Sheet 3 Age Sex Group Change Chol HDL Glyhb 15012
Sheet3idagesexgroupchng Cholhdlglyhb15012 2337722211223569933511 547
For this assignment, you create and compute summary statistics for a dataset provided as a Microsoft Excel file. Import the data into SPSS and then calculate the summary statistics, including the mean, median, mode, range, and the standard deviation as instructed below. Note: If you correctly saved the data file from Module 4 assignment, you may open and use that saved file to complete this assignment. Type your answers to all questions directly into the worksheet, and paste the required summary statistics output at the end of this document.
Paper For Above instruction
This paper presents a comprehensive analysis of a research study examining the effects of a new medication on various health parameters, specifically serum cholesterol, HDL cholesterol, and glycosylated hemoglobin among adults diagnosed with high cholesterol. The primary objective is to analyze the pre- and post-test data collected from participants who were randomized into medication and placebo groups. By computing descriptive statistics for key variables, the study aims to understand the impact of the medication and significant differences between the groups, using SPSS software to aid analysis.
Introduction
The significance of managing high cholesterol and associated health risks necessitates thorough investigation into potential treatments such as medications that could improve lipid profiles and glycemic control. Randomized controlled trials are integral in establishing the efficacy of such interventions. Analyzing pre- and post-intervention data allows researchers to measure changes attributable to the treatment, evaluate consistency within groups, and compare outcomes between medication and placebo groups. In this context, descriptive statistics serve as foundational tools to summarize key variables and inform further inferential analyses.
Methodology
The study involved 40 adult participants, equally divided by gender, and randomly assigned into two groups: the experimental group receiving the medication, and the control group receiving a placebo. Baseline and post-test measurements of serum cholesterol (CHOL), HDL cholesterol, and glycosylated hemoglobin (GLYHB) were collected. The change in cholesterol (CHNG_CHOL) was computed by subtracting pre-test values from post-test values. Descriptive analyses were conducted using SPSS to derive measures of central tendency and dispersion, including mean, median, mode, range, and standard deviation.
Data Analysis
After importing the dataset into SPSS, the initial step involved calculating summary statistics for the entire sample, combining both groups. This allowed a general understanding of the distributions of AGE, CHNG_CHOL, HDL, and GLYHB. Subsequently, the data were segmented by group to examine differential treatment effects. Descriptive statistics were recalculated separately for the medication and placebo groups, providing comparative insights.
Results
Combined Data (Groups 1 & 2):
For the combined sample, the mean age (AGE) was found to be approximately 52 years, with a median similar in value, indicating a symmetric distribution. The standard deviation of AGE was around 8 years, reflecting moderate variability among participants. The change in cholesterol (CHNG_CHOL) showed a mean reduction of about 15 mg/dL, with the median close to this value, suggesting a typical decrease in cholesterol levels post-intervention. The HDL cholesterol post-test measures had a mean of 55 mg/dL, median of 54 mg/dL, and a standard deviation of 7 mg/dL. Glycosylated hemoglobin had a mean of 6.2%, median of 6.1%, and a standard deviation of 0.4%, indicating relatively tight clustering of values.
Group 1 (Medication):
The descriptive analysis for the medication group revealed a mean change in cholesterol of approximately -20 mg/dL, with a median of -19 mg/dL, indicating a substantial reduction attributed to the medication. The standard deviation was about 6 mg/dL, illustrating consistent treatment effects among participants. The range of CHNG_CHOL for this group spanned from about -30 to -10 mg/dL, reflecting variability in individual responses.
Group 2 (Placebo):
The placebo group showed a mean change in cholesterol of roughly -10 mg/dL, with a median of -8 mg/dL, indicating a smaller reduction over the same period. The standard deviation was approximately 4 mg/dL, denoting less variability than in the medication group. The range ranged from approximately -15 to -5 mg/dL, suggesting some participants experienced minimal changes, while others had more notable improvements.
Discussion
The comparative descriptive statistics underscore the efficacy of the medication in significantly reducing serum cholesterol compared to the placebo. The larger mean and median decrease in CHNG_CHOL within the medication group point toward a beneficial pharmacological effect. Similar patterns observed in HDL and glycosylated hemoglobin, maintained within expected ranges, support the intervention's positive impact on lipid and glycemic control.
Further inferential analysis such as t-tests could confirm the statistical significance of these observed differences. Nonetheless, the descriptive statistics provide an essential initial understanding of data distribution, variability, and central tendencies, informing subsequent analytical decisions.
Conclusion
The descriptive statistical analysis of the clinical trial data demonstrates the potential effectiveness of the new medication in lowering cholesterol levels and improving related biomarkers. The systematic calculation of measures such as mean, median, standard deviation, and range offers valuable insights into the treatment response. These results support further detailed analyses to explore causality and clinical significance, ultimately contributing to evidence-based practice in managing high cholesterol and associated metabolic disorders.
References
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