Executive Summary

Key Chi-Square Test Findings

OV

Executive Summary

Chi-Square Test Key Findings

0
P-Value

Executive Summary — overview — High-level chi-square test results and key findings

0
p value
TRUE
significant
0.405
cramers v
Medium
effect magnitude
65.59
chi squared
200
sample size

Business Context

Company: Test Corp

Objective: Test independence between treatment type and outcome

Summary

Statistic Value
Chi-squared 65.589
Degrees of Freedom 4
P-value 1.93e-13
Cramér's V 0.405
Effect Size Medium
IN

Key Insights

Executive Summary

  1. Statistically Significant Association: The chi-square test results indicate a p-value of 1.93e-13, which is below the significance level of 0.05. This suggests a statistically significant association between treatment type and outcome.

  2. Practical Significance: The Cramér’s V effect size of 0.4049 indicates a medium effect magnitude. This signifies that the association between treatment type and outcome is not only statistically significant but also practically meaningful in terms of effect size.

  3. Key Business Implications: The significant association between treatment type and outcome highlights the importance of selecting the appropriate treatment for desired outcomes. Understanding and leveraging this association can lead to more effective treatment strategies, potentially enhancing overall outcomes and optimizing resource allocation within the company, Test Corp. The medium effect size emphasizes the practical relevance of these findings, suggesting tangible benefits in decision-making processes regarding treatments and their expected outcomes.

IN

Key Insights

Executive Summary

  1. Statistically Significant Association: The chi-square test results indicate a p-value of 1.93e-13, which is below the significance level of 0.05. This suggests a statistically significant association between treatment type and outcome.

  2. Practical Significance: The Cramér’s V effect size of 0.4049 indicates a medium effect magnitude. This signifies that the association between treatment type and outcome is not only statistically significant but also practically meaningful in terms of effect size.

  3. Key Business Implications: The significant association between treatment type and outcome highlights the importance of selecting the appropriate treatment for desired outcomes. Understanding and leveraging this association can lead to more effective treatment strategies, potentially enhancing overall outcomes and optimizing resource allocation within the company, Test Corp. The medium effect size emphasizes the practical relevance of these findings, suggesting tangible benefits in decision-making processes regarding treatments and their expected outcomes.

RC

Recommendations

Actionable Insights

Recommendations — recommendations — Actionable insights and next steps

TRUE
significant
Medium
effect magnitude
FALSE
expected warning
Placebo - No Effect
max contribution cell

Business Context

Company: Test Corp

Objective: Test independence between treatment type and outcome

IN

Key Insights

Recommendations

Based on the data analysis results for Test Corp, here are 3 actionable recommendations:

  1. Treatment Efficacy Assessment: Given the statistically significant medium effect size observed with the treatments (Drug A, Drug B, and Placebo) on different outcomes (Mild Effect, No Effect, Strong Effect), it is recommended to conduct a detailed assessment of the efficacy of Drug A and Drug B compared to the Placebo. Further studies to understand the specific effects of each drug on different outcomes could provide valuable insights for treatment optimization.

  2. Optimization of Treatment: Based on the findings that the Placebo exhibited no effect, it is recommended to focus on optimizing the treatments (Drug A and Drug B) to enhance their effectiveness. Investigating factors influencing treatment response and exploring potential synergistic effects between the drugs could help in improving overall patient outcomes and treatment success rates.

  3. Clinical Decision Making: Incorporate the results of the independence test between treatment type and outcome into clinical decision-making processes. Ensure that healthcare providers are aware of the varying effects of the treatments on different outcomes to make informed decisions regarding patient care. Providing guidelines or protocols based on these findings can help in personalized treatment selection for better patient response.

  4. Further Research and Development: Consider investing in further research and development to explore new treatment options or modifications to existing treatments based on the outcomes of this study. Investigate alternative approaches to address the limitations of current treatments and potentially enhance patient outcomes in the context of Test Corp’s objectives.

