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Spss statistics software version 21

Manufactured by IBM
Sourced in United States, Japan

SPSS Statistics software version 21 is a statistical analysis tool. It provides a comprehensive set of features for data management, analysis, and presentation. The software enables users to perform a wide range of statistical procedures, including descriptive analytics, predictive modeling, and advanced statistical techniques.

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222 protocols using spss statistics software version 21

1

Examining ADHD Symptom Impact on Functional Impairment

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We assessed differences between ADHD and control subjects using t tests for continuous variables and chi-square tests for categorical outcomes. Pearson correlation coefficients were used to evaluate relationships between clinical variables.
Mediation models were developed to examine the influence of ADHD symptom severity on functional impairment. Separate model were estimated for each independent variable (subscales from CAARS) and dependent variable (SDS scores). Mediation models estimate the indirect effects of an independent variable (in this case, ADHD symptom severity) on a dependent variable (functional impairment) after accounting for a mediator (anxiety). We used 5,000 bootstrap resamples to provide stable estimates of direct, indirect, and total effects. Confidence intervals were established using the bias-corrected and accelerated method. Mediation was tested using the Hayes40) PROCESS modeling approach in model 4 of IBM SPSS Statistics software version 21.0 (IBM Co., Armonk, NY, USA). This analytic approach permitted the examination of both direct and indirect effects of ADHD symptom severity and anxiety on functional impairment in subjects with adult ADHD.
All tests were two-tailed, and alpha level was set at 0.05 for all analyses. We calculated all statistics using IBM SPSS Statistics software version 21.0.
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2

Biomarkers for Predicting COVID-19 Severity

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Categorical variables were described as frequency rates and percentage, and continuous variables were described using mean±standard deviation (SD) and median (IQR). A normality test was performed using Kolmogorov–Smirnov test. Normally distributed data were analyzed using an independent t-test, while non-normally distributed data were analyzed using the Mann–Whitney U-test. Non-normally distributed data from repeated measures were also compared using the generalized linear mixed model. The area under the curve (AUC) and 95% confidence interval (CI) of the receiver operating characteristic (ROC) curve were used to assess the accuracy of each biomarker in predicting COVID-19 severity. The severity of COVID‐19 was predicted by optimal cut‐off points determined by Youden’s index. All data and statistical analysis were conducted using IBM SPSS Statistics software version 21.0 (IBM Corp., Armonk, NY, USA). Two-sided p-values <0.05 were considered to indicate statistically significant differences.
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3

Statistical Analysis of Research Variables

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The entire statistical analysis was performed using the IBM SPSS statistics software, version 21.0 (Chicago, IL, USA). The variables were compared using Fisher’s exact test with significance level of 5%. Values of P<0.05 were considered significant for the analysis.
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4

Statistical Analysis of Survival Outcomes

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Statistical analyses were performed using IBM SPSS statistics software, version 21.0 (IBM Corp., Armonk, NY, USA). The corresponding figures were drawn using GraphPad Prism v6.0 software (GraphPad Software Inc., La Jolla, CA, USA). Categorical variables are presented as percentages, and their comparisons were assessed using the Chi-square test or Fisher's exact test. Continuous variables are presented as the median (range). The Mann-Whiney U test was used for two-group comparisons, and the Kruskal-Wallis H test was used for multiple group comparisons. Survival outcomes were evaluated by the Kaplan-Meier method and compared using the log-rank test. Parameters for which P < 0.05 for OS in the univariate Cox models were further assessed in multivariate Cox models. Hazard ratios (HRs) and 95% confidence intervals (CIs) were subsequently generated. The statistical tests used above were two- sided, and a P value <0.05 was considered significant.
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5

Quantifying Ocular Microvascular Changes

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Descriptive and frequency statistics will be used to assess qualitative variables. Normality of quantitative variables (i.e. pixel area) will be examined using histograms and the Kolmogorov-Smirnov test protected by the Bonferroni correction. To assess differences in quantitative measurements between study groups, parametric and non-parametric tests will be performed as appropriate, respectively. Correlation between clinical data and OCTA derived measurements will be analyzed using a multivariate regression model to assess the effects of clinical characteristics on these values. Visual acuity measured in Snellen notation was converted to logMAR (logarithm of the minimum angle of resolution) equivalents for the purposes of statistical analysis. VA values recorded as counting fingers (CF), hand movements (HM), and perception of light (PL) were converted to 2.1, 2.4, and 2.7 LogMAR, respectively. A p value of less than 0.05 will be considered statistically significant. All statistical analysis will be performed using IBM SPSS Statistics software version 21.0 (IBM Corp., Armonk, NY, USA).
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6

