Higher Outdoor Temperature Predicts Moderately Higher Chest Pains for Population
Contents

Variables

A
Outdoor Temperature 454
A
Chest Pains 113

Categories

A
Environment 564
A
Symptoms 13336

Tags

High Confidence
Weak Effect Size
Positive Relationship
Population Study
cause image gauge image effect image
Participants reported a 29.8% average increase in Chest Pains following above average Outdoor Temperature.

Abstract

Chest Pains was generally 43.7% higher than average after 26.1 degrees celsius of Outdoor Temperature per 7 days.

Aggregated data from 1 study participants suggests with a HIGH degree of confidence (p=0.001, 95% CI -0.062 to 0.686) that Outdoor Temperature has a moderately positive predictive relationship (R=0.312) with Chest Pains.

The highest quartile of Chest Pains measurements were observed following an average 27.1 degrees celsius Outdoor Temperature.

The lowest quartile of Chest Pains measurements were observed following an average 26.2 degrees celsius of Outdoor Temperature.

After an onset delay of 0 seconds, Chest Pains is typically 21% lower than average over the 7 days following around 26.2 degrees celsius of Outdoor Temperature Outdoor Temperature.

Keywords: Outdoor Temperature, Chest Pains, N-of-1 trials, real-world evidence, causal inference, observational study

Preliminary: Based on 1 participants. Results may change as more data is collected.

Results

Primary Findings

Analysis of 60 paired observations from 1 participants revealed a substantial improvement in Chest Pains following above-average Outdoor Temperature exposure.

+43.7%
Change from Baseline
Substantial effect on Chest Pains
0.03
Predictor Impact Score
Insufficient evidence for causal relationship

Supporting Statistics

Low
Confidence
0.312
Correlation (r)
p = 0.356
Significance
z = 1.21
Effect Magnitude
φ = 1.00
Temporality

What This Means

When participants had above-average Outdoor Temperature:

  • Chest Pains increased by 43.7% on average
  • Temporal analysis supports Outdoor Temperature as the predictor (not the outcome)

Interpreting the Predictor Impact Score

The Predictor Impact Score (PIS) integrates multiple Bradford Hill causal criteria into a single metric. Use this guide to interpret the score:

PIS Range Interpretation Recommended Action
≥ 0.5 Strong evidence High priority for RCT validation
0.3 - 0.5 Moderate evidence Consider for experimental investigation
0.1 - 0.3 Weak evidence Monitor for additional data
< 0.1 Insufficient evidence Low priority; may be noise

Note: PIS is a prioritization heuristic, not proof of causation. High scores indicate relationships worth investigating, not confirmed causal effects. With only 1 participants, these scores are preliminary and will become more reliable as additional data is collected.

Optimal Daily Values

No clear dose-response relationship detected. The Outdoor Temperature values associated with high and low Chest Pains are too similar to provide meaningful dosing guidance. This may indicate a threshold effect (any amount works equally well), no effect, or insufficient data variance. With more participants, a clearer pattern may emerge.

Population Correlation

Outdoor Temperature Distribution

Chest Pains Distribution

Statistical Summary

Relationship Statistics

Property Value
Cause Variable Name Outdoor Temperature
Effect Variable Name Chest Pains
Sinn Predictive Coefficient 0.029690726185371
Confidence Level HIGH
Confidence Interval 0.37372
Forward Pearson Predictive Coefficient 0.312
Critical T Value 1.671
Average Outdoor Temperature Over Previous 7 days Before ABOVE Average Chest Pains 27.1 degrees celsius
Average Outdoor Temperature Over Previous 7 days Before BELOW Average Chest Pains 26.2 degrees celsius
Duration of Action 7 days
Effect Size moderately positive
Number of Paired Measurements 60
Optimal Pearson Product 0.15042142904657
P Value 0.001
Statistical Significance 0.3557
Strength of Relationship 0.37372
Study Type population
Analysis Performed At 2026-01-04
Number of Participants 1

Outdoor Temperature Info

Property Value
Variable Name Outdoor Temperature
Aggregation Method MEAN
Analysis Performed At 2020-09-15
Duration of Action 7 days
Kurtosis 2.5869393546724
Maximum Allowed Value 101 degrees celsius
Mean 16.934805022738 degrees celsius
Median 16.806543406516 degrees celsius
Minimum Allowed Value -66 degrees celsius
Number of Aggregate Predictors 0
Number of Aggregate Outcomes 454
Number of Measurements 312494
Number of Measurements (including those generated by tagged, joined, or child variables) 60483
Public true
Onset Delay 0 seconds
Standard Deviation 5.8976135603379
Unit Degrees Celsius
User Variables 927
UPC 0
Variable Category Environment
Variable ID 5954773
Variance 55.947734908476