IN

Key Insights

Recommendations

Based on the data analysis results for Test Corp, here are 3 actionable recommendations:

  1. Treatment Efficacy Assessment: Given the statistically significant medium effect size observed with the treatments (Drug A, Drug B, and Placebo) on different outcomes (Mild Effect, No Effect, Strong Effect), it is recommended to conduct a detailed assessment of the efficacy of Drug A and Drug B compared to the Placebo. Further studies to understand the specific effects of each drug on different outcomes could provide valuable insights for treatment optimization.

  2. Optimization of Treatment: Based on the findings that the Placebo exhibited no effect, it is recommended to focus on optimizing the treatments (Drug A and Drug B) to enhance their effectiveness. Investigating factors influencing treatment response and exploring potential synergistic effects between the drugs could help in improving overall patient outcomes and treatment success rates.

  3. Clinical Decision Making: Incorporate the results of the independence test between treatment type and outcome into clinical decision-making processes. Ensure that healthcare providers are aware of the varying effects of the treatments on different outcomes to make informed decisions regarding patient care. Providing guidelines or protocols based on these findings can help in personalized treatment selection for better patient response.

  4. Further Research and Development: Consider investing in further research and development to explore new treatment options or modifications to existing treatments based on the outcomes of this study. Investigate alternative approaches to address the limitations of current treatments and potentially enhance patient outcomes in the context of Test Corp’s objectives.

Statistical Test Results

Chi-Square Analysis

TR

Statistical Test Results

Chi-Square Statistics

5
Significance

Statistical Test Results test_results Detailed chi-square test statistics and conclusions

Statistic Value
Chi-squared 65.589
Degrees of Freedom 4
P-value 1.93e-13
Cramér's V 0.405
Effect Size Medium
65.59
chi squared
4
df
IN

Key Insights

Statistical Test Results

The chi-square test results indicate a statistically significant relationship between the treatment type and the treatment outcome (p-value = 1.9339e-13 < 0.05). This means that the variables “treatment” and “outcome” are associated, rather than independent.

Given the high chi-squared value of 65.5887 and the low p-value, we can reject the null hypothesis that there is no relationship between the treatment type and outcome. Therefore, there is evidence to suggest that the treatment type significantly impacts the treatment outcome.

Additionally, the Cramér’s V value of 0.405 indicates a medium effect size, further supporting the association between treatment type and outcome. This effect size suggests that there is a moderate relationship between the variables.

In business terms, these results imply that the choice of treatment (Drug A, Drug B, or Placebo) has a significant impact on the treatment outcome (Mild Effect, No Effect, or Strong Effect). This information can be crucial for decision-making in healthcare settings, pharmaceutical companies, or any business where treatment effectiveness is of paramount importance. A key takeaway would be to consider the specific effects of each treatment option when making decisions about patient care or product development.

IN

Key Insights

Statistical Test Results

The chi-square test results indicate a statistically significant relationship between the treatment type and the treatment outcome (p-value = 1.9339e-13 < 0.05). This means that the variables “treatment” and “outcome” are associated, rather than independent.

Given the high chi-squared value of 65.5887 and the low p-value, we can reject the null hypothesis that there is no relationship between the treatment type and outcome. Therefore, there is evidence to suggest that the treatment type significantly impacts the treatment outcome.

Additionally, the Cramér’s V value of 0.405 indicates a medium effect size, further supporting the association between treatment type and outcome. This effect size suggests that there is a moderate relationship between the variables.

In business terms, these results imply that the choice of treatment (Drug A, Drug B, or Placebo) has a significant impact on the treatment outcome (Mild Effect, No Effect, or Strong Effect). This information can be crucial for decision-making in healthcare settings, pharmaceutical companies, or any business where treatment effectiveness is of paramount importance. A key takeaway would be to consider the specific effects of each treatment option when making decisions about patient care or product development.

ES

Effect Size

Practical Significance

0.405
Cramers v

Effect Size Analysis effect_size Magnitude and practical significance

0.405
cramers v
Medium
effect magnitude
65.59
chi squared
4
df
IN

Key Insights

Effect Size

The effect size analysis reveals a Cramér’s V value of 0.4049, indicating a medium effect size. This suggests a moderately strong relationship between the treatment and outcome variables in the study.

