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Covid-Intervention-Study

Manual-based Psychosocial Group Interventions for Coping With the Covid-19 Pandemic and Other Crises

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05597501
Acronym
CIS
Enrollment
96
Registered
2022-10-28
Start date
2022-11-30
Completion date
2024-11-30
Last updated
2022-10-28

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

Conditions

Psychosocial Intervention

Keywords

manual-based group intervention, short-term intervention, covid-19, crisis

Brief summary

The goal of this invention study is test and compare short-term manual-based psychosocial group interventions in die Austrian population suffering from stresses and strains due to the Covid-19 Pandemic and other crises. The main question it aims to answer: Does short-term manual-based psychosocial group interventions improve the mental well-being of the participants? Participants will attend weekly a manual-based group (8 weeks) and answer online-questionnaires and surveys (pseudonymized).

Interventions

BEHAVIORALmanual-based group interventions

weekly group interventions (90min) following manuals of either CBT, integrative therapy or existential analysis&logotherapy

Sponsors

Department for Psychosomatic Medicine and Psychotherapy, University for Continuing Education Krems
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* above 18 years with psychosocial stresses and strains due to covid-19 pandemic and other crises

Exclusion criteria

* suicidal tendency * insufficient knowledge of the German language * psychotic episode * no internet-access

Design outcomes

Primary

MeasureTime frame
Positive Mental Health Scale (PMH)Screening - Start Intervention - after 8 weeks intervention - 4 months follow-up

Secondary

MeasureTime frame
Patient Health Questionnaire-9 (PHQ-9)Screening - Start Intervention - after 8 weeks intervention - 4 months follow-up
Generalized Anxiety Disorder Scale-7 (GAD-7)Screening - Start Intervention - after 8 weeks intervention - 4 months follow-up
WHO-Five Well-Being Index (WHO-5)Screening - Start Intervention - after 8 weeks intervention - 4 months follow-up
Stress Coping Inventars (SCI)Screening - Start Intervention - after 8 weeks intervention - 4 months follow-up
Pereived Stress Scale (PSS)Screening - Start Intervention - after 8 weeks intervention - 4 months follow-up
Somatic Symptome Scale-8 (SSS-8)Screening - Start Intervention - after 8 weeks intervention - 4 months follow-up

Countries

Austria

Contacts

Primary ContactCarina Dinhof, MSc.
cis@donau-uni.ac.at+43 2732 893
Backup ContactThomas Probst, Univ.Prof.Dr.
cis@donau-uni.ac.at

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026