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Optimizing threat expectancy change during exposure therapy for anxiety disorders

Optimizing threat expectancy change during exposure therapy for anxiety disorders

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00036318
Enrollment
50
Registered
2026-06-25
Start date
2025-05-06
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

F40.0 F40.1 F40.2 F41.0

Interventions

Group 1: Active Comparator: Manualized exposure-based cognitive behavioral therapy with 15 double-sessions (incl. psychoeducation, exposure, self-management, booster) Group 2: Experimental group: Manu

Sponsors

Georg-August-Universität Göttingen
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 69 Years

Inclusion criteria

Inclusion criteria: Primary diagnosis of panic disorder, agoraphobia, social anxiety disorder, or specific phobia according to DSM-5. At least mild anxiety symptom severity (PROMIS-Anxiety = 20). Outpatient status (i.e., outpatient psychotherapy with weekly sessions for 12 weeks and booster sessions possible). Sufficient German language skills. Informed consent.

Exclusion criteria

Exclusion criteria: Acute suicidality. Current or history of bipolar disorder, psychotic disorder, or borderline personality disorder. Current alcohol, medication, or drug dependence (except nicotine and caffeine; abstinence should be > 6 months). Severe medical conditions that prevent regular participation in therapy or bias research question (e.g., brain damage). Any other general contraindications for exposure or psychotherapy (see Pittig & Pittig, 2024). Any other reason endangering adherence to treatment protocol (e.g., planned inpatient treatment, planned absence or relocation, etc.). Concomitant psychotherapy (inpatient or outpatient). Concomitant psychopharmacological treatment is permitted, provided there has been no change in medication type or dosage during the 3 months prior to study entry.

Design outcomes

Primary

MeasureTime frame
Exposure-related learning rate based on als exposure exercises from the first three exposure sessions, assessed via patient report of threat expectancy, threat occurence, and adjusted threat expectancy (see Pittig et al., 2023)

Secondary

MeasureTime frame
Threat expectancy change from the exposure sessions via patient report assessed via patient report of threat expectancy and adjusted threat expectancy (see Pittig et al., 2023)

Countries

Germany

Contacts

Public ContactAndre Pittig

Universität Göttingen

andre.pittig@uni-goettingen.de+49-551-39-29022

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Aug 10, 2026