Practically, a medium effect size like this can be considered meaningful and could have practical implications for decision-making. In this context, it implies that the difference in outcomes between the treatment groups (Drug A, Drug B, Placebo) is not just statistically significant but also of a noticeable magnitude. This effect could be important when making choices about which drug to use in a clinical setting, for example.

Additionally, the chi-squared value of 65.5887 with 4 degrees of freedom indicates that there is a statistically significant association between the treatment and outcome variables beyond what would be expected by chance alone.

Therefore, while statistical significance tells us whether an effect is likely to be real or just due to random chance, the effect size (like Cramér’s V) helps us understand the practical importance of that effect. In this case, a medium effect size suggests that the relationship between treatment and outcome is not only statistically significant but also substantial enough to influence decision-making in a meaningful way.

IN

Key Insights

Effect Size

The effect size analysis reveals a Cramér’s V value of 0.4049, indicating a medium effect size. This suggests a moderately strong relationship between the treatment and outcome variables in the study.

Practically, a medium effect size like this can be considered meaningful and could have practical implications for decision-making. In this context, it implies that the difference in outcomes between the treatment groups (Drug A, Drug B, Placebo) is not just statistically significant but also of a noticeable magnitude. This effect could be important when making choices about which drug to use in a clinical setting, for example.

Additionally, the chi-squared value of 65.5887 with 4 degrees of freedom indicates that there is a statistically significant association between the treatment and outcome variables beyond what would be expected by chance alone.

Therefore, while statistical significance tells us whether an effect is likely to be real or just due to random chance, the effect size (like Cramér’s V) helps us understand the practical importance of that effect. In this case, a medium effect size suggests that the relationship between treatment and outcome is not only statistically significant but also substantial enough to influence decision-making in a meaningful way.

Contingency Table Analysis

Observed Frequencies

CA

Contingency Table

Observed Frequencies

3
Count

Contingency Table Analysis — Observed frequencies and patterns

3
n rows
3
n cols
200
n total
IN

Key Insights

Contingency Table

The contingency table data provided shows the observed frequencies of different outcomes (Mild, No Effect, Strong Effect) for three treatments (Drug A, Drug B, Placebo).

  1. Observed Frequency Patterns:

    • Drug A: Has the highest frequency for Mild and Strong effects but lower for No Effect.
    • Drug B: Shows a higher frequency for Strong Effect compared to Mild and No Effect.
    • Placebo: Has the highest frequency for No Effect, while the frequencies for Mild and Strong effects are lower.
  2. Notable Concentrations or Gaps:

    • Drug A and Drug B both have concentrations towards the Strong Effect category, with Drug B having the highest frequency in this category.
    • Placebo has a concentration towards the No Effect category, with the highest frequency in this category compared to the other treatments.
  3. Implications of Frequency Patterns:

    • The relationship between the treatment type and outcomes is evident. Drug A and Drug B seem to be more effective in producing Strong Effects compared to the Placebo.
    • Placebo, on the other hand, seems to have a higher rate of No Effect outcomes compared to the other treatments.
    • Understanding these patterns can help in evaluating the effectiveness of each treatment in producing different levels of effects and can guide decision-making in healthcare interventions.
IN

Key Insights

Contingency Table

The contingency table data provided shows the observed frequencies of different outcomes (Mild, No Effect, Strong Effect) for three treatments (Drug A, Drug B, Placebo).

  1. Observed Frequency Patterns:

    • Drug A: Has the highest frequency for Mild and Strong effects but lower for No Effect.
    • Drug B: Shows a higher frequency for Strong Effect compared to Mild and No Effect.
    • Placebo: Has the highest frequency for No Effect, while the frequencies for Mild and Strong effects are lower.
  2. Notable Concentrations or Gaps:

    • Drug A and Drug B both have concentrations towards the Strong Effect category, with Drug B having the highest frequency in this category.
    • Placebo has a concentration towards the No Effect category, with the highest frequency in this category compared to the other treatments.
  3. Implications of Frequency Patterns:

    • The relationship between the treatment type and outcomes is evident. Drug A and Drug B seem to be more effective in producing Strong Effects compared to the Placebo.
    • Placebo, on the other hand, seems to have a higher rate of No Effect outcomes compared to the other treatments.
    • Understanding these patterns can help in evaluating the effectiveness of each treatment in producing different levels of effects and can guide decision-making in healthcare interventions.

