In response to a crisis of confidence, several methodological initiatives have been launched to improve the robustness of psychological science. Given its real-world implications, personality disorders research is all too important to not follow …
Data analysis in psychopathology research typically entails multiple stages of data preprocessing (e.g., coding of physiological measures), statistical decisions (e.g., inclusion of covariates), and reporting (e.g., selecting which variables best …
Open science practices, such as pre-registration and data sharing, increase transparency and may improve the replicability of developmental science. However, developmental science has lagged behind other fields in implementing open science practices. …
Science progresses by finding and correcting problems in theories. Good theories are those that help facilitate this process by being hard to vary: They explain what they are supposed to explain, they are consistent with other good theories, and they …
To increase transparency in research, the International Committee of Medical Journal Editors required, in 2005, prospective registration of clinical trials as a condition to publication. However, many trials remain unregistered or retrospectively …
Pre-registration has become an increasingly popular proposal to address concerns regarding questionable research practices. Yet preregistration does not necessarily solve these problems. It also causes additional problems, including raising costs for …
The credibility revolution in social science has led to the recommendation and adoption of practices to increase the replicability of scientific findings. Many of the recommended practices, such as replication and preregistration, present unique …
Altruism and trust lie at the heart of research on human subjects. Altruistic individuals volunteer for research because they trust that their participation will contribute to improved health for others and that researchers will minimise risks to …
In 2005, the International Committee of Medical Journal Editors (ICMJE) initiated a policy requiring investigators to deposit information about trial design into an accepted clinical trials registry before the onset of patient enrolment. 1 This …
All parties associated in clinical trials—patients, doctors, scientists, industry—share a common desire for a vigorous clinical research enterprise that brings innovations to patients as quickly as possible. However, recent scandals in the UK and …