Actively Recruiting

Phase Not Applicable
Age: 18Years - 75Years
All Genders
Healthy Volunteers
NCT06514495

Differential Effects of in Vivo and Virtual Exposure Therapy in Agoraphobia

Led by Johannes Gutenberg University Mainz · Updated on 2025-09-03

68

Participants Needed

1

Research Sites

117 weeks

Total Duration

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AI-Summary

What this Trial Is About

Anxiety disorders, including agoraphobia, are prevalent in the German population, leading affected individuals to avoid specific places like crowds or public transport. Although cognitive-behavioral therapy with exposure is an effective treatment, many patients resort to medication rather than therapy. Virtual Reality Exposure Therapy (VRET) shows promise in easing exposure treatment with customizable scenarios. Interoception (body symptom perception) and the endocannabinoid system are explored as factors in maintaining agoraphobia. Studies investigate how therapies like exposure (both in vivo and in VR) impact these factors and treatment outcomes. Interoception, especially in panic disorder patients, plays a crucial role, with accurate heartbeat perception linked to maintaining anxiety. The endocannabinoid system, affecting various functions, is studied for its role in therapy outcomes and its modulation of the body's stress response. The study aims to understand how these systems interact in agoraphobic patients and how therapy affects their functionality.

CONDITIONS

Official Title

Differential Effects of in Vivo and Virtual Exposure Therapy in Agoraphobia

Who Can Participate

Age: 18Years - 75Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosis of agoraphobia with or without panic disorder (experimental group)
  • Diagnosis of social phobia (clinical control group)
  • Healthy individuals without acute or chronic mental illness (control group)
  • Depressive disorder allowed as a comorbid diagnosis in experimental and clinical control groups
Not Eligible

You will not qualify if you...

  • Other mental illnesses: substance dependence, schizophrenia, bipolar disorder, dementia, eating disorders, PTSD, major depressive episode, personality disorder
  • Somatic diseases: cancer, cardiovascular diseases, epilepsy, autoimmune diseases, metabolic or endocrine diseases
  • Taking psychotropic medication (except antidepressants), medication affecting the cardiovascular system (e.g., beta-blockers), cortisone medications, or corticosteroid creams
  • Pregnancy or breastfeeding
  • Ongoing psychotherapy

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University Medical Center

Mainz, Germany, 55122

Actively Recruiting

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Research Team

V

Vanessa Renner, Dr.

CONTACT

K

Katja Petrowski, Prof.

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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