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Examining the efficacy of a two-session cognitive-behavioral therapy treatment in a large group format with clinically relevant panic disorder with and without agoraphobia

Examining the efficacy of a two-session cognitive-behavioral therapy treatment in a large group format with clinically relevant panic disorder with and without agoraphobia - Don’t panic

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00035725
Enrollment
75
Registered
2024-12-12
Start date
2024-12-16
Completion date
Unknown
Last updated
2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

F41.0 F40.0

Interventions

Group 1: Two-session large group intervention, atleast 75 participants, 5 hours on day 1 and 6 hours on day 2, exposure therapy (interoceptive and situation-related)

Sponsors

Forschungs- und Behandlungszentrum der Ruhr-Universität Bochum
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: clinically relevant panic disorder with and without agoraphobia

Exclusion criteria

Exclusion criteria: Psychiatric exclusion diagnoses (I.e.: severe post-traumatic stress disorder; psychotic disorder; bipolar disorder; disorders from the schizophrenia spectrum; suicidal tendencies and seere addiction) and somatic factors (I.e.: pregnancy, severe infectious diseases, cardiopulmonary diseases, severe respiratory diseases (e.g. asthma), cardiovascular diseases, epilepsy and stroke, thyroid diseases, metabolic diseases).

Design outcomes

Primary

MeasureTime frame
1) Reduction in the severity of the symptom burden - Captured by the instruments of the AKV battery (BSQ, MI and ACQ (if agoraphobic symptoms are present)) - Collection of these measures will occur after the consultation (T0), immediately before the first day of training (T1), immediately after the first day of training (T2), immediately after the second day of training (T3) and two (T4) and six months (T5) after training 2) Remission of clinically relevant panic disorder as a result of the training - Recorded via the presence of the diagnosis “panic disorder” with and without “agoraphobia” using the Mini-DIPS: (Diagnostic Interview in Mental Disorders) at T0 and T5.

Secondary

MeasureTime frame
3) Reduction in perceived symptom burden due to training: Will be captured by the DASS (Depression-Anxiety-Stress scales). Collection of these measures will occur after the consultation (T0), immediately before the first day of training (T1), immediately after the first day of training (T2), immediately after the second day of training (T3) and two (T4) and six months (T5) after training.

Countries

Germany

Contacts

Public ContactAndré Wannemüller

Forschungs- und Behandlungszentrum der Ruhr-Universität Bochum

andre.wannemueller@rub.de+49 234 3223106

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026