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NCT07432945

In Vivo Exposure vs. Videochat-Based Vicarious Exposure

Recruiting now NA Last updated 2 March 2026
What this trial tests

NA trial testing In Vivo Exposure Training (IVET) in Anxiety in 72 participants. Currently enrolling.

Timeline
26 February 2026
Primary endpoint
31 December 2026
31 December 2026

Quick facts

Lead sponsorRuhr University of Bochum
PhaseNA
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment72
Start date26 February 2026
Primary completion31 December 2026
Estimated completion31 December 2026
Sites1 location across Germany

Drugs / interventions tested

Conditions studied

Sponsor

Ruhr University of Bochum

Who can join

Adults 18 to 65, any sex, with Anxiety or Anxiety Disorders. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

After screening (including parts of the Mini-DIPS), participants will receive a pre-assessment with a baseline heartrate measurement, self-report measures and two BATs (with the treated spider and the non-treated spider). All participants receive a brief psychoeducation \& video demonstration of exposure steps. Participants are randomly assigned to the three study arms and are then set to receive a single session of either in vivo exposure (IVET), videochat based vicarious exposure (VicET) or neither (Waiting List Control, WLC). Approximately 24 hours later, the two BATs with both spiders, a slightly reduced set of self-report measures and an interview will conduct the post-assessment. The order of all BATs, the spider individuals (treated vs. non-treated spider) and assignment to study arms will be randomized using a list that will be worked through in a sequence determined using "www.random.org". At a six-week follow-up, another long-term assessment will be conducted. Here, participants will receive a brief online questionnaire related to their experiences with spiders and self-report measures that were previously administered. Participants previously assigned to the waiting list control (WLC) will be invited to participate in an in-vivo exposure session. A set of questionnaires including demographic information, VAS scales on the current psychological state and wellbeing (administered at the start and end of the first and second assessment day), the BDI-II, the STAI-T and STAI-S, FEE, SPQ, SBQ, FSQ, GSE, SEQ-SP, TC/E for treatment credibility and the "positive attitudes towards technology subscale" of the MTUA will be used. BDI-II, STAI and MTUA are only administered at pre-assessment. The SAS is used for initial screening.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Anxiety

Currently open trials in the same condition.

Other Ruhr University of Bochum trials

Trials by the same sponsor.

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Data sources for this page

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