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implementation and scientific evaluation of a group-based intervention aimed at reducing perceived burden among informal caregivers of people with psychosis

implementation and scientific evaluation of a group-based intervention aimed at reducing perceived burden among informal caregivers of people with psychosis - PAGUS

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00037023
Enrollment
64
Registered
2025-06-27
Start date
2025-07-01
Completion date
Unknown
Last updated
2026-03-30

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

Conditions

reduction in perceived burden (MiniSCL)

Interventions

Group 1: waiting control Group 2: group intervention (=psychological support group providing information about psychosis and practical everyday strategies for dealing with affected individuals
also encourages exchange among informal caregivers)

Sponsors

BKH Augsburg
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Inclusion criteria for the affected person: The affected person has a diagnosis within the psychosis spectrum (ICD-10: F2x; F1x.5; F23). The affected person is currently or has previously been treated at a facility of the Bezirkskliniken Schwaben. The affected person has been ill for no longer than 5 years. Inclusion criteria for the informal caregiver: The informal caregiver has a valid email address (for sending the questionnaire link). The informal caregiver is able to participate in a group, i.e., has sufficient German language skills and the ability to communicate in a group setting. The informal caregiver provides written informed consent for participation in the study.

Exclusion criteria

Exclusion criteria: Exclusion criteria for the informal caregiver: Lack of capacity to consent due to a severe illness of the informal caregiver Presence of a diagnosis within the psychosis spectrum in the informal caregiver The informal caregiver is unable to attend the on-site group sessions due to mobility limitations. (There are no exclusion criteria for the affected persons.)

Design outcomes

Primary

MeasureTime frame
Perceived psychological burden as measured by the MiniSCL

Secondary

MeasureTime frame
Perceived stress, measured by the Perceived Stress Questionnaire (PSQ) Well-being, measured by the WHO-5 Self-efficacy, measured by the General Self-Efficacy Scale (SWE) Relationship quality, measured by the Quality of Relationship Inventory (QRI) perceived stigma experience (ISE) quality of life (EuroQol-5D)

Countries

Germany

Contacts

Public ContactWolfgang Strube

BKH Augsburg

wolfgang.strube@bkh-augsburg.de+49 (0) 821 4803-1021

Outcome results

None listed

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