives in Practice: Potentials and Challenges of Using Narratives in Health-related Contexts. Oxford: Oxford University Press; 2018.

Palant A, Himmel W. How to use illness narratives in medical education: First teaching experiences with the German DIPEx website project. In: Lucius-Hoene G, Holmberg C, Meyer T, editors. Illness Narratives in Practice: Potentials and Challenges of Using Narratives in Health-related Contexts. Oxford: Oxford University Press; 2018; p. 152-63.

Blödt S, Kaiser M, Adam Y, Adami S, Schultze M, Müller-Nordhorn J, Holmberg C. Understanding the role of health information in patients’ experiences: secondary analysis of qualitative narrative interviews with people diagnosed with cancer in Germany. BMJ open. 2018; 8(3):e019576-e.

Adami S, Breuning M, Bengel J, Bischoff A, Peng-Keller S. Chronische Schmerzpatientinnen und -patienten sprechen über ihre Spiritualität. Spiritual Care. 2018; 7(3), p. 243-53.

2017

Giesler JM, Keller B, Repke T, Leonhart R, Weis J, Muckelbauer R,..., Holmberg C. Effect of a Website That Presents Patients' Experiences on Self-Efficacy and Patient Competence of Colorectal Cancer Patients: Web-Based Randomized Controlled Trial. Journal of medical Internet research. 2017; 19(10):e334-e.

Engler J, Güthlin C, Dahlhaus A, Kojima E, Müller‐Nordhorn J, Weißbach L, Holmberg C. Physician cooperation in outpatient cancer care. An amplified secondary analysis of qualitative interview data. European journal of cancer care. 2017; 26(6):e12675-n/a.

Breuning M, Lucius-Hoene G, Burbaum C, Himmel W, Bengel J. Subjektive Krankheitserfahrungen und Patientenorientierung: Das Website-Projekt DIPEx Germany. Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz. 2017; 60(4):453-61.

2016

Engler J, Adami S, Adam Y, Keller B, Repke T, Fügemann H,..., Holmberg C. Using others' experiences. Cancer patients' expectations and navigation of a website providing narratives on prostate, breast and colorectal cancer. Patient Educ Couns. 2016; 99(8), p. 1325-32.

Breuning M, Hettmer S, Strahm B, Bengel J, Niemeyer C. Krebskranke Kinder und ihre Familien: Verständnis für das Erleben. Deutsches Ärzteblatt. 2016;113(51), p. 2362-3.

2015

Lucius-Hoene G, Breuning M, Palant A. Patientenerfahrungen als Ressource: Die Website krankheitserfahrungen. de. In: Amelung VE, Eble S, Hildebrandt H, Kieps F, Längel R, Ozegowski S, et al., editors. Patientenorientierung Schlüssel für mehr Qualität (Schriftenreihe des Bundesverbandes Managed Care). Berlin: MWV Medizinisch Wissenschaftliche Verlagsgesellschaft; 2015; p. 248-53.

2013

Lucius-Hoene G, Groth S, Becker A-K, Dvorak F, Breuning M, Himmel W. Wie erleben Patienten die Veröffentlichung ihrer Krankheitserfahrungen im Internet? Die Rehabilitation. 2013; 52(3), p. 196-201.

2012

Lucius-Hoene G, Thiele U, Breuning M, Haug S. Doctors' voices in patients' narratives: coping with emotions in storytelling. Chronic illness. 2012;8(3), p.163-75.