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Updated: Sep 16, 2025

Psychophysiological Assessment of the Effectiveness of Emotion Regulation Strategies in Childhood
Published on: February 11, 2017
How to measure negative effects of psychological interventions
Alexander Rozental1, Tomáš Řiháček2
1Department of Health, Education and Technology, Luleå University of Technology, Sweden; Department of Clinical Neuroscience, Karolinska Institute, Sweden.
Negative effects of psychological interventions are often overlooked. This review emphasizes patient-reported outcomes and improved monitoring for better patient safety and treatment transparency.
Area of Science:
- Psychology
- Clinical Psychology
- Psychotherapy Research
Background:
- Negative effects of psychological interventions (e.g., deterioration, non-response, new symptoms) are ethically and clinically significant but underexamined.
- Current assessment methods often rely on symptom deterioration, which is insufficient.
- There is a need for more direct, patient-reported measures to capture adverse outcomes.
Purpose of the Study:
- To review current methods for assessing negative effects in psychological interventions.
- To highlight limitations of existing assessment approaches.
- To provide recommendations for improved monitoring and reporting of adverse events.
Main Methods:
- Review of current literature on assessing negative effects of psychological interventions.
- Description and comparison of eight commonly used assessment instruments.
- Discussion of methodological challenges in assessing negative effects.
Main Results:
- Existing methods for assessing negative effects are limited, particularly those relying solely on symptom deterioration.
- Eight instruments were reviewed, showing variability in content, coverage, and psychometric properties.
- Methodological challenges include assessment timing, measurement reactivity, and patient disclosure reluctance.
Conclusions:
- Improved monitoring and reporting of negative effects are crucial for ethical practice and patient safety.
- Recommendations focus on transparency, patient-reported outcomes, and inclusive research practices.
- Further research is needed to develop and validate comprehensive measures for adverse effects in diverse populations and treatments.
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