Actively Recruiting

Phase Not Applicable
Age: 18Years - 65Years
All Genders
Healthy Volunteers
NCT06311136

Effectiveness of an Ecological Momentary Emotion Regulation Intervention

Led by Heidelberg University · Updated on 2025-03-27

200

Participants Needed

1

Research Sites

81 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

Effectiveness of an Ecological Momentary Emotion Regulation Intervention

Who Can Participate

Age: 18Years - 65Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Online consent for participation
  • Adequate proficiency in the German language, encompassing both reading and comprehension skills
  • Ownership of a smartphone compatible with Android or iOS and internet access
  • Current diagnosis of mild or moderate major depressive episode or persistent depressive disorder (clinical group)
Not Eligible

You will not qualify if you...

  • Current severe substance use disorder
  • Acute suicidality
  • Current severe major depressive episode
  • Lifetime bipolar disorder
  • Lifetime psychotic disorders
  • Diagnosis of major depressive episode within the last 12 months (control group)
  • History of severe major depressive episodes (control group)
  • Recurrent depressive disorder (control group)
  • History of persistent depressive disorder (control group)
  • Current treatment for depressive symptoms including psychotherapy or pharmacotherapy (control group)

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Trial Site Locations

Total: 1 location

1

Department of Clinical Psychology and Psychotherapy, Institute of Psychology, Heidelberg University

Heidelberg, Germany, 69117

Actively Recruiting

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Research Team

I

Ilka Mueller, M.Sc.

CONTACT

L

Luise Pruessner, M.Sc.

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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