Actively Recruiting

Phase Not Applicable
Age: 18Years - 24Years
All Genders
ID06480019

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

Age: 18Years - 24Years
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

1
2
3
+1

Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Outpatient Treatment

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

Loading map...

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

Similar Trials

The Effects of Citalopram on the Brain's Response to Emotion...

Emotional Processing

Actively Recruiting

1 location

Frequently Asked Questions

Have more questions? Get in touch with our team for quick support

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here