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Gefahrenlagen, wie schwere Unwetter, Terroranschläge oder die COVID-19-Pandemie, stellen aktuell und zukünftig eine Bedrohung unserer Gesellschaft dar. Im Fall dieser und weiterer Gefahren können Warnungen helfen, Schäden zu verhindern und Menschenleben zu retten, indem sie die Empfänger*innen informieren und Schutzmaßnahmen vermitteln. Das Protective Action Decision Model (PADM) (Lindell & Perry, 2012) bietet einen theoretischen Rahmen, der Verarbeitungsprozesse von Warnungen und die Entstehung von Schutzverhalten abbildet. Neben zahlreichen weiteren Elementen beinhaltet das PADM die Wahrnehmung von Risiko als zentralen Faktor. Im Sinne des Modells sowie bereits existierender Literatur wird Risikowahrnehmung jedoch häufig ausschließlich kognitiv abgebildet. Zudem untersuchen Studien vorwiegend einzelne Gefahrenlagentypen oder singuläre Ereignisse.
Die vorliegende Arbeit bildet mit drei Beobachtungsstudien sowie einer experimentellen Studie Verarbeitungsprozesse von Warnungen vor verschiedenen Gefahrenlagen ab. Untersucht wurde der Einfluss der Warnungen auf kognitive und affektive Facetten der Risikowahrnehmung und ihre Rolle bei der Suche nach Informationen sowie der Intention, Schutzverhalten auszuführen. Über Online-Befragungen erhielten die Teilnehmenden Warnungen zu verschiedenen Gefahrenlagen (schweres Unwetter, Großbrand, extreme Gewalttat, Ausfall der Notrufnummer, Fund einer Weltkriegsbombe, COVID-19-Pandemie, Gewitter), die Informationen zur Gefahr sowie Handlungsempfehlungen enthielten. Befragt wurden sie unter anderem hinsichtlich ihrer Risikowahrnehmung vor und nach Warnerhalt sowie ihrer Intention, die angegebenen Schutzmaßnahmen zu befolgen oder sich Informationen zu suchen. Zudem wurden Eigenschaften der Warnungsempfänger*innen erhoben.
Die Ergebnisse stärken die Rolle affektiver Risikowahrnehmung für die Verarbeitung
von Warnungen sowie die Entstehung von Schutzverhalten und Informationssuche. Dies gilt
jedoch nicht für alle Gefahrenlagen gleichermaßen, sodass der Einfluss von Eigenschaften der Gefahr, wie Häufigkeit oder Schweregrad, deutlich wird. Bezüglich der Eigenschaften der Empfänger*innen ergab sich ebenfalls kein einheitliches Bild. Basierend auf den Ergebnissen wird eine Erweiterung des PADM um ein Modellelement der affektiven Risikowahrnehmung vorgeschlagen.
Fortführende Forschung zu Warnungen sollte eine multifacettierte Sichtweise von Risikowahrnehmung anstreben. Darüber hinaus sollten Gefahrenlagen vergleichend untersucht und ihre Eigenschaften sowie Eigenschaften der Warnungen systematisch variiert werden.
Introduction: To maintain a sufficient donor pool, deferred first-time donors (FTD) should be motivated to return for blood donation. This pilot study investigates how deferral affects momentary mood, satisfaction with the donation process, and subsequent return behavior to examine their potential for motivating (deferred) FTD. Methods: All of the subjects (n = 96) completed a first questionnaire (A1) before pre-donation assessment. Deferred FTD (n = 22) were asked to complete a second questionnaire (A2) immediately after deferral, while non-deferred FTD (n = 74) filled in the second questionnaire (A3) after blood donation. The impact of deferral, momentary mood, and satisfaction with the donation process on return behavior within 12 months was tested by calculating two path analyses, controlling for sex and age. Results: Mood (p < 0.001) and satisfaction with social aspects of the donation process (p = 0.01) were decreased after deferral. Deferred FTD were less likely than non-deferred FTD to return to the blood donation center within 12 months (60.8 vs. 36.4%; p = 0.043). However, path analyses revealed that deferral effects on mood and satisfaction were not connected to return behavior. Instead, age had a significant influence on return behavior (p < 0.05) such that, overall, non-returning FTD were older than returning FTD, regardless of their deferral status. Conclusion: Our findings suggest that mood and satisfaction with the donation process are directly affected by deferral but not clearly responsible for low return rates. It seems promising to embed these variables in established health behavior models in further studies to increase the return rates of deferred FTD.
Abstract
Background
The need to optimize exposure treatments for anxiety disorders may be addressed by temporally intensified exposure sessions. Effects on symptom reduction and public health benefits should be examined across different anxiety disorders with comorbid conditions.
