Victimization in Cyberspace: Is It How Long We Spend Online, What We Do Online, or What We Post Online?

2020 ◽  
Vol 45 (4) ◽  
pp. 430-451
Author(s):  
Fawn T. Ngo ◽  
Alex R. Piquero ◽  
Jennifer LaPrade ◽  
Bao Duong
Keyword(s):  
Routine Activities Theory ◽  
Future Research ◽  
Convenience Sample ◽  
Online Activity ◽  
Actual Length ◽  
Online Victimization ◽  
Home Address ◽  
Types Of Information ◽  
Post Online ◽  
Online Posting

Prior research on cybercrime victimization has generally emphasized the linkage between the frequency or actual length of time individuals spend online engaging in certain activities and the risk of being victimized in cyberspace but has paid much less attention to what persons actually share or post online that increases the risk of online victimization. To address this gap, we appeal to the integrated lifestyle–routine activities theory in order to examine the relationships between the length of time one spends online (online frequency), specific activities or tasks one engages in while online (online activity), specific types of information one shares online (online posting), and seven specific forms of cybercrime victimization using a convenience sample of students. Results showed that one online frequency variable (internet hours), six online activity variables (banking, reading news, shopping, planning travel, socializing, and communicating with stranger), and three online posting variables (phone number, home address, and other info) were significantly related to five of the seven forms of cybercrime victimization (computer virus, harassment by nonstranger unwanted porn, sex solicitation, and phishing). Implications for our findings and directions for future research are discussed.

scholarly journals Self-rated health among undocumented and newly regularized migrants in Geneva: a cross-sectional study

2021 ◽  
Vol 21 (1) ◽  
Author(s):  
Julien Fakhoury ◽  
Claudine Burton-Jeangros ◽  
Idris Guessous ◽  
Liala Consoli ◽  
Aline Duvoisin ◽  
...  
Keyword(s):  
Social Support ◽  
Social Networks ◽  
Cross Sectional Study ◽  
Future Research ◽  
Undocumented Migrants ◽  
Long Term Effects ◽  
Residence Permit ◽  
Cross Sectional ◽  
Convenience Sample ◽  
Self Rated Health

Abstract Background In Europe, knowledge about the social determinants of health among undocumented migrants is scarce. The canton of Geneva, Switzerland, implemented in 2017–2018 a pilot public policy aiming at regularizing undocumented migrants. We sought to test for associations between self-rated health, proven eligibility for residence status regularization and social and economic integration. Methods This paper reports data from the first wave of the Parchemins Study, a prospective study whose aim is to investigate the effect of residence status regularization on undocumented migrants’ living conditions and health. The convenience sample included undocumented migrants living in Geneva for at least 3 years. We categorized them into those who were in the process of receiving or had just been granted a residence permit (eligible or newly regularized) and those who had not applied or were ineligible for regularization (undocumented). We conducted multivariate regression analyses to determine factors associated with better self-rated health, i.e., with excellent/very good vs. good/fair/poor self-rated health. Among these factors, measures of integration, social support and economic resources were included. Results Of the 437 participants, 202 (46%) belonged to the eligible or newly regularized group. This group reported better health more frequently than the undocumented group (44.6% versus 28.9%, p-value < .001), but the association was no longer significant after adjustment for social support and economic factors (odds ratio (OR): 1.12; 95% confidence interval (CI): 0.67–1.87). Overall, better health was associated with larger social networks (OR: 1.66; 95% CI: 1.04–2.64). This association remained significant even after adjusting for health-related variables. Conclusion At the onset of the regularization program, access to regularization was not associated with better self-rated health. Policies aiming at favouring undocumented migrants’ inclusion and engagement in social networks may promote better health. Future research should investigate long-term effects of residence status regularization on self-rated health.

A Comparison Between Self-Reported and Investigator-Measured Cardiovascular Risk-Related Biometric Numbers

2021 ◽  
pp. 019394592110135
Author(s):  
Sohye Lee ◽  
Catherine Pantik ◽  
Sree Duggirala ◽  
Ruth Lindquist
Keyword(s):  
Cardiovascular Risk ◽  
Fasting Blood Glucose ◽  
Health Assessment ◽  
Density Lipoprotein ◽  
Educational Interventions ◽  
Personal Knowledge ◽  
Future Research ◽  
Cardiovascular Risks ◽  
Convenience Sample ◽  
Glucose Levels