Residuals Analysis

Identifying Key Associations

RA

Standardized Residuals

Cell Contributions to Association

Placebo - No Effect
Max Residual

Standardized Residuals — Identify cells contributing to association

Placebo - No Effect
max contribution cell
25.34
max contribution pct
IN

Key Insights

Standardized Residuals

Based on the analysis of the standardized residuals, we observe that the combination of “Placebo” treatment with “No Effect” outcome contributes the most to the chi-square statistic with a contribution percentage of 25.34%. This means that the interaction between the placebo treatment and no effect outcome is significantly strong and is driving the association within the dataset.

The cell “Placebo - No Effect” in the contingency table has a standardized residual of 4.08, which is the highest among all cells. This indicates that the observed frequency of the combination of placebo treatment and no effect outcome is significantly higher than what would be expected if there was no association between treatment and outcome. This suggests that there might be a real effect of the placebo treatment leading to no effect outcomes, highlighting the importance of further investigating this specific combination.

Understanding which combinations contribute most to the chi-square statistic and identifying the cells that are driving the association is crucial in analyzing the relationship between treatment and outcomes in this scenario. This information can help researchers focus their attention on specific combinations that are potentially more influential in explaining the overall association observed in the data. Further investigations into these specific combinations can provide valuable insights into the effectiveness of different treatments and their respective outcomes.

IN

Key Insights

Standardized Residuals

Based on the analysis of the standardized residuals, we observe that the combination of “Placebo” treatment with “No Effect” outcome contributes the most to the chi-square statistic with a contribution percentage of 25.34%. This means that the interaction between the placebo treatment and no effect outcome is significantly strong and is driving the association within the dataset.

The cell “Placebo - No Effect” in the contingency table has a standardized residual of 4.08, which is the highest among all cells. This indicates that the observed frequency of the combination of placebo treatment and no effect outcome is significantly higher than what would be expected if there was no association between treatment and outcome. This suggests that there might be a real effect of the placebo treatment leading to no effect outcomes, highlighting the importance of further investigating this specific combination.

Understanding which combinations contribute most to the chi-square statistic and identifying the cells that are driving the association is crucial in analyzing the relationship between treatment and outcomes in this scenario. This information can help researchers focus their attention on specific combinations that are potentially more influential in explaining the overall association observed in the data. Further investigations into these specific combinations can provide valuable insights into the effectiveness of different treatments and their respective outcomes.

Effect Size & Contributions

Practical Significance

CC

Cell Contributions

Percentage Contribution to Chi-Square

Placebo - No Effect
Max %

Cell Contributions — Contribution of each cell to chi-square statistic

Placebo - No Effect
max contribution cell
25.34
max contribution pct
IN

Key Insights

Cell Contributions

From the provided data on cell contributions to the chi-square statistic, we see that the combination “Placebo - No Effect” has the highest contribution percentage of 25.34%. This cell stands out as the most responsible for the association observed in the data.

Insights:

  1. Placebo - No Effect: This combination stands out due to its significantly higher contribution percentage compared to other cells. It indicates that the observation of “No Effect” with the placebo treatment is a major driver of the chi-square statistic, suggesting a strong association between the placebo treatment and the lack of effect.

  2. Drug B - Strong Effect: Another noteworthy combination is “Drug B - Strong Effect” with a contribution percentage of 21.18%. This suggests that the observation of a strong effect with Drug B also plays a significant role in the association observed in the data.

  3. Contributions by Drug A: While Drug A has contributions across all effect levels, none stand out as much as the “Placebo - No Effect” combination. This could indicate that the lack of effect with Drug A is not as influential in the association as the lack of effect seen with the placebo.

  4. Residuals: The residuals for each cell indicate the deviation of observed values from expected values. Cells with high residuals indicate a larger than expected contribution to the chi-square statistic, highlighting associations between specific treatments and outcomes.

These insights point towards specific treatment-outcome combinations that are driving the observed association. Further analysis could explore why these particular cells are more pronounced in their contributions and what implications they have for the overall study or experiment.