Methods
This multicenter randomized controlled trial compared two variants of prediction error‐based exposure therapy (PeEx) in various anxiety disorders (both 12 sessions + 2 booster sessions, 100 min/session): temporally intensified exposure (PeEx‐I) with exposure sessions condensed to 2 weeks (n = 358) and standard nonintensified exposure (PeEx‐S) with weekly exposure sessions (n = 368). Primary outcomes were anxiety symptoms (pre, post, and 6‐months follow‐up). Secondary outcomes were global severity (across sessions), quality of life, disability days, and comorbid depression.
Results
Both treatments resulted in substantial improvements at post (PeEx‐I: dwithin = 1.50, PeEx‐S: dwithin = 1.78) and follow‐up (PeEx‐I: dwithin = 2.34; PeEx‐S: dwithin = 2.03). Both groups showed formally equivalent symptom reduction at post and follow‐up. However, time until response during treatment was 32% shorter in PeEx‐I (median = 68 days) than PeEx‐S (108 days; TRPeEx‐I = 0.68). Interestingly, drop‐out rates were lower during intensified exposure. PeEx‐I was also superior in reducing disability days and improving quality of life at follow‐up without increasing relapse.
Conclusions
Both treatment variants focusing on the transdiagnostic exposure‐based violation of threat beliefs were effective in reducing symptom severity and disability in severe anxiety disorders. Temporally intensified exposure resulted in faster treatment response with substantial public health benefits and lower drop‐out during the exposure phase, without higher relapse. Clinicians can expect better or at least comparable outcomes when delivering exposure in a temporally intensified manner.
Abstract
Lately, the use of patient‐reported outcome measures (PROM) to adapt and improve ongoing psychotherapeutic treatments has become more widespread. Their main purpose is to support data‐informed, collaborative treatment decisions which include the patient's point of view on their progress. In case of nonresponse or deterioration, these systems are able to warn clinicians and guide the process “back on track” in treatment. In this case illustration, the Greifswald Psychotherapy Navigator System (GPNS) detected the deterioration of 19‐year‐old Sarah during the first eight sessions of cognitive‐behavioral therapy for social anxiety and depression. Here, the GPNS helped the therapist gain insight as to how Sarah's social anxiety affected their treatment and adjust her strategy accordingly. Using the symptom curves and progress scales of the GPNS, the therapist was able to then address her patient's struggles in detail during their sessions and with her supervisor. After adapting her therapeutic approach, the patient's deterioration could be averted while simultaneously strengthening their communication in the process. Clinical implications and the benefits of using PROM systems for evidence‐based personalization of psychotherapy are presented.
Body dissatisfaction is pervasive among young women in Western countries. Among the many forces that contribute to body dissatisfaction, the overrepresentation of thin bodies in visual media has received notable attention. In this study, we proposed that prevalence-induced concept change may be one of the cognitive mechanisms that explain how beauty standards shift. We conducted a preregistered online experiment with young women (N = 419) and found that when the prevalence of thin bodies in the environment increased, the concept of being overweight expanded to include bodies that would otherwise be judged as “normal.” Exploratory analyses revealed significant individual differences in sensitivity to this effect, in terms of women’s judgments about other bodies as well as their own. These results suggest that women’s judgments about other women’s bodies are biased by an overrepresentation of thinness and lend initial support to policies designed to increase size-inclusive representation in the media.
Abstract. Most feedback we receive or give is correct (deterministic
feedback), though a small fraction can be wrong for various reasons. Children need to cope
with receiving some portion of wrong feedback (stochastic feedback). It is still unknown
if better social functioning and communication skills or outstanding intelligence (IQ) or
chronological age support children in the coping process. We tested a sample of
7-, 9-, and 11-year-old children (N = 60) who deduced a
sequence of four left and right button presses from a red and green stochastic feedback
signal that was wrong in 15 % of the trials. Children performed worse with
stochastic than with deterministic feedback but improved in the repeated trials,
especially after receiving positive feedback about whether true or false. Controlling for
IQ improved and confirmed these effects, while social and communicative competence
explained little or no variance.
