Actively Recruiting
IPT-based Group Intervention by Non-specialist for Improvement of Depressive Symptoms in Community Young Adults in Brazil: a Randomized Clinical Trial
Led by Hospital de Clinicas de Porto Alegre · Updated on 2026-04-13
50
Participants Needed
1
Research Sites
104 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Major depressive disorder is a common, recurring, and serious condition that negatively impacts quality of life and is expected to be a leading cause of disability globally. This trial focuses on young adults aged 18 to 24 with depression, aiming to evaluate an interpersonal psychotherapy (IPT) group intervention delivered by non-specialists. The study is randomized and controlled, comparing participants receiving IPT to a waiting list control group. The intervention involves weekly group psychotherapy sessions for eight weeks, with groups of up to 10 participants. The sessions focus on improving interpersonal relationships based on the IPT model and are led by a university student and a doctor trained in IPT. Participants are recruited via social media and randomly assigned to either the treatment or waiting list group. Participants will be assessed before and during the eight weeks of treatment using several measures including the Hospital Anxiety and Depression Scale (HADS), Patient Health Questionnaire-9, Social Support Scale, Quality of Life questionnaire, Clinical Global Impression, and Beck Depression Inventory. These assessments help researchers track changes in depressive symptoms and social functioning. The trial is sponsored by Hospital de Clinicas de Porto Alegre and is planned to run until the end of 2028.
CONDITIONS
Brief Title
IPT-based Group Intervention by Non-specialist for Improvement of Depressive Symptoms in Community Young Adults in Brazil
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Young adults between 18 and 24 years old
- Young adults who work, live, or study in Porto Alegre
- PHQ score of 5 or higher without suicide ideation
You will not qualify if you...
- Maniac or hypomanic episode
- Psychotic syndrome
- Substance abuse
- Suicide risk or ideation
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 8 weeks
Participants receive interpersonal psychotherapy delivered in a group setting by non-specialists to improve depressive symptoms.
Weekly visits for up to 8 weeks
Trial Site Locations
Total: 1 location
1
Clinical Hospital for Porto Alegre
Porto Alegre, Rio Grande do Sul, Brazil, 90035-903
Actively Recruiting
Research Team
N
Neusa Sica da Rocha, PhD
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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