The purpose of this study was to examine individuals’ knowledge of cardiovascular risk-related biometric numbers and to compare self-reported and investigator-measured numbers in a convenience sample of adults in the Midwest region. Sociodemographic data and personal knowledge of cardiovascular risk-related biometric numbers were assessed using self-reported questionnaires. Investigators conducted health assessments to obtain biometric numbers. Among the 224 participants, participants’ reported knowledge about their cardiovascular risk-related biometric numbers was low, especially for high-density lipoprotein and fasting blood glucose levels. Participants’ knowledge was associated with education level and the recency of their last healthcare visit for health assessment. We found statistically significant mean differences between self-reported and investigator-measured blood pressure, and weight. This study found that there were discrepancies between self-reported and investigator-measured cardiovascular risk-related numbers. Future research is needed to develop educational interventions to improve personal knowledge of cardiovascular risks.

scholarly journals Evaluation of a short version of the Experiences in Close Relationships-Revised questionnaire (ECR-RD8): results from a representative German sample

2021 ◽  
Vol 9 (1) ◽  
Author(s):  
Johannes C. Ehrenthal ◽  
Johannes Zimmermann ◽  
Katja Brenk-Franz ◽  
Ulrike Dinger ◽  
Henning Schauenburg ◽  
...  
Keyword(s):  
Close Relationships ◽  
Full Scale ◽  
Self Report ◽  
Future Research ◽  
Short Version ◽  
German Population ◽  
Attachment Insecurity ◽  
Convenience Sample ◽  
Norm Values ◽  
Experiences In Close Relationships

Abstract Background Attachment insecurity is a prominent risk factor for the development and course of psychiatric and psychosomatic disorders. The Experiences in Close Relationships - Revised (ECR-R) questionnaire is a widely used self-report to assess attachment related anxiety and avoidance. However, its length has the potential to restrict its use in large, multi-instrument studies. The aim of this study was to develop and evaluate a brief version of the ECR-R, and provide norm values for the German population. Methods A screening version of the original ECR-R was developed through principal components analysis of datasets from several previous studies. In a representative sample of 2428 randomly selected individuals from the German population, we compared fit indices of different models by means of confirmatory factor analyses (CFA). We investigated the convergent validity of the screening version in an independent convenience sample of 557 participants. Correlations between the short and the full scale were investigated in a re-analysis of the original German ECR-R evaluation sample. Results CFA indicated a satisfactory model fit for an eight-item version (ECR-RD8). The ECR-RD8 demonstrated adequate reliability. The subscales correlated as expected with another self-report measure of attachment in an independent sample. Individuals with higher levels of attachment anxiety, but especially higher levels of attachment avoidance were significantly more likely to not be in a relationship, across all age groups. Correlations between the short and the full scale were high. Conclusions The ECR-RD8 appears to be a reliable, valid, and economic questionnaire for assessing attachment insecurity. In addition, the reported population-based norm values will help to contextualize future research findings.

scholarly journals Evaluation of African American Adolescent Health Status With Gender Comparison

2006 ◽  
Vol 4 (2) ◽  
pp. 168-174 ◽  
Author(s):  
Joy L. Anderson
Keyword(s):  
African American ◽  
Health Status ◽  
African American Adolescents ◽  
Healthy People ◽  
Health Concern ◽  
Future Research ◽  
Contributing Factors ◽  
Convenience Sample ◽  
African American Adolescent ◽  
Healthy People 2010

The goals of Healthy People 2010 are to increase the quality of life and life expectancy, and eliminate health disparities. There is no clear picture, however, if these goals are being addressed by African American adolescents. This study was conducted to evaluate health status of African American adolescents aged 13-19 in Florida’s Big Bend Region. Healthy People 2010 objectives were consulted for the evaluation. Responses from a convenience sample of 35 participants (63% female, 34% male) who completed a survey comprised of questions based on Likert scale are summarized here. The results show that the African American adolescents are engaging in some physical activity; however, only about half of them reported maintaining a healthy body weight. The majority of the adolescents reported avoiding smoking, but fewer adolescents reported avoiding drinking alcohol. Only a small percentage of the adolescents reported that their friends carried a gun or knife to school within the last 30 days; the percentage increased when the adolescents were asked if their friends got into a fist fight within the last 30 days. The adolescents sampled in this study have only achieved the Healthy People 2010 objectives in one of the health concern areas examined herein. It is also important to note that there are substantial gender-based disparities. In order to meet all Healthy People 2010 objectives, health education and promotion must be increased. Future research should explore different aspects of health status of adolescents in general, and further examine gender disparities and contributing factors.

scholarly journals Demographic and clinical characteristics of individuals’ Intentions to attend cardiac rehabilitation following hospitalization for heart failure: a descriptive analysis

2021 ◽  
Author(s):  
Kristen Cunningham
Keyword(s):  
Heart Failure ◽  
Pilot Study ◽  
Cardiac Rehabilitation ◽  
Clinical Characteristics ◽  
Descriptive Analysis ◽  
Future Research ◽  
Post Discharge ◽  
Convenience Sample ◽  
Rehabilitation Centers ◽  
Quantitative Descriptive