IN

Key Insights

Cell Contributions

From the provided data on cell contributions to the chi-square statistic, we see that the combination “Placebo - No Effect” has the highest contribution percentage of 25.34%. This cell stands out as the most responsible for the association observed in the data.

Insights:

  1. Placebo - No Effect: This combination stands out due to its significantly higher contribution percentage compared to other cells. It indicates that the observation of “No Effect” with the placebo treatment is a major driver of the chi-square statistic, suggesting a strong association between the placebo treatment and the lack of effect.

  2. Drug B - Strong Effect: Another noteworthy combination is “Drug B - Strong Effect” with a contribution percentage of 21.18%. This suggests that the observation of a strong effect with Drug B also plays a significant role in the association observed in the data.

  3. Contributions by Drug A: While Drug A has contributions across all effect levels, none stand out as much as the “Placebo - No Effect” combination. This could indicate that the lack of effect with Drug A is not as influential in the association as the lack of effect seen with the placebo.

  4. Residuals: The residuals for each cell indicate the deviation of observed values from expected values. Cells with high residuals indicate a larger than expected contribution to the chi-square statistic, highlighting associations between specific treatments and outcomes.

These insights point towards specific treatment-outcome combinations that are driving the observed association. Further analysis could explore why these particular cells are more pronounced in their contributions and what implications they have for the overall study or experiment.

Analytics Statistical Hypothesis Testing Chi Square: CELL_CONTRIBUTIONS

Slide configuration not found

Proportions Analysis

Distribution Patterns

PA

Proportions Analysis

Distribution by Category

3
Proportions

Proportions Analysis — Row and column percentage distributions

3
n rows
3
n cols
IN

Key Insights

Proportions Analysis

The proportions analysis provided focuses on the distribution patterns within rows and columns for treatments (Drug A, Drug B, Placebo) and outcomes (Mild Effect, No Effect, Strong Effect).

Distribution within Rows (Treatments):

  1. Drug A:

    • Mild Effect: 47.54%
    • No Effect: 21.31%
    • Strong Effect: 31.15% This shows that Drug A has the highest proportion of patients experiencing a Mild Effect compared to No Effect or Strong Effect.
  2. Drug B:

    • Mild Effect: 17.74%
    • No Effect: 24.19%
    • Strong Effect: 58.06% Notably, Drug B has a significantly higher proportion of patients experiencing a Strong Effect compared to Mild or No Effect.
  3. Placebo:

    • Mild Effect: 18.18%
    • No Effect: 71.43%
    • Strong Effect: 10.39% The Placebo group has a predominance of patients with No Effect, with a relatively low percentage experiencing a Strong Effect.

Distribution within Columns (Outcomes):

  1. Mild Effect:

    • Proportion for Drug A: 53.7%
    • Proportion for Drug B: 20.37%
    • Proportion for Placebo: 25.93% The majority of patients with Mild Effect were observed in Drug A, followed by Placebo and then Drug B.
  2. No Effect:

    • Proportion for Drug A: 15.66%
    • Proportion for Drug B: 18.07%
    • Proportion for Placebo: 66.27% A high proportion of patients with No Effect belong to the Placebo group, with lower percentages for Drug A and B.
  3. Strong Effect:

    • Proportion for Drug A: 30.16%
    • Proportion for Drug B: 57.14%
    • Proportion for Placebo: 12.7% Drug B stands out with the highest proportion of patients experiencing a Strong Effect, followed by Drug A and then Placebo.

Associations:

  • The data suggests an association between the type of drug and the effect observed, with each drug showing distinct patterns in the distribution of effects.
  • Drug B appears to have a higher likelihood of causing a Strong Effect
IN

Key Insights

Proportions Analysis

The proportions analysis provided focuses on the distribution patterns within rows and columns for treatments (Drug A, Drug B, Placebo) and outcomes (Mild Effect, No Effect, Strong Effect).

