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Psychosocial Burden in People with Atopic Dermatitis: Effects of a Substance-Free Basic Skincare in a Randomized Health Care Study

C.C. Braren-von Stülpnagel, M. Augustin, R. Sommer & L. Westphal

The aims of this study were to compare clinical and psychosocial parameters between patients with a different severity of atopic dermatitis and to analyse the effect of an omega-6-fatty-acid-skin therapy.

DEVISE – Entwicklung und Evaluation einer Online-Intervention zur Reduktion von Selbststigmatisierung bei Menschen mit sichtbaren chronischen Hauterkrankungen

J. Traxler, C.F.Z. Stuhlmann, N. da Silva-Burger, C. Stierle, M. Rudnik & R. Sommer

Oral presentation presented at the 23rd DKVF Conference, Potsdam, Germany

Reducing self-stigma in chronic skin disease - Development and pilot-test of the HautKompass online programme

J. Traxler, C.F.Z. Stuhlmann, N. da Silva-Burger, C. Stierle, M. Rudnik & R. Sommer

Oral presentation presented at the European Health Psychology Society Conference (EHPS), Cascais, Portugal

Breaking Barriers: Randomized Controlled Trials Assessing an Intervention to Combat Stigma in Chronic Skin Disease

J. Traxler, C.C. Braren-von Stülpnagel, M. Augustin, M. Grosser & R. Sommer

Oral presentation presented at the 10th Appearance Matters Conference, Bristol, UK

Disease burden, patient needs and family planning in women of childbearing age with moderate to severe psoriasis

N. da Silva-Burger, B. Stephan, N. Ganjuur, M. Augustin & R. Sommer

Poster presented at the 33rd EADV Congress, Amsterdam, the Netherlands

Identifying Predictors and Correlates of Skin Disease Self-Stigma for Online RCT Intervention: A systematic review

CFZ. Stuhlmann, J. Traxler, V. Paucke, R. Sommer

Poster presented at the 52. Jahrestagung der Deutschen Dermatologischen Gesellschaft (DDG-Tagung), Berlin, Germany.

Tackling self-stigmatisation in people with visible chronic skin diseases - a systematic review and development of an online intervention

J. Traxler, C.F.Z. Stuhlmann, L. Westphal, H. Graf & R. Sommer

Oral presentation presented at the 25th World Congress of Dermatology, Singapore

Disease burden and patient needs in women of childbearing age with psoriasis: a comparative study with same-age men and older women using data from the German PsoBest registries

R. Sommer & N. da Silva

Oral presentation presented at the 25th World Congress of Dermatology, Singapore

Patient-reported Well-being in Value-based Care Using Tildrakizumab in a Real-world Setting: Protocol of a Multinational, Phase IV, 1-cohort Prospective Observational Study (the POSITIVE Study)

M. Augustin, R. Sommer, E. Daudén, P. Laws, E. de Jong, G. Fabbrocini, L. Naldi, A. Navarini, J. Lambert, Z. Reguiai, S. Gerdes, E. Massana, T. Obis, I. Kasujee, U. Mrowietz

Psoriasis is a chronic inflammatory skin disease that negatively impacts the quality of life of patients and their families. However, the most commonly used decision-making tools in psoriasis, Psoriasis Area and Severity Index (PASI), Physician Global Assessment (PGA) and Dermatology Life Quality Index (DLQI), do not fully capture the impact of psoriasis on patients' lives. In contrast, the well-established 5-item WHO Well-being Index (WHO-5) assesses the subjective psychological well-being of patients. Moreover, while drug innovations became available for psoriasis, data on the impact of these therapies on patients' lives and their closest environment (family, physicians) are limited. This study will assess the effect of tildrakizumab, an interleukin-23p19 inhibitor, on the overall well-being of patients with moderate-to-severe psoriasis. Moreover, the long-term benefit of tildrakizumab on physicians' satisfaction and partners' lives of patients with psoriasis will be evaluated.

Phase 1 of DEVISE Intervention: a Systematic Review Identifying Predictors and Correlates Associated with Self-stigma in People with Visible Chronic Skin Diseases

C.F.Z. Stuhlmann, J. Traxler, V. Paucke & R. Sommer

Oral presentation presented at the 25th World Congress of Dermatology, Singapore