Chest Pains Info

Property Value
Variable Name Chest Pains
Aggregation Method MEAN
Analysis Performed At 2020-10-09
Duration of Action 24 hours
Kurtosis 1.74195801105
Maximum Allowed Value 5 out of 5
Mean 2.43042 out of 5
Median 2.4 out of 5
Minimum Allowed Value 1 out of 5
Number of Aggregate Predictors 102
Number of Aggregate Outcomes 11
Number of Measurements 60
Number of Measurements (including those generated by tagged, joined, or child variables) 60
Public true
Onset Delay 0 seconds
Standard Deviation 0.41741844344941
Unit 1 to 5 Rating
User Variables 14
UPC 0
Variable Category Symptoms
Variable ID 87136
Variance 0.40391577060932

Introduction

Background

Outdoor Temperature (Environment) and Chest Pains (Symptoms) are both important factors in understanding human health and well-being. This study investigates the relationship between these two variables using real-world observational data.

Traditional randomized controlled trials (RCTs), while the gold standard for causal inference, are often impractical, expensive, or unethical for studying many health relationships. Aggregated N-of-1 observational studies offer a complementary approach that leverages within-subject comparisons across large populations to identify meaningful patterns.

Research Question

Does Outdoor Temperature affect Chest Pains?

Additionally, we seek to determine:

  1. What is the direction and magnitude of any effect?
  2. How confident can we be in this relationship based on the available data?
  3. What are the optimal levels of Outdoor Temperature for maximizing Chest Pains?

Study Objective

The objective of this study is to determine the nature of the relationship (if any) between Outdoor Temperature and Chest Pains. Additionally, we attempt to determine the Outdoor Temperature values most likely to produce optimal Chest Pains values.

Study Overview

This is a population-level observational study using aggregated N-of-1 methodology. By aggregating individual N-of-1 experiments, we can identify population-level patterns while accounting for the substantial individual variation that exists in most health relationships. Effect sizes are reported as percent change from baseline, enabling intuitive interpretation and comparison across different measures.

Full Methodology: Framework for Real-World Evidence-Based Pharmacovigilance: Aggregated N-of-1 Trials for Quantifying Treatment Effects

Discussion

Interpretation of Findings

Participants experienced a 43.7% improvement in Chest Pains following above-average Outdoor Temperature exposure. The Predictor Impact Score (PIS) of 0.03 indicates insufficient evidence for a causal relationship.

Statistical Significance

Using a two-tailed t-test with alpha = 0.05, it was determined that the change in Chest Pains is statistically significant at a 95% confidence interval. The p-value of 0.3557 indicates there is less than a 35.57% probability that this result occurred by chance.

After treatment, a 29.8% increase (0.814 out of 5) from the mean baseline 1.86 out of 5 was observed. The relative standard deviation at baseline was 36.1%. The observed change was 1.2085 times the standard deviation.

A common rule of thumb considers a change greater than twice the baseline standard deviation on two separate pre-post experiments may be considered significant. This occurrence would have only a 5% likelihood of resulting from random fluctuation (a p-value < 0.05).

T-Test Details
Observed t-value: 3.639
Critical t-value: 1.671

Since t = 3.64 > 1.67, we reject the null hypothesis.

Biological Plausibility

A plausible bio-chemical mechanism between predictor and outcome is critical for interpreting observational findings. This is where human judgment excels beyond statistical analysis.

Community feedback on the biological plausibility of this relationship is still being collected. Consider the known mechanisms by which Outdoor Temperature might influence Chest Pains.

Bradford Hill Criteria Assessment

The Bradford Hill criteria provide a framework for assessing causality in observational studies. Our methodology operationalizes six of the nine criteria through the Predictor Impact Score (PIS):

Criterion How Addressed Metric
Strength Effect size magnitude Percent change from baseline (Δ%), z-score
Consistency Cross-participant replication Number of users (N), number of pairs (n)
Temporality Predictor precedes outcome Temporality factor (φ), onset delay (δ > 0)
Biological Gradient Dose-response relationship Gradient coefficient (φgradient)
Plausibility Biological mechanism assessment Community votes on mechanism plausibility
Specificity Category appropriateness Interest factor (finterest)

Predictor Impact Score (PIS)

The PIS integrates multiple Bradford Hill criteria into a composite metric quantifying how reliably a predictor affects an outcome. Higher scores indicate stronger evidence:

Population-Level PIS:

$$\text{PIS}_{\text{agg}} = |r_{\text{forward}}| \cdot w \cdot \phi_{\text{users}} \cdot \phi_{\text{pairs}} \cdot \phi_{\text{change}} \cdot \phi_{\text{gradient}}$$

