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A Transdiagnostic, Self-guided Internet Intervention ("Velibra") for Waitlist Patients With Anxiety Disorders

Charité University Medicine Berlin logo

Charité University Medicine Berlin

Status

Enrolling

Conditions

Panic Disorder With Agoraphobia
Panic Disorder Without Agoraphobia
Generalized Anxiety Disorder
Social Anxiety Disorder

Treatments

Behavioral: Velibra

Study type

Interventional

Funder types

Other

Identifiers

NCT04793828
EA 1/322/19

Details and patient eligibility

About

The project's aim is to investigate the effect of a transdiagnostic, self-guided, internet-based cognitive behavioral therapy program in waitlist patients with anxiety disorders.

Full description

Patients who fulfill the inclusion criteria and are interested in psychotherapy are offered participation in the study to bridge the waiting time for face-to-face psychotherapy. After obtaining informed consent, a pre-treatment assessment is conducted. Then, participants are provided access to velibra, an internet-based cognitive behavioral therapy program which they can work through at their own pace. While velibra is a self-guided program, participants are supported by study personnel during four assessments at four time points: pre-treatment, mid-treatment (after the first three velibra modules), post-treatment and at the one-month follow-up. The investigators expect improvements on the primary as well as the secondary outcomes. Furthermore, the investigators are interested in studying the acceptability of velibra and whether positive changes already become observable after the first three modules, i.e., at the mid-treatment assessment.

Enrollment

30 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Diagnosis of panic disorder with or without agoraphobia, social anxiety disorder, or generalized anxiety disorder
  • Knowledge of German that is sufficient for engaging with the treatment and responding to the questionnaires
  • Written informed consent
  • Internet access

Exclusion criteria

  • Diagnoses of severe mental comorbidities (e.g., schizophrenia, severe major depression, borderline personality disorder)
  • Acute suicidality
  • Started or changed anxiolytic pharmacotherapy recently (currently or in the past four weeks)

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

30 participants in 1 patient group

Intervention (velibra)
Experimental group
Description:
Arm consisting of participants who receive velibra, an internet-based cognitive behavioral therapy program.
Treatment:
Behavioral: Velibra

Trial contacts and locations

1

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Central trial contact

Lena Pyrkosch, Dipl.-Psych.; Anna Wehrheim, M.Sc.-Psych.

Data sourced from clinicaltrials.gov

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