There is limited literature available that addresses heart failure patient attendance at cardiac rehabilitation centers. This quantitative descriptive pilot study used a convenience sample (n=30) to determine differences in socio-demographic and clinical characteristics and complications among individuals with heart failure who intended or did not intend to attend cardiac rehabilitation six weeks post-discharge. Findings suggest those intending to attend were significantly (p<0.05) older, unemployed/retired, received an income >$50,000, were able to drive, had lower functional classification scores, and experienced fewer complications over six weeks post-discharge. This descriptive pilot study provides an understanding of factors associated with intention to attend cardiac rehabilitation as well as the feasibility of the study design and procedures. Implications focus on strategies to increase potential attendance at cardiac rehabilitation in the heart failure population at the health care provider, organizational and policy levels as well as areas for future research.

“Tell Me More and Help Me to Decide, Doctor” – Information Seeking Attitudes and Use of Information Resources in Patients with Depression

2017 ◽  
Vol 41 (S1) ◽  
pp. S146-S146
Author(s):  
H. Almeida ◽  
A.M. Pisco Almeida ◽  
M. Figueiredo-Braga
Keyword(s):  
Decision Making ◽  
Information Seeking ◽  
Psychiatric Treatment ◽  
A Priori ◽  
Information Resources ◽  
Self Report ◽  
Mental Condition ◽  
Future Research ◽  
Limited Information ◽  
Convenience Sample

IntroductionShared decision-making (SDM) has shown to improve adherence, decrease hospitalization, and enhance knowledge of the illness and satisfaction with mental health services. Eliciting each patient's preferences for information allows tailoring the physician behavior according perspectives and expectations. Patients with depression (PWD) have frequently limited information regarding the availability and efficacy of psychiatric treatments.Aims/objectivesUnveil information seeking attitudes of patients with depression and their a priori use of digital sources of information.MethodsA convenience sample of PWD was submitted to a battery of self-report questionnaires. Standardized instruments were used to measure information seeking attitudes and the accessibility and usage of digital information resources.ResultsThirty-six patients were inquired, with a mean age of 39.8 (13.4) years. Information-seeking preferences were high, with an API-I score of 90.1 (13.8). Preferences for information-seeking behaviors were higher in severely depressed (P = 0.010) and less educated (P = 0.026) patients. Preferences were negatively correlated with length of psychiatric treatment (r = −0.514; P = 0.002). Sixty-one percent had a priori information regarding their psychiatric problem, and 68.8% considered it was influential in the decision-making behavior. Access and use of digital resources were correlated with education level (0.644; P = 0.000 and 0.554; P = 0.003), age (−0.357; P = 0.001 and −0.559; P = 0.007) and illness severity (−0.431; P = 0.04).ConclusionPatients with depression want to be informed about their mental condition and treatment options. Few resources are used and decision mostly relies on health professional's opinion and guidance. Accessible resources seem scarce and future research shall address the acceptance and impact of decisional-aid instruments on this population.

scholarly journals Translation and Validation of the Patient Activation Measure in Portuguese People with Type 2 Diabetes Mellitus

2018 ◽  
Vol 31 (7-8) ◽  
pp. 382 ◽  
Author(s):  
Liliana Laranjo ◽  
Vera Dias ◽  
Carla Nunes ◽  
Dagmara Paiva ◽  
Bill Mahoney
Keyword(s):  
Diabetes Mellitus ◽  
Type 2 Diabetes ◽  
Psychometric Properties ◽  
Rating Scale ◽  
Patient Activation ◽  
Future Research ◽  
Convenience Sample ◽  
European Portuguese ◽  
Patient Activation Measure

Introduction: Management of diabetes mellitus is largely dependent on patients’ active participation in care. The ‘Patient Activation Measure 13’ assesses patients’ knowledge, skills, and confidence in self-care. We aimed to translate, culturally adapt, and validate the ‘Patient Activation Measure 13’ to Portuguese, in people with type 2 diabetes.Material and Methods: The translation and cultural adaptation occurred in six phases. A convenience sample of people with type 2 diabetes was recruited from the waiting rooms of a diabetes outpatient centre in Lisbon, between March and April 2014. The questionnaire was self-administered; medical records were reviewed to obtain glycated haemoglobin levels. Main statistical analyses were based on the Rasch rating scale model.Results: The response rate for the final questionnaire was 76%. Rasch analysis was conducted on 193 respondents. Respondents had a mean age of 67.1 (SD 10.1) years, 42.7% were women, and the mean patient activation measure score (0 - 100) in the sample was 58.5 (SD 10.1). The sample was low to moderate in terms of activation: 40.4% were low in activation (levels 1 and 2), 49.7% were in level 3, and 9.8% were in level 4, the highest level of activation. All items had good fit and the response categories functioned well. Item reliability was 0.97 and person reliability was between 0.77 (real) and 0.83 (model). Discussion: The ‘Patient Activation Measure 13’ was translated and culturally adapted to European Portuguese and validated in people with diabetes, showing good psychometric properties. Future research should aim at evaluating test-retest reliability of the Portuguese ‘Patient Activation Measure 13’, and exploring its ability to measure changes in activation over time.Conclusion: The ‘Patient Activation Measure 13’ is now available in European Portuguese and has good psychometric properties. 