Where φ-factors are saturation functions approaching 1 as evidence accumulates:

  • φusers = 1 - e-N/10 (user saturation)
  • φpairs = 1 - e-n/nsig (pair saturation)
  • φchange = 1 - espreadsig (effect spread saturation)
  • w = weighted average of plausibility votes

Temporality Assessment

We assess evidence for correct causal direction using the temporality factor:

$$\phi_{\text{temporal}} = \frac{|r_{\text{forward}}|}{|r_{\text{forward}}| + |r_{\text{reverse}}|}$$

Values approaching 1 indicate the predictor precedes the outcome (supporting causation); values near 0.5 suggest ambiguous directionality; values near 0 suggest reverse causation or confounding by indication.

Limitations

As with any observational study, correlation does not prove causation. Key limitations include:

  • Unmeasured confounders: Variables not tracked may influence results
  • Self-selection bias: Health trackers may differ from the general population
  • Measurement error: Self-reported data may contain recall bias
  • Confounding by indication: Sicker individuals may use more treatments

However, within-subject comparison and temporal precedence analysis partially mitigate these limitations. If the relationship is merely coincidental, as participants independently modify their Outdoor Temperature values, the observed strength will decline over time. Spurious correlations naturally dissipate as more data is collected.

Future Directions

Future research should examine:

  • Subgroup analyses to identify individual differences in response
  • Potential confounders and mediators of the observed relationship
  • Optimal dosing and timing for Outdoor Temperature
  • Confirmation through prospective or randomized designs
  • Biological mechanisms underlying the observed effects

Conclusion

📊 Preliminary Findings: With 1 participants, these results are based on limited data. Effect sizes and confidence will improve as more participants contribute data. Consider these findings directional rather than definitive.

Above-average Outdoor Temperature was associated with a 43.7% improvement in Chest Pains—a substantial effect. The Predictor Impact Score of 0.03 indicates this relationship is requiring additional data before conclusions.

Bottom Line: Based on a PIS of 0.03 and a 43.7% effect size, this relationship currently lacks sufficient evidence. Continue monitoring as more data becomes available. Note: These conclusions may strengthen or change direction as more data is collected.

These findings contribute to our understanding of how Outdoor Temperature may influence Chest Pains in real-world conditions. While preliminary, these results may inform future research directions. As more participants contribute data, the reliability and precision of these findings will improve substantially.

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Methods

Study Design

This study is based on data donated by 1 participants. Thus, the study design is equivalent to the aggregation of 1 separate n=1 observational natural experiments.

This within-subject design is powerful because it controls for all stable individual characteristics (genetics, baseline health status, socioeconomic factors) that might otherwise confound the relationship between variables.

Data Analysis

Temporal Assumptions

The analysis incorporates temporal assumptions about the relationship between variables:

  • Onset Delay: It was assumed that 0 seconds would pass before a change in Outdoor Temperature would produce an observable change in Chest Pains.
  • Duration of Action: It was assumed that Outdoor Temperature could produce an observable change in Chest Pains for as much as 7 days after the stimulus event.

Statistical Methods

For each participant, we calculated the Pearson correlation coefficient between Outdoor Temperature values and subsequent Chest Pains values. Individual correlations were then aggregated using Fisher's z-transformation to produce a population-level estimate:

Individual Correlation:

$$r_i = \frac{\sum(x_{ij} - \bar{x}_i)(y_{ij} - \bar{y}_i)}{\sqrt{\sum(x_{ij} - \bar{x}_i)^2 \sum(y_{ij} - \bar{y}_i)^2}}$$

Fisher's Z-Transformation:

$$z_i = \frac{1}{2} \ln\left(\frac{1 + r_i}{1 - r_i}\right)$$

Aggregated Correlation:

$$\bar{r} = \tanh(\bar{z}) \quad \text{where} \quad \bar{z} = \frac{1}{N}\sum_{i=1}^{N} z_i$$

Effect Size Calculation

Effect sizes are reported as percent change from baseline. For each participant, we compare the outcome following above-average predictor values to the overall baseline outcome:

$$\Delta\%_{\text{baseline}} = \frac{\bar{O}_{\text{follow-up}} - \bar{O}_{\text{baseline}}}{\bar{O}_{\text{baseline}}} \times 100$$

Effect Magnitude (Z-Score)

To assess effect magnitude relative to natural variability, we calculate the z-score:

$$z = \frac{|\Delta\%_{\text{baseline}}|}{\text{RSD}_{\text{baseline}}}$$

where RSDbaseline is the relative standard deviation of outcome during baseline period

A z-score > 2 indicates statistical significance (p < 0.05), meaning the observed change exceeds typical baseline fluctuation and is unlikely due to random variation.

