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Post-COVID group psychotherapy to strengthen the resilience of individuals with neuropsychiatric post-COVID-symptoms

Post-COVID group psychotherapy to strengthen the resilience of individuals with neuropsychiatric post-COVID-symptoms - POCO-study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00036588
Enrollment
100
Registered
2025-11-24
Start date
2025-07-17
Completion date
Unknown
Last updated
2025-12-08

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: Post-COVID Experimental Group: Group Psychotherapy with a focus on psychoeducation (8 sessions of 90 minutes each within 8 weeks, plus 1 pre- and 1 post-test session of 90 minutes each, total

Sponsors

Universitätsklinikum Frankfurt, Klinik für Psychiatrie, Psychosomatik und Psychotherapie
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: •Diagnosis of neuropsychiatric symptoms in the context of post-COVID-syndrome according to WHO criteria (ICD-10 U09.9; WHO, 2019). •Age between 18 and 65 •Patients who are able to work/not on sick leave and patients who are unable to work/on sick leave during the intervention phase •Sufficient knowledge of German •Outpatients •Stable antidepressant medication in the last 4 weeks before the start of the intervention

Exclusion criteria

Exclusion criteria: •Acute suicidality •Current severe depressive episode •Current psychotic symptoms or history of psychotic symptoms •Bipolar disorder •Current substance use, substance dependence, or substance abuse •Antisocial, schizotypal, or borderline personality disorder •Other primary diagnosis according to ICD-10 (WHO, 2021) •Other ongoing psychotherapy •Serious somatic problems that prevent attendance at group therapy sessions or serious internal medical conditions •Any other severe neurological disease, current or in the past (e.g., condition after cerebral hemorrhage, cerebral ischemia, dementia, multiple sclerosis, severe traumatic brain injury) •Pregnancy or breastfeeding •Individuals who are dependent on or employed by the investigator

Design outcomes

Primary

MeasureTime frame
Assessment of chronic exhaustion and work-related stress tolerance, measured with the Chandler Fatigue Scale (Martin et al., 2010), the Fatigue Impact Scale (FIS; Fisk et al., 1994) , and the psychosocial dimension of the Fatigue Severity Scale (FSS; Krupp et al., 1989), the Quality of Life Scale (German version of the WHOQOL-BREF; WHO, 2012), the German version of the Occupational Depression Inventory (ODI; Bianchi & Schonfeld, 2020), the Work Ability Index (WAI; Freyer, Formazin & Rose, 2019), the Return to Work Attitude Self-efficacy Questionnaire (RTW-SE), and the Effort-Reward-Imbalance Questionnaire (ERI; Siegrist et al., 2016); assessed before and after group psychotherapy (pre-/post-test session)

Secondary

MeasureTime frame
Symptom reduction, measured using the German version of the Montgomery-Asberg Depression Scale (MADRS; Montgomery & Asberg, 1979), the German version of the Quick Inventory of Depressive Symptomatology (QIDS SR-16; Rush et al., 2003), and the Scale for Dysfunctional Depressive Cognitions (DAS; Hautzinger et al., 1983) and the Patient Health Questionnaire-D (PHQ-D; Löwe, 2015); assessed before and after group psychotherapy (pre-/post-test session) Number of sick days at work; assessed before group psychotherapy (pre-test session) and after 10 weeks (post-test session)

Countries

Germany

Contacts

Public ContactViola Oertel

Universitätsklinikum Frankfurt, Klinik für Psychiatrie, Psychosomatik und Psychotherapie

viola.oertel@unimedizin-ffm.de+49 (69) 6301 83780

Outcome results

None listed

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