- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06865573
Youth Mental Health Recovery in the Family After Inpatient Stay (ReCoVer)
Reintegration, Coping, and Care of Families After Inpatient Child and Adolescent Psychiatric Treatment
The goal of this longitudinal mixed-methods study is to investigate caregiver strain, family processes and health outcomes after youth psychiatric inpatient treatment. Caregivers of youth who received inpatient treatment for mental health problems will complete a survey at three timepoints (baseline, 3- and 6- month followup) reporting on youth outcomes, caregiver well-being, and family processes. Qualitative interviews on caregivers' challenges, needs, and resources around the return to home care are conducted with a subsample (target n = 10) of participants.
The main research questions (RQs) are:
RQ 1: Do family processes contribute to youth mental health outcomes after discharge from inpatient treatment? RQ 1a: What family-level risk factors predict youth readmission to inpatient treatment? RQ 1b: Do family processes predict youth mental health trajectories over time? RQ 2: Is there a reciprocal relationship between youth mental health problems and caregiver burden? RQ 2a: Do family processes mediate the association between caregiver burden and youth mental health problems? RQ 3: How do caregivers experience their children's return to home care? RQ 3a: What challenges and needs do caregivers report? RQ 3b: What types of follow-up services do families receive and/or have access to? RQ 3c: How do caregivers cope with ongoing difficulties in the post-discharge period?
Study Overview
Status
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Amos-Silvio E Friedrich
- Phone Number: +43 1-4277-47286
- Email: amos.friedrich@univie.ac.at
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- 18 years or older
- primary caregiver of a child or adolescent aged 7-21 years of any gender who received inpatient treatment in a psychiatric institution in Germany, Austria, or Switzerland (min. 24 h stay) within the past month (regardless of the diagnosis or the reason for the treatment, respectively)
- lived with the child or adolescent in the same household since discharge
Exclusion Criteria:
- another caregiver of the same child has already participated in the study
- insufficient knowledge of German
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
|---|
|
caregivers
primary caregivers of youth who received inpatient psychiatric treatment
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Youth mental health
Time Frame: Change from baseline (T0) to 3-month (T1) and 6-month (T2) follow-up
|
Caregiver-reported youth internalizing and externalizing problems (assessed using the Pediatric Symptom Checklist)
|
Change from baseline (T0) to 3-month (T1) and 6-month (T2) follow-up
|
|
Inpatient readmission
Time Frame: Within 6 months
|
Occurrence (and admission date) of inpatient mental health treatment after discharge
|
Within 6 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Youth health-related quality of life
Time Frame: Change from baseline (T0) to 3-month (T1) and 6-month (T2) follow-up
|
Quality of life related to self-esteem, school, and peer relationships (assessed using the KINDL-R)
|
Change from baseline (T0) to 3-month (T1) and 6-month (T2) follow-up
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Martina Zemp, Professor, University of Vienna
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 01291
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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