Statistical Significance

Correlation significance is assessed using a two-tailed t-test:

$$t = \frac{r\sqrt{n-2}}{\sqrt{1-r^2}}$$

We reject the null hypothesis (ρ = 0) at α = 0.05 when |t| exceeds the critical value, providing statistical evidence that the observed relationship is not due to chance.

Data Sources

Outdoor Temperature data was primarily collected using Weather. Automatically import temperature, humidity, and ultraviolet light exposure.

Chest Pains data was primarily collected using QuantiModo. QuantiModo allows you to easily track mood, symptoms, or any outcome you want to optimize in a fraction of a second. You can also import your data from over 30 other apps and devices. QuantiModo then analyzes your data to identify which hidden factors are most likely to be influencing your mood or symptoms.

Data Quality

Data quality measures were applied to ensure reliable results:

  • Minimum Data Requirement: Only participants with sufficient paired observations were included in the analysis.
  • Outlier Handling: Extreme values were winsorized to reduce the influence of measurement errors.
  • Missing Data: Days with missing values were handled using appropriate filling strategies based on the variable type.
  • Test User Exclusion: Test accounts and invalid users were excluded from all analyses.

Principal Investigator

Program & Methods

Mike P. Sinn

Designed and implemented data collection, aggregation, causal inference pipeline, and automated study generation framework. Developed the Predictor Impact Score methodology operationalizing Bradford Hill criteria for ranking causal relationships in observational data. When he tells people this at parties, they usually say they have to go check on their car.

Individual study outputs are automated, reproducible, and open to external audit. (Which I would seriously recommend.)

Cite This Study

APA Format
Sinn, M. P. (2026). Causal Analysis: Does Outdoor Temperature Affect Chest Pains?. The Journal of Citizen Science. https://studies.crowdsourcingcures.org/study/cause-5954773-effect-87136-population-study
BibTeX
@misc{sinn_cause_5954773_effect_87136_population_study_2026,
  author = {Sinn, Mike P.},
  title = {Causal Analysis: Does Outdoor Temperature Affect Chest Pains?},
  year = {2026},
  publisher = {The Journal of Citizen Science},
  url = {https://studies.crowdsourcingcures.org/study/cause-5954773-effect-87136-population-study},
  note = {Accessed: January 10, 2026}
}
Chicago/Turabian
Sinn, Mike P. "Causal Analysis: Does Outdoor Temperature Affect Chest Pains?." The Journal of Citizen Science. Accessed January 10, 2026. https://studies.crowdsourcingcures.org/study/cause-5954773-effect-87136-population-study.
Harvard
Sinn, M.P., 2026. Causal Analysis: Does Outdoor Temperature Affect Chest Pains?. [Aggregated N-of-1 Study] The Journal of Citizen Science. Available at: https://studies.crowdsourcingcures.org/study/cause-5954773-effect-87136-population-study [Accessed January 10, 2026].

Study Type: Aggregated N-of-1 Observational Mega-Study
Evidence Level: Level II (Real-World Evidence)
Methodology: Bradford Hill Criteria with Predictor Impact Score (PIS)

References

This framework was originally developed in 2013 based on the Bradford Hill criteria. Subsequent literature has independently validated similar approaches to causal inference from observational data:

  1. Hill, A.B. (1965). The environment and disease: association or causation? Proceedings of the Royal Society of Medicine, 58(5), 295-300. [Bradford Hill criteria]
  2. Lillie, E.O., et al. (2011). The n-of-1 clinical trial: the ultimate strategy for individualizing medicine? Personalized Medicine, 8(2), 161-173. [N-of-1 methodology]
  3. Pearl, J. (2009). Causality: Models, Reasoning, and Inference . Cambridge University Press. [Causal inference]
  4. Hernán, M.A., & Robins, J.M. (2020). Causal Inference: What If . Chapman & Hall/CRC. [Free textbook]
  5. FDA (2018). Framework for FDA's Real-World Evidence Program . U.S. Food and Drug Administration. [Regulatory context]
  6. Duan, N., et al. (2013). Single-patient (n-of-1) trials: a pragmatic clinical decision methodology . Journal of Clinical Epidemiology, 66(8), S21-S28.
  7. Platt, R., et al. (2018). The FDA Sentinel Initiative—an evolving national resource . New England Journal of Medicine, 379(22), 2091-2093.

This information is for research and educational purposes only, not medical advice. Consult a healthcare provider before making health decisions. Terms of Service