Search

Introduction. Sexual behavior attitudes is a mix of constructs still addressed with inconsistent classifications by actual research, showing diverse theoretical structures. For that reason, we aimed to review the literature in the search for common patterns to bring in an exhaustive disambiguated proposal. Methods. We carried out a systematic review of sexual attitudes questionnaires and reviews. After that, following thematic analysis principles, we reviewed and categorized codes. Results. Of the 1126 screened publications, 89 scales and 62 reviews were assessed for eligibility. Of these, 28 were eventually included (15 questionnaires and 13 reviews). We classified 144 pieces of valid information into 17 groups based on content. Discussion. We conclude our work as a classification of broadly referenced self-oriented cognitive schemata of sexual behavior (SO-CSSB) as a first stage in the process of developing common classifications to overcome the inconsistency in the evaluation of sexual attitudes. [ABSTRACT FROM AUTHOR]

Purpose: Patients with multiple sclerosis (MS) are increasingly demanding access to reliable information regarding their disease. The objective of the INFOSEEK-MS study was to assess what are the strategies people with MS use when searching for information on their disease, including sources, frequency, reliability, and preferred content. Patients and Methods: A non-interventional, cross-sectional study was conducted. Patients with a diagnosis of MS according to the 2010 McDonald criteria were included. The InfoSeek questionnaire was used to assess patients' strategies when seeking information about the disease. Clinical characteristics and other variables, including disability, quality of life, fatigue, cognition, anxiety and depression, were analysed using the Expanded Disability Status Scale (EDSS), Multiple Sclerosis Impact Scale (MSIS-29), 5-item Modified Fatigue Scale (MFIS-5), Symbol Digit Modalities Test (SDMT), and Hospital Anxiety and Depression Scale (HADS), respectively. Results: Three hundred and two patients were studied (mean age: 42.3 ± 10 years, 64% female, mean disease duration: 9.6 ± 7.0 years, 90% with relapsing-remitting MS, and mean EDSS score: 2.6 ± 1.9). The internet (either via mobile or computer) is a frequently reported source of information. Lifestyle-related information (67.2%), research and emerging treatments (63.6%), symptom control (49.7%), sharing experiences with other patients (46.4%), and disease prognosis (46.4%) were the most searched topics. Neurologists and nurses were the most trusted source of information. Younger patients and higher SDMT scores were associated with all search resources (M = 37.7 and M = 49.97, respectively). The frequency of searches was related to the number of relapses (R2 = 0.07), EDSS (R2 = 0.14), MSIS-29 physical and psychological components (R2 = 0.132) and inversely with depression (R2 = 0.132). Conclusion: Although healthcare professionals are considered the most reliable source of information for people with MS, searching for information on the Internet is very frequent. An individualized information strategy considering the different factors involved is needed. [ABSTRACT FROM AUTHOR]