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A Transdiagnostic Mentalization-based Intervention for Parents With Mental Disorders

NCT06315114 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 170

Last updated 2025-05-14

No results posted yet for this study

Summary

The aim of this randomised clinical trial is to evaluate the short and longterm effects of a transdiagnostic mentalization-based intervention (Lighthouse MBT Parenting Program) compared to care as usal (CAU) for parents with a mental disorder in adult mental health service.

Conditions

  • Mental Disorder
  • Behavior Disorders
  • Diagnosis, Psychiatric
  • Diagnosis Dual
  • Severe Mental Disorder
  • Mental Illness
  • Psychiatric Disorder
  • Psychiatric Disease
  • Psychiatric Illness

Interventions

BEHAVIORAL

Lighthouse MBT Parenting Program (LPP)

The experimental group is a manualized transdiagnostic mentalization-based parenting intervention (Lighthouse MBT Parenting Program). This is a 12-week parenting group intervention (weekly session of 2 hours) with one preperatory initial individual session (1 hour) before the group commence.

BEHAVIORAL

Care as usual (CAU)

1-2 next of kin sessions (called 'Familiesamtale') is considered the care as usual offered to parents in adult mental health service in the Capital Region of Denmark. Parents are offered the possibility of bringing their spouse or offspring to one of the sessions.

Sponsors & Collaborators

  • University of Copenhagen

    collaborator OTHER

  • Mental Health Services in the Capital Region, Denmark

    lead OTHER

Principal Investigators

  • Sebastian Simonsen, Doctor · Mental Health Service, Capital Region, Denmark

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-03-11
Primary Completion
2028-04-01
Completion
2028-04-01

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 NCT06315114 on ClinicalTrials.gov