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Caregiver BurdenReCoVerNCT06865573

Youth Mental Health Recovery in the Family After Inpatient Stay

An observational study of Caregiver Burden and Family Characteristics, run by University of Vienna.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
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Trial summary

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… Read more about this study

Who is it for?
Ages 18 years and older
How many people
70 participants
Where
No sites listed yet
Study dates
May 2025to Apr 2026
Phase
Observational
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: primary caregivers (parents or guardians regardless of the biological relationship to the child) of children and adolescents who received inpatient psychiatric treatment

Who may be able to join

  • 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

Who cannot join

  • another caregiver of the same child has already participated in the study
  • insufficient knowledge of German

Trial locations and contacts

No sites are listed yet. Contact the study team or a site near you to ask about taking part.

Amos-Silvio E Friedrich contact

+43 1-4277-47286

amos.friedrich@univie.ac.at

About this study

Official title: 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?

Medical subject headings
Caregiver Burden

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT06865573
Study groupRoleWhat they receive
caregiversprimary caregivers of youth who received inpatient psychiatric treatment

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Inpatient readmission

    Occurrence (and admission date) of inpatient mental health treatment after discharge

    Measured: Within 6 months

  2. Youth mental health

    Caregiver-reported youth internalizing and externalizing problems (assessed using the Pediatric Symptom Checklist)

    Measured: Change from baseline (T0) to 3-month (T1) and 6-month (T2) follow-up

Secondary outcomes (1)
  1. Youth health-related quality of life

    Quality of life related to self-esteem, school, and peer relationships (assessed using the KINDL-R)

    Measured: Change from baseline (T0) to 3-month (T1) and 6-month (T2) follow-up

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted10 Mar 2025
  2. Study startMay 2025 (estimated)
  3. Primary completionApr 2026 (estimated)
  4. Study completionApr 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
70 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06865573
Sponsor's protocol ID
01291
Acronym
ReCoVer
Status last verified
Mar 2025
First submitted
5 Mar 2025
Last updated
17 Mar 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Publications

  • Friedrich AE, Zemp M. Youth post-discharge recovery and family adjustment after inpatient mental health treatment - study protocol for the longitudinal mixed-methods ReCoVer study. Front Child Adolesc Psychiatry. 2026 Aug 7;5:1605414. doi: 10.3389/frcha.2026.1605414. eCollection 2026.

    PubMed 42630289

Questions about this trial

What is this clinical trial studying?

An observational study of Caregiver Burden and Family Characteristics, run by University of Vienna.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: opening soon, as of the sponsor's last update on 17 Mar 2025. Status can change between updates, so confirm with the study contact before making plans.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Amos-Silvio E Friedrich (+43 1-4277-47286, amos.friedrich@univie.ac.at), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Inpatient readmission (time frame: Within 6 months). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT06865573, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 17 Mar 2025.

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