Zusammenfassung. Die Vereinbarkeit von Wissenschaft und Familie ist für Eltern im
Allgemeinen und Frauen im Besonderen eine große Herausforderung. Tagungsteilnahmen sind wichtige
Karrierebausteine und eine organisatorische Herausforderung für Eltern. In diesem Positionspapier wird
ein Stimmungsbild zu familienfreundlicheren Kongressgestaltung in der Fachgruppe (FG) Klinische Psychologie
und Psychotherapie der Deutschen Gesellschaft für Psychologie (DGPs) erfragt. 147 FG-Mitglieder
(Rücklaufquote: 18.36 %) beantworteten Fragen zur Demographie, sowie Einstellungen gegenüber
der FG-Tagung, Betreuungsmöglichkeiten und familienfreundlichen Maßnahmen. Von den Teilnehmenden
waren 66 % Eltern, 45 % sagten wegen familiärer Verpflichtungen die FG-Tagung ab.
Zusätzliche Kosten durch familiäre Verpflichtungen wurden als hoch eingeschätzt und
familienfreundlichere Maßnahmen von vielen Teilnehmenden gewünscht. Familienfreundliche Konferenzen
können ein klares Signal der Inklusion und Solidarität setzen und für die Aufrechterhaltung und
Nachhaltigkeit wissenschaftlicher Kompetenz sorgen. Konkrete Empfehlungen für eine familienfreundliche
Konferenzgestaltung werden als Checkliste im elektronischen Anhang zur Verfügung gestellt.
Background
Longitudinal observational studies play on an important role for evidence-based research on health services and psychiatric rehabilitation. However, information is missing about the reasons, why patients participate in such studies, and how they evaluate their participation experience.
Methods
Subsequently to their final assessment in a 2-year follow-up study on supported housing for persons with severe mental illness, n = 182 patients answered a short questionnaire on their study participation experience (prior experiences, participation reasons, burden due to study assessments, intention to participate in studies again). Basic respondent characteristics as well as symptom severity (SCL-K9) were also included in the descriptive and analytical statistics.
Results
To help other people and curiosity were cited as the main initial reasons for study participation (>85%). Further motives were significantly associated with demographic and/or clinical variables. For instance, “relieve from boredom” was more frequently reported by men and patients with substance use disorders (compared to mood disorders), and participants ‘motive” to talk about illness” was associated with higher symptom severity at study entry. Furthermore, only a small proportion of respondents indicated significant burdens by study participation and about 87% would also participate in future studies.
Conclusions
The respondents gave an overall positive evaluation regarding their participation experience in an observational study on psychiatric rehabilitation. The results additionally suggest that health and social care professionals should be responsive to the expectations and needs of patients with mental illness regarding participation in research.
Given the increasing prevalence of chronic kidney disease (CKD) and its impact on health care, it is important to better understand the multiple factors influencing health-related quality of life (HRQOL), particularly since they have been shown to affect CKD outcomes. Determinants of HRQOL as measured by the validated Kidney Disease Quality of Life questionnaire (KDQOL) and the Patient Health Questionnaire depression screener (PHQ-9) were assessed in a routine CKD patient sample, the Greifswald Approach to Individualized Medicine (GANI_MED) renal cohort (N = 160), including a wide range of self-reported data, sociodemographic and laboratory measures. Compared to the general population, CKD patients had lower HRQOL indices. Dialysis was associated with (1) low levels of physical functioning, (2) increased impairments by symptoms and problems, and (3) more effects and burden of kidney disease. HRQOL is seriously affected in CKD patients. However, impairments were found irrespective of eGFR decline and albuminuria. Rather, the comorbid conditions of depression and diabetes predicted a lower HRQOL (physical component score). Further studies should address whether recognizing and treating depression may not only improve HRQOL but also promote survival and lower hospitalization rates of CKD patients.
Loneliness and lack of belonging as paramount theme in identity descriptions of Children Born of War
(2022)
Objective
Children Born of War (CBOW) are an international and timeless phenomenon that exists in every country involved in war or armed conflict. Nevertheless, little is known on a systematic level about those children, who are typically fathered by a foreign or enemy soldier and born to a local mother. In particular, the identity issues that CBOW often report have remained largely uninvestigated. In the current qualitative study we began filling this gap in the scientific literature by asking how CBOW construct their identity in self-descriptions.
Method
We utilized thematic content analysis of N = 122 German CBOWs' answers to an open-ended questionnaire item asking how they see themselves and their identity in the context of being a CBOW.
Results
We identified five key themes in CBOW' identity accounts. Loneliness and lack of belonging appeared as a paramount aspect of their self-descriptions next to narratives about belonging and positive relationship. On a less interpersonal basis, we found fighting and surviving and searching for truth and completion overarching aspects of their identities. There were also few accounts growing up unaffected by the fact of being born a CBOW. Although all themes portray different perspectives, they all (but the last one) clearly indicate the impeded circumstances under which CBOW had to grow up.
Conclusions
Integrating our findings with existing interdisciplinary literature regarding identity, we discuss implications for future research and clinical and political practice.