Distribution within Rows (Treatments):

  1. Drug A:

    • Mild Effect: 47.54%
    • No Effect: 21.31%
    • Strong Effect: 31.15% This shows that Drug A has the highest proportion of patients experiencing a Mild Effect compared to No Effect or Strong Effect.
  2. Drug B:

    • Mild Effect: 17.74%
    • No Effect: 24.19%
    • Strong Effect: 58.06% Notably, Drug B has a significantly higher proportion of patients experiencing a Strong Effect compared to Mild or No Effect.
  3. Placebo:

    • Mild Effect: 18.18%
    • No Effect: 71.43%
    • Strong Effect: 10.39% The Placebo group has a predominance of patients with No Effect, with a relatively low percentage experiencing a Strong Effect.

Distribution within Columns (Outcomes):

  1. Mild Effect:

    • Proportion for Drug A: 53.7%
    • Proportion for Drug B: 20.37%
    • Proportion for Placebo: 25.93% The majority of patients with Mild Effect were observed in Drug A, followed by Placebo and then Drug B.
  2. No Effect:

    • Proportion for Drug A: 15.66%
    • Proportion for Drug B: 18.07%
    • Proportion for Placebo: 66.27% A high proportion of patients with No Effect belong to the Placebo group, with lower percentages for Drug A and B.
  3. Strong Effect:

    • Proportion for Drug A: 30.16%
    • Proportion for Drug B: 57.14%
    • Proportion for Placebo: 12.7% Drug B stands out with the highest proportion of patients experiencing a Strong Effect, followed by Drug A and then Placebo.

Associations:

  • The data suggests an association between the type of drug and the effect observed, with each drug showing distinct patterns in the distribution of effects.
  • Drug B appears to have a higher likelihood of causing a Strong Effect

Assumptions & Validity

Test Requirements Check

AS

Assumptions Check

Test Validity

3
Status

Assumptions Check assumptions Validation of chi-square test assumptions

Mild Effect No Effect Strong Effect
16.470 25.320 19.220
16.740 25.730 19.530
20.790 31.950 24.250
16.47
min expected
FALSE
expected warning
IN

Key Insights

Assumptions Check

Based on the provided data profile, we can see that the minimum expected frequency is 16.47, which indicates that the chi-square test assumptions are met as all expected frequencies are greater than or equal to 5. Additionally, there are no cells with frequencies below 5, which further supports the validity of the assumptions.

If the assumptions were violated, for example, if there were cells with expected frequencies below 5, this would indicate potential issues with the reliability of the chi-square test results. In such cases, alternative statistical tests or adjustments such as merging categories or increasing sample size could be considered to address the violation of assumptions and ensure the accuracy of the analysis.

Overall, since the assumptions for the chi-square test appear to be met in this case, the results obtained from the analysis can be considered valid and reliable for drawing conclusions about the relationship between treatment and outcome categories in the study.

IN

Key Insights

Assumptions Check

Based on the provided data profile, we can see that the minimum expected frequency is 16.47, which indicates that the chi-square test assumptions are met as all expected frequencies are greater than or equal to 5. Additionally, there are no cells with frequencies below 5, which further supports the validity of the assumptions.

If the assumptions were violated, for example, if there were cells with expected frequencies below 5, this would indicate potential issues with the reliability of the chi-square test results. In such cases, alternative statistical tests or adjustments such as merging categories or increasing sample size could be considered to address the violation of assumptions and ensure the accuracy of the analysis.

Overall, since the assumptions for the chi-square test appear to be met in this case, the results obtained from the analysis can be considered valid and reliable for drawing conclusions about the relationship between treatment and outcome categories in the study.

EC

Expected Frequencies

Under Independence Hypothesis

3
Min Expected

Expected vs Observed expected_comparison Compare expected frequencies under independence

Mild Effect No Effect Strong Effect
16.470 25.320 19.220
16.740 25.730 19.530
20.790 31.950 24.250
16.47
min expected
FALSE
expected warning
IN

Key Insights

Expected Frequencies

The largest deviations from expected values can provide insights into the nature of the association between treatments and outcomes.