Cephalometric Analysis of Dental and Skeletal Changes

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Statistical analyses were conducted using IBM SPSS Statistics software version 21.0 (IBM Co., Armonk, NY, USA); p-values less than 0.05 were considered statistically significant. Time-dependent changes in cephalometric measurement variables indicating dental and skeletal changes were compared with one-way analysis of variance (ANOVA) and Duncan's post-hoc test in each group. Independent sample t-tests were used to compare the differences between the groups.
The intraassessor reproducibility of the measurements was determined by evaluating the variables of 10 randomly selected patients twice, at 3-week intervals, according to the intraclass correlation coefficient (ICC). The mean ICC was 0.965 in the 95% confidence interval.
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7

Rasch Analysis of ICF Components

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SPSS Statistics software version 21.0 (IBM Corporation) was used to analyze the demographic and disease data. RUMM2030 software (RUMM Laboratory Pty) was used to perform the Rasch analysis. For each component of the ICF set, the overall fit to a Rasch model was examined. If the overall fit was not good, poorly fitting categories were identified and deleted. Another round of Rasch analysis was then run until adequate overall fit was attained. The following properties of the ICF set were examined.
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8

Clinical Predictors of Favorable Outcome

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Baseline clinical variables with statistically significant associations with favorable outcome and TAI were included in a multivariable logistic regression analysis. Association of baseline clinical variables with favorable outcome was evaluated using logistic regression. The assessment of the association of baseline clinical variables with the TAI measures was performed using one-way Kruskal–Wallis ANOVA for ordinal variables, Spearman’s correlation coefficient for non-parametrically distributed variables, fit of the regression R [2 ] for parametrically distributed variables, and the Wilcoxon signed-rank test for dichotomized data.
Statistical significance was set to a p value < 0.05 for all analyses. Analyses were performed using IBM SPSS Statistics software, version 21.0 (IBM Corporation, Armonk, NY, USA).
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9

Familial Risk and Correlation of Hepatocellular Carcinoma

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The Kaplan-Meier survival analysis was conducted to estimate the lifetime cumulative risk of HCC for the relatives of cases and controls as well as for case families stratified by type of relatives (first-degree relatives, second-degree relatives, no blood relatives). A log-rank test was used to test differences between the survival curves.
Cross ratio (CR) function [11] was used to assess the familial correlation of onset age for HCC. The null value for CR is 1 and a larger value indicates a stronger dependence of onset age for HCC between two members. CR was estimated using the approach of stratified Cox proportional hazard model [12] (link), [13] . Model parameters were estimated using the method of maximum partial likelihood. All models are stratified by age of the probands’ (<50 and ≥50 years). We accounted for the non-independence of observations within families by using a robust variance estimate [14] (link). All analyses were carried out using the IBM SPSS statistics software version 21.0.
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10

Fracture Complexity and Bone Health Factors

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Data analysis was performed using SPSS statistics software version 21.0 (IBM Corp, Armonk, NY). Patients were characterised by age, gender, mean T-scores, BMD (normal/osteopaenia/osteoporosis), mean CI and type of fracture (simple/complex). Continuous outcome variables were checked for a normal distribution. To study the differences in mean T-scores and CI between the simple and complex fracture groups, independent samples t-tests were used. This relationship was also studied by testing whether the frequencies of osteoporosis and osteopaenia were equally distributed among simple and complex fracture groups, using a chi-squared test. In addition, we tested whether there was a correlation between T-scores and CI using Pearson’s correlation coefficients.
Consequently, we studied the effect of gender, age and BMI on our primary outcome measures. The independent samples t-test was used to investigate differences in age between the simple and complex fracture group, and to examine differences in T-scores and CI between men and women.
Finally, we investigated the relationship between T-scores and fracture complexity, and between CI and fracture complexity, adjusted for age, gender and BMI, using a logistic regression analysis.
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