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Clinical Trials in Germany / NCT06311136
Recruiting Not applicable

Effectiveness of an Ecological Momentary Emotion Regulation Intervention

NCT06311136 · tracked via the Priya Life Science Germany tracker
Phase
Not applicable
Started
2024-01-12
Last updated
2025-03-27

Condition(s) studied

Depressive Disorder, MajorPersistent Depressive DisorderHealthy

Investigational drug(s) / intervention(s)

Valence-Specific Ecological Momentary Intervention

Valence-Specific Ecological Momentary Intervention: The ecological momentary intervention is designed to enhance participants ability to select and effectively implement emotion regulation strategies fitting to the valence of their current emotions. Specifically, the intervention instructs participants to use the strategy of savoring to amplify their positive emotions, fostering an appreciation for the present moment. Conversely, for the attenuation of negative emotions, the intervention advocates to use the strategy of reappraisal, encouraging participants to reinterpret adverse situations in a more positive or neutral way, thus reducing their emotional impact. This targeted approach ensures that the emotion regulation strategies are not only effective but also contextually appropriate.

Study summary

This two-armed randomized controlled trial aims to investigate the effectiveness of an emotion regulation intervention in individuals with and without depressive disorders. The study encompasses participants diagnosed with mild to moderate major depression or persistent depressive disorder and healthy controls without a current depressive disorder.

Participants will be randomly assigned to either the intervention group, receiving a valence-specific emotion regulation intervention in daily life, or a monitoring-only control group. The valence-specific intervention supports the implementation of different emotion regulation strategies based on whether a person is experiencing mainly positive or negative emotions. In contrast, participants in the control group will solely monitor their positive and negative emotions and the strategies used to regulate them.

Outcome measures include emotion regulation ability, self-efficacy, and strategy use, depressive symptoms, positive and negative affect, and emotion beliefs (controllability, usefulness).

A second aim of the study is to compare beliefs about positive emotions and strategies to regulate them between individuals with and without current depressive disorders. Furthermore, the investigators aim to examine why individuals might choose unfavorable emotion regulation strategies even when feeling good. Therefore, another research question is, how emotion beliefs might explain emotion regulation strategy choice.

Eligibility

Sex
ALL
Min age
18 Years
Max age
65 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Online consent for participation * Adequate proficiency in the German language, encompassing both reading and comprehension skills * Ownership of a smartphone, compatible with either Android or iOS operating systems, and access to the Internet For individuals in the clinical group with current depressive disorders: * Currently meeting the DSM-5 criteria for a mild or moderate major depressive episode, or persistent depressive disorder Exclusion Criteria: * Current severe substance use disorder * Acute suicidality * Current severe major depressive episode * Lifetime bipolar disorder * Lifetime psychotic disorders For the control group, additional exclusion criteria include: * Meeting the DSM-5 criteria for a major depressive episode within the last 12 months * History of severe major depressive episodes * Recurrent depressive disorder * History of persistent depressive disorder * Current treatment (psychotherapy, pharmacotherapy) for depressive symptoms

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Department of Clinical Psychology and Psychotherapy, Institute of Psychology, Heidelberg University Heidelberg Germany Recruiting

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Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06311136 on ClinicalTrials.gov ↗ ← All trials in Germany