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Post-COVID-19-Treatment Study

Post-COVID-19-Treatment Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00033476
Enrollment
54
Registered
2024-02-01
Start date
2024-03-05
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

U09.9

Interventions

Group 1: Cognitive-behavioral single- and group treatment (interlocked), consisting of 8 group therapy and 6 single therapy sessions, which treat psychological mechanisms of symptom maintenance (e.g.,

Sponsors

Johannes Gutenberg-Universität Mainz, Abteilung für Klinische Psychologie, Psychotherapie und Experimentelle Psychotherapie zusammen mit der Hochschulambulanz für Forschung und Lehre der Poliklinischen Institutsambulanz für Psychotherapie
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Post-COVID-Syndrom / Post-Covid-19-Condition based on WHO-criteria (2021)

Exclusion criteria

Exclusion criteria: Admission to intensive care or mechanical ventilation during COVID-19, somatic contradictions against exposure therapy, acute psychotic or manic symptoms according to DSM-5, acute substance use while fulfilling criteria of a substance use disorder (middle or severe) according to DSM-5; acute severe depressive disorder according to DSM-5, acute danger for self or others; inability to participate in sessions (physical, organizational), parallel psychotherapeutic treatment or participation in another intervention study and on-going criminal proceedings

Design outcomes

Primary

MeasureTime frame
Intensity of body complaints (incl. fatigue, breathing difficulties, circulatory problems, Post-Exertion-Symptoms) with Patient Health Questionnaire - 15 (PHQ-15), Fatigue Severity Scale (FSS), Scales "Breathing" and "Circulation" of the Symptom Burden Questionnaire - Long Covid (SBQ-LC), Scale "Post-Exertion Malaise" of the DePaul Symptom Questionnaire-2 at T0, T1, T2, T3; Symptom-related thoughts, feelings, and behaviors (symptom burden) with Somatic Symptom Disorder B - Criteria Scale (SSD-12) at T0, T1, T2, T3; Session rating with Session Rating Scale (SRS) and Group Therapy Session Evaluation form-P/T (GTS-P/T) after each single and group session; Side effects of treatment with Inventory for the balanced assessment of Negative Effects of Psychotherapy (INEP) at T1 or T2

Secondary

MeasureTime frame
Disease coping with Brief Illness Perception Questionnaire (B-IPQ) at T0, T1, T2, T3; Somatosensory Amplification with Somatosensory Amplification Scale (SSAS) at T0, T1, T2, T3; Construkts of the somatoform spectrum of the Hierarchical Taxonomy of Psychopathology (HiTOP) with short-scale for the somatoform spectrum of the HiTOP zu T0, T1, T2, T3; Treatment expectations with Credibility/Expectancy Questionnaire (CEQ) at T0; Anxiety Symptoms with Generalized Anxiety Disorder Scale-7 (GAD-7) at T0, T1, T2, T3; Depressive Symptoms with Patient Health Questionnaire-9 (PHQ-9) at T0, T1, T2, T3; Impairments of work productivity and activity with Work Productivity and Activity Impairment Questionnaire (WPAI) at T0, T1, T2, T3

Countries

Germany

Contacts

Public ContactKaroline Sophie Sauer

Johannes Gutenberg-Universität Mainz, Abteilung für Klinische Psychologie, Psychotherapie und Experimentelle Psychopathologie

karsauer@uni-mainz.de+4961313939179

Outcome results

None listed

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