The effectiveness, feasibility and acceptability of a school-based intervention to improve sleep and psychological wellbeing in adolescents.

2021 ◽  
Author(s):  
Stephanie McCrory ◽  
Astrid McLellan ◽  
Karolina Kiper ◽  
Clare Munro ◽  
Christopher-James Harvey ◽  
...  
Keyword(s):  
Behavioural Therapy ◽  
Self Report ◽  
Psychological Wellbeing ◽  
Future Research ◽  
Convenience Sample ◽  
School Based ◽  
Cognitive Behavioural ◽  
Physical Health Problems ◽  
Improvement Interventions ◽  
Measure Change

Introduction: Adolescents are vulnerable to experiencing insufficient sleep which can increase the risk of developing insomnia, mental/physical health problems and mood regulation. School-based sleep improvement interventions (SBSII) have been developed utilising Cognitive Behavioural Therapy for Insomnia techniques and found improvements in sleep knowledge and behaviour. This study aimed to evaluate the effectiveness, feasibility and acceptability of a school-based sleep improvement intervention (iSLEEP) for improving sleep and psychological wellbeing in adolescents.Methods: A mixed-methods approach was adopted. The participants (115, aged 12-15) were recruited from secondary schools in Scotland. iSLEEP comprised of three lessons, combining formal sleep education and CBT-I, and were delivered over three consecutive weeks. Baseline (1 week before lesson 1) and follow-up (1 week following lesson 3) assessments comprised of self-report questionnaires to measure change in sleep, depression, anxiety and stress. Two weeks following the final lesson, a convenience sample of 19 pupils (14 females) were recruited to participate in focus groups.Results: There were significant improvements in overall sleep and marginal differences between those who were categorised with ‘probable insomnia’ at baseline and likewise for ‘good sleepers’. There were no significant improvements in symptoms of depression, anxiety or stress. Two themes and two sub-themes were generated. Participants reported that iSLEEP was acceptable and improved their sleep.Conclusions: These findings indicate that iSLEEP is an effective, feasible and acceptable SBSII. Future research should aim to utilise a controlled design to further investigate the efficacy of iSLEEP.

A Cross-Cultural Examination of Student Attitudes and Gender Differences in Facebook Profile Content

2013 ◽  
pp. 217-234
Author(s):  
Katherine Karl ◽  
Joy Peluchette ◽  
Christopher Schlagel
Keyword(s):  
Gender Differences ◽  
Student Attitudes ◽  
Cross Cultural ◽  
Future Research ◽  
Country Differences ◽  
And Gender ◽  
Types Of Information ◽  
Student Reports

This paper examines cultural and gender differences in student reports of the likelihood that they would post various types of information on their Facebook profiles and their attitudes regarding non-students accessing their profiles. Significant gender and country differences were found. In general, U.S. students were more likely than German students to report they would post extreme information. Males in both countries (U.S. and Germany) were more likely than females to self-promote and be extreme in the information they would post and less concerned if employers viewed their profiles. Both U.S. and German students reported several items they would likely post on their profiles, but did not want employers to see. Implications of these results and recommendations for future research are also discussed.

It's Not My Fault

2019 ◽  
Vol 30 (3) ◽  
pp. 18-37
Author(s):  
Tawei Wang ◽  
Yen-Yao Wang ◽  
Ju-Chun Yen
Keyword(s):  
Information Security ◽  
Information Transfer ◽  
Large Data ◽  
Future Research ◽  
Data Set ◽  
Security Breach ◽  
Security Breaches ◽  
Personally Identifiable Information ◽  
Types Of Information ◽  
Transfer Of Information

This article investigates the transfer of information security breach information between breached firms and their peers. Using a large data set of information security incidents from 2003 to 2013, the results suggest that 1) the effect of information security breach information transfer exists between breached firms and non-breached firms that offer similar products and 2) the effect of information transfer is weaker when the information security breach is due to internal faults or is related to the loss of personally identifiable information. Additional tests demonstrate that the effect of information transfer exhibits consistent patterns across time and with different types of information security breaches. Finally, the effect does not depend on whether the firms are IT intensive. Implications, limitations, and future research are discussed.

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