Recruiting

Psychoeducational Intervention for Families With a Member Affected by Major Depression

Major depressive disorder (MDD) is the most common mental disorder. It can be a huge burden not only for the person affected by it, but also for his/her whole family. The goal of this clinical trial is to test the efficacy of a family supportive intervention called psychoeducational family intervention (PFI) compared to a brief informative intervention in families with a member affected by MDD. Families will participate in one of the two interventions for a period of 6 months more or less, and they will be asked…

ClinicalTrials.gov IDNCT05988333
PhaseNA
Enrollment384
SponsorUniversity of Campania Luigi Vanvitelli
Age18 Years
SexALL
I'm interested View official listing

Conditions studied

Depressive Disorder, Major

About this study

Major depressive disorder (MDD) is the most common mental disorder. It can be a huge burden not only for the person affected by it, but also for his/her whole family. The goal of this clinical trial is to test the efficacy of a family supportive intervention called psychoeducational family intervention (PFI) compared to a brief informative intervention in families with a member affected by MDD. Families will participate in one of the two interventions for a period of 6 months more or less, and they will be asked to answer some questionnaires about how much MDD impacts on their everyday life and the patient's symptoms, in order to understand whether a more structured intervention such as PFI can be useful for families in order to better deal with this complicated illness.

Interventions

Primary outcomes

Eligibility information

Inclusion Criteria: * diagnosis of major depression, according to Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition; * ability to provide informed consent; * presence of at least one contact per month with the psychiatric clinic for at least six months prior to recruitment; * cohabitation with at least one family member. Exclusion Criteria: * moderate or severe cognitive deficits, physical illnesses preventing the participation to the sessions or if they were hospitalization in the two months prior the enrollment

Study locations

Before you participate: Varda Clinical is an independent discovery tool, not the study sponsor or a medical provider. Eligibility can only be determined by the official study team. Discuss potential risks and benefits with a qualified healthcare professional.

Source: ClinicalTrials.gov. Record last refreshed by Varda Clinical: 2026-09-27.