Community Based Group Psychoeducation for Relatives of Individuals With Mental Illness

NCT06190262 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 744

Last updated 2025-03-28

No results posted yet for this study

Summary

The goal of this one-arm pre-test/post-test study is to evaluate the feasibility and preliminary effect of a community-based psychoeducational group intervention for informal caregivers of individuals with mental illness.

The main questions it aims to answer are:

* What is the feasibility and acceptability of the intervention?
* What is the preliminary effect of the intervention?

Participants self-select to the intervention and participation in the evaluation is voluntary. Participants will be asked to:

* Answer a questionnaire before and after their participation
* Some participants will be invited for an in-depth interview

There is no comparison group, but feasibility and acceptability will also be explored by asking the implementation team (e.g. project leaders and teachers) to participate in:

* In-depth interviews
* Answering shorter questionnaires about provider acceptability

Conditions

  • Caregiver Burden
  • Caregiver Burnout
  • Well-Being, Psychological
  • Coping Strategies
  • Knowledge, Attitudes, Practice

Interventions

BEHAVIORAL

The intervention is community based group psychoeducation

The intervention is community based group psychoeducation

Sponsors & Collaborators

  • Region of Southern Denmark

    collaborator OTHER
  • OPEN, Open Patient data Explorative Network, Odense University Hospital, Region of Southern Denmark

    collaborator UNKNOWN
  • University of Southern Denmark

    lead OTHER

Principal Investigators

  • Rikke Amalie Agergaard Jensen, Ph.d. · Department of Regional Health Research, University of Southern Denmark

Study Design

Allocation
NA
Purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2024-01-08
Primary Completion
2025-01-30
Completion
2025-01-30

Countries

  • Denmark

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06190262 on ClinicalTrials.gov