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IPT-based Group Intervention by Non-specialist for Improvement of Depressive Symptoms in Community Young Adults in Brazil

IPT-based Group Intervention by Non-specialist for Improvement of Depressive Symptoms in Community Young Adults in Brazil: a Randomized Clinical Trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06480019
Enrollment
50
Registered
2024-06-28
Start date
2024-03-01
Completion date
2028-12-31
Last updated
2026-04-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Depression, Interpersonal Relations

Brief summary

Major depressive disorder is a highly prevalent, recurrent, and debilitating disease, the third cause of years of lost life in the world, and it may be the most common disease in 2030, according to the World Health Organization (WHO). Furthermore, it's also related to decreased quality of life and high mortality. Interpersonal psychotherapy (IPT) is a first-line treatment and can also be used for the prevention of depression. This randomized controlled clinical trial is planned to have 50 participants randomized between an interventional and a control group (waiting list). Our study covers young adults (18 to 24 years old) with depression. Participants will be invited by social media to undergo treatment in an IPT group. The intervention group will be separated into groups with up to 10 participants, with a weekly meeting for eight weeks. The intervention will focus on interpersonal relationships within the model of IPT and will be held by a university student and a doctor trained in IPT.

Interventions

BEHAVIORALInterpersonal psychotherapy

Interpersonal psychotherapy is a first-line treatment and can also be used for the prevention of depression.

Sponsors

Hospital de Clinicas de Porto Alegre
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 24 Years
Healthy volunteers
No

Inclusion criteria

* Young adults (between 18 and 24 years old) * Young adults who work, live or study in Porto Alegre * PHQ ≥ 5 - without suicide ideation

Exclusion criteria

* Maniac or hypomanic episode * Psychotic Syndrome * Substance Abuse * Suicide Risk or Ideation

Design outcomes

Primary

MeasureTime frameDescription
Hospital Anxiety and Depression Scale (HADS)Pre-treatment, Week 1 to 8The Hospital Anxiety and Depression Scale consists of 14 items, of which 7 assess anxiety and 7 assess depression. Each item is scored from 0 to 3, and each subscale has a maximum score of 21 points with higher scores indicating greater symptom severity.

Secondary

MeasureTime frameDescription
Patient Health Questionnaire-9Pre-treatment, Week 1 to 8The PHQ-9 is a self-administered instrument that quantitatively assesses the severity of depressive symptoms over the past two weeks. It consists of nine items corresponding to the diagnostic criteria for major depressive disorder in the DSM-IV. Each item is scored on a 4-point Likert scale (0 = not at all to 3 = nearly every day), resulting in a score ranging from 0 to 27.
Social support scale (MOS-SSS)Pre-treatment, Week 1 to 8The Medical Outcomes Study Social Support Survey (MOS-SSS) measures each individual's perceptions of personal support. The scale comprises five support factors (emotional, informational, material, affective, and positive social interaction). Higher scores indicate greater perceived support.
Quality of Life (WHOQOL-BREF)Pre-treatment, Week 1 to 8The WHOQOL-BREF is a scale with 26 items that measure quality of life. It includes two general items and 24 items representing four domains (physical, psychological, social relationships, and environmental).
Clinical Global Impression (CGI)Pre-treatment, Week 1 to 8The Clinical Global Impressions (CGI) scale is an instrument that enables clinicians to assess the overall severity of the illness, the change in clinical status over time, and the effectiveness of the intervention used. Its score can range from 1 (not ill) to 7 (extremely ill).
Beck Depression Inventory (BDI)Pre-treatment; Week 1-8It's a self-report instrument and assesses the presence and severity of depressive symptoms. It consists of 21 items describing cognitive, affective, and somatic manifestations of depression. Each item is scored in a Likert scale ranging from 0 to 3, varying from 0 to 63 points

Countries

Brazil

Contacts

CONTACTNeusa Sica da Rocha, PhD
nrocha@hcpa.edu.br55(51) 3359-8000

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 14, 2026