Background: The aim of this study was to determine if patient narratives and interviewer reactions are specific in groups of somatic (SF) and psychogenic fatigue (PF) patients.
Methods: The interview criteria and criteria of the interviewer reaction are tested against group classification. Over a 2-year period, 51 (22 PF and 29 SF) patients fulfilling the inclusion criteria were interviewed by two trained independent interviewers. The tape-recorded interviews were analyzed and blind rated by a set of independent physicians. State and Trait Anxiety Inventories (STAI and TRAI, respectively), Beck Depression Inventory (BDI), and Beck's hopelessness scales were completed by the patients.
Results: SF versus PF patients more often showed a clear versus vague qualitative description (P=.03), clear changes in levels of intensity (P=.03), and clear factors contributing to the increase (P=.02) and decrease (P=.03) of fatigue. In SF, the raters more often felt calm (P=.03), interested (P=.01), and attentive (P=.02). With PF tapes, the raters more often felt impatient (P=.03), surprised (P=.03), and helpless (P=.01). For the TRAI, the mean score of the PF group was significantly higher compared with that of the SF group (P=.004). For all items, Fisher's Exact Test was used.
Conclusions: Our results confirm significant differences in patient narratives and interviewer reactions for the groups examined. The systematic use of interview criteria and analysis of the interviewer reactions may contribute to the better understanding of fatigue.
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http://dx.doi.org/10.1016/j.jpsychores.2004.08.008 | DOI Listing |
BMC Pediatr
January 2025
Research Center for Caries Prevention, Dentistry Research Institute, Tehran University of Medical Sciences, Tehran, Iran.
Background: Parents of children born with cleft lip/palate encounter numerous challenges. This study aims to provide a deeper understanding for authorities to better support these parents by exploring the views and experiences of Iranian parents raising babies with cleft lip/palate through qualitative research.
Methods: This qualitative study collected data through face-to-face, in-depth, semi-structured interviews.
JMIR Res Protoc
January 2025
Quality Use of Medicines and Pharmacy Research Centre, UniSA Clinical and Health Sciences, University of South Australia, Adelaide, Australia.
Background: Adverse medicine events (AMEs) are unintended effects that occur following administration of medicines. Up to 70% of AMEs are not reported to, and hence remain undetected by, health care professionals and only 6% of AMEs are reported to regulators. Increased reporting by consumers, health care professionals, and pharmaceutical companies to medicine regulatory authorities is needed to increase the safety of medicines.
View Article and Find Full Text PDFJ Patient Rep Outcomes
January 2025
Institute of Rheumatology, Belgrade, Serbia.
Objectives: To translate, cross-culturally adapt and validate the Serbian Ankylosing Spondylitis Quality of Life (ASQoL) questionnaire, e.g. according to the new nomenclature Radiographic-Axial Spondyloarthritis (r-axSpA), and to relate it to disease activity and functional status domains.
View Article and Find Full Text PDFBr J Soc Psychol
January 2025
Institute of Psychology, University of Lausanne, Lausanne, Switzerland.
Degrowth-oriented climate change mitigation policies offer inspiring possibilities for future societies. However, they require radical change to individual and collective behaviours; and research has not yet fully addressed how people may anticipate future loss and threat when confronted with such policies. This study proposes a twofold examination of anticipated reactions to pro-environmental degrowth-oriented minority influence.
View Article and Find Full Text PDFBMC Prim Care
January 2025
Département des sciences de la santé, Université du Québec en Abitibi-Témiscamingue (UQAT), Rouyn-Noranda, Québec, Canada.
Background: The risks associated with medications and co-medications for chronic pain (CP) can influence a physician's choice of drugs and dosages, as well as a patient's adherence to the medication. High-quality care requires patients to participate in medication decisions. This study aimed to compare perceived risks of medications and co-medications between physicians and persons living with CP.
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