  1. For Drug A and Mild Effect:

    • Expected: 16.47
    • Observed: 29
    • Deviation: 12.53 (Observed - Expected)
    • Insight: There is a notable higher-than-expected frequency of mild effects for Drug A. This suggests that Drug A might be associated with a stronger impact on mild effects compared to what would be expected under independence.
  2. For Drug B and Strong Effect:

    • Expected: 19.53
    • Observed: 36
    • Deviation: 16.47 (Observed - Expected)
    • Insight: There is a substantial higher-than-expected frequency of strong effects for Drug B. This indicates that Drug B might have a significant association with producing strong effects compared to what would be anticipated under independence.

These deviations from expected frequencies highlight potential associations between specific treatments and outcomes that are stronger than what would occur by chance, suggesting possible relationships between the treatments and the observed effects. Further analysis could explore the significance and implications of these associations within the context of the study.

IN

Key Insights

Expected Frequencies

The largest deviations from expected values can provide insights into the nature of the association between treatments and outcomes.

  1. For Drug A and Mild Effect:

    • Expected: 16.47
    • Observed: 29
    • Deviation: 12.53 (Observed - Expected)
    • Insight: There is a notable higher-than-expected frequency of mild effects for Drug A. This suggests that Drug A might be associated with a stronger impact on mild effects compared to what would be expected under independence.
  2. For Drug B and Strong Effect:

    • Expected: 19.53
    • Observed: 36
    • Deviation: 16.47 (Observed - Expected)
    • Insight: There is a substantial higher-than-expected frequency of strong effects for Drug B. This indicates that Drug B might have a significant association with producing strong effects compared to what would be anticipated under independence.

These deviations from expected frequencies highlight potential associations between specific treatments and outcomes that are stronger than what would occur by chance, suggesting possible relationships between the treatments and the observed effects. Further analysis could explore the significance and implications of these associations within the context of the study.

Association Visualization

Visual Patterns

MP

Association Visualization

Mosaic Plot

0.405
Cramér's V

Association Visualization — Visual representation of categorical association

0.405
cramers v
0
p value
IN

Key Insights

Association Visualization

The association visualization is a mosaic plot representing the association between different treatments (Drug A, Drug B, Placebo) and outcomes (Mild Effect, No Effect, Strong Effect).

  • Visual Patterns indicating Association or Independence:

    • In the mosaic plot, if the tiles are proportional to the frequencies of the categories, we can observe that the size of each tile varies based on the frequency of each combination of treatment and outcome. The pattern in the mosaic plot shows how the treatments are distributed across the different outcomes.
    • If the tiles were not proportional and showed a specific non-random pattern (like one treatment being more prevalent for a particular outcome), it would indicate an association between the treatment and outcome variables.
  • Interpretation in Practical Terms:

    • A Cramér’s V value of 0.4049 and a p-value of 1.9339e-13 suggest a strong association between the treatment and outcome variables. This means that the choice of treatment significantly affects the outcome observed.
    • The mosaic plot would likely show non-random patterns, such as certain treatments being more effective for specific outcomes compared to others. This could have crucial implications for medical decisions, indicating which treatment is more likely to result in a mild, no, or strong effect.

In summary, the association visualization would demonstrate how the treatments are associated with different outcomes, highlighting the effectiveness of each treatment option in causing mild, no, or strong effects.

IN

Key Insights

Association Visualization

The association visualization is a mosaic plot representing the association between different treatments (Drug A, Drug B, Placebo) and outcomes (Mild Effect, No Effect, Strong Effect).

  • Visual Patterns indicating Association or Independence:

    • In the mosaic plot, if the tiles are proportional to the frequencies of the categories, we can observe that the size of each tile varies based on the frequency of each combination of treatment and outcome. The pattern in the mosaic plot shows how the treatments are distributed across the different outcomes.
    • If the tiles were not proportional and showed a specific non-random pattern (like one treatment being more prevalent for a particular outcome), it would indicate an association between the treatment and outcome variables.
  • Interpretation in Practical Terms:

    • A Cramér’s V value of 0.4049 and a p-value of 1.9339e-13 suggest a strong association between the treatment and outcome variables. This means that the choice of treatment significantly affects the outcome observed.
    • The mosaic plot would likely show non-random patterns, such as certain treatments being more effective for specific outcomes compared to others. This could have crucial implications for medical decisions, indicating which treatment is more likely to result in a mild, no, or strong effect.

