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Interpersonal Psychotherapy for university students with depressive symptoms

Interpersonal Psychotherapy for University Students with Depressive Symptoms: A Feasibility Pilot Randomized Controlled Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
PACTR
Registry ID
PACTR202511612887270
Enrollment
60
Registered
2025-11-13
Start date
2025-10-20
Completion date
Unknown
Last updated
2026-09-14

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

Conditions

Mental and Behavioural Disorders

Interventions

Interpersonal Psychotherapy Adapted for Ethiopia

Sponsors

Assegid Negash
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: The inclusion criteria are as follows: ? Being a full-time undergraduate student ? Students whose Patient Health Questionnaire (PHQ-9) score range from 5-19 (mild and moderate scorers) ? Students whose age is 18 years or older ? Students who reside in WSU main campus. ? Willing to attend at least 4 IPT-E sessions with written informed consent ? Able to listen and speak the Amharic language

Exclusion criteria

Exclusