# Testing for a General Changepoint in Medical and Psychometric Studies: Changes Detection and Sample Size Planning

**Authors:** Nicoletta D'Angelo

PMC · DOI: 10.1002/sim.70150 · Statistics in Medicine · 2025-06-13

## TL;DR

This paper introduces a new and simple method for detecting changes in data from medical and psychometric studies, which also helps in planning how much data to collect.

## Contribution

The paper introduces a new change detection method using a pseudo Score statistic with known distributions for easy power and sample size calculations.

## Key findings

- The proposed method outperforms existing change point tests in simulations with normal and binary data.
- The method is applied successfully to genomic and SAT data, showing practical utility.
- The new test is available as an R package and a Shiny App for user accessibility.

## Abstract

This paper introduces a new method for change detection in medical and psychometric studies based on the recently introduced pseudo Score statistic, for which the sampling distribution under the alternative hypothesis has been determined. Our approach has the advantage of simplicity in its computation, eliminating the need for resampling or simulations to obtain critical values. Additionally, it comes with known null and alternative distributions, facilitating easy calculations for power levels and sample size planning. The paper indeed also discusses the topic of power analysis in segmented regression, namely the estimation of sample size or power level when the study data being collected focuses on a covariate expected to affect the mean response via a piecewise relationship with an unknown breakpoint. We run simulation studies showing that our method outperforms other Tests for a Change Point (TFCP) with both normally distributed and binary data and carry out two real data analyses on genomic data and SAT critical reading data. The proposed test contributes to the framework of medical and psychometric research, and it is available on the Comprehensive R Archive Network (CRAN) and in a more user‐friendly Shiny App, both illustrated at the end of the paper.

## Full-text entities

- **Diseases:** TFCP (MESH:D013736), tumor (MESH:D009369)
- **Cell lines:** GM01524 — Homo sapiens (Human), Developmental delay, Finite cell line (CVCL_X249)

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12166113/full.md

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12166113/full.md

## References

44 references — full list in the complete paper: https://tomesphere.com/paper/PMC12166113/full.md

---
Source: https://tomesphere.com/paper/PMC12166113