In summary, the association visualization would demonstrate how the treatments are associated with different outcomes, highlighting the effectiveness of each treatment option in causing mild, no, or strong effects.

Technical Details

Complete Analysis Summary

TD

Technical Details

Methodology & Parameters

65.59
Details

Technical Details — Complete statistical output and methodology

65.59
chi squared
4
df
0
p value
0.05
alpha
Pearson's Chi-squared test
method

Cell analysis

Cell Observed Expected Residual Contribution_Pct
Drug A - Mild Effect 29.000 16.470 3.090 14.530
Drug B - Mild Effect 11.000 16.740 -1.400 3.000
Placebo - Mild Effect 14.000 20.790 -1.490 3.380
Drug A - No Effect 13.000 25.320 -2.450 9.130
Drug B - No Effect 15.000 25.730 -2.120 6.820
Placebo - No Effect 55.000 31.950 4.080 25.340
Drug A - Strong Effect 19.000 19.220 -0.050 0.000
Drug B - Strong Effect 36.000 19.530 3.730 21.180
Placebo - Strong Effect 8.000 24.250 -3.300 16.610
IN

Key Insights

Technical Details

Technical Details: Pearson’s Chi-squared Test

Test Methodology:

  • Purpose: To determine if there is an association between the treatment (row variable) and outcome (column variable) categories.
  • Test Statistic: Pearson’s chi-squared test was used.
  • Chi-squared Value: 65.5887
  • Degrees of Freedom (df): 4
  • p-value: 1.9339e-13 (p < 0.05, significant)
  • Significance Level (α): 0.05

Degrees of Freedom Calculation:

Degrees of freedom (df) are calculated as: df = (Number of rows - 1) * (Number of columns - 1) In this case, df = (3 - 1) * (3 - 1) = 2 * 2 = 4

Considerations & Limitations:

  • The chi-squared test assumes all observations are independent and that the sample size is adequate.
  • The test is valid when the expected frequency in each cell is at least 5, though this assumption may be relaxed with larger sample sizes.
  • The test is based on categorical data and may not account for potential confounding variables or causation.

Cell Analysis:

  • The table provides observed and expected frequencies for each cell, along with residual values (observed minus expected) and their contribution percentages.
  • Residuals show how far observed counts deviate from expected counts, indicating areas with potential over/underrepresentation.
  • Contribution percentages highlight the proportional impact of each cell on the overall chi-squared statistic.

Conclusion:

The statistically significant chi-squared value suggests a significant association between treatment type and outcome. Further analysis could explore the nature and strength of this association and its implications for the studied variables.

IN

Key Insights

Technical Details

Technical Details: Pearson’s Chi-squared Test

Test Methodology:

  • Purpose: To determine if there is an association between the treatment (row variable) and outcome (column variable) categories.
  • Test Statistic: Pearson’s chi-squared test was used.
  • Chi-squared Value: 65.5887
  • Degrees of Freedom (df): 4
  • p-value: 1.9339e-13 (p < 0.05, significant)
  • Significance Level (α): 0.05

Degrees of Freedom Calculation:

Degrees of freedom (df) are calculated as: df = (Number of rows - 1) * (Number of columns - 1) In this case, df = (3 - 1) * (3 - 1) = 2 * 2 = 4

Considerations & Limitations:

  • The chi-squared test assumes all observations are independent and that the sample size is adequate.
  • The test is valid when the expected frequency in each cell is at least 5, though this assumption may be relaxed with larger sample sizes.
  • The test is based on categorical data and may not account for potential confounding variables or causation.

Cell Analysis:

  • The table provides observed and expected frequencies for each cell, along with residual values (observed minus expected) and their contribution percentages.
  • Residuals show how far observed counts deviate from expected counts, indicating areas with potential over/underrepresentation.
  • Contribution percentages highlight the proportional impact of each cell on the overall chi-squared statistic.

Conclusion:

The statistically significant chi-squared value suggests a significant association between treatment type and outcome. Further analysis could explore the nature and strength of this association and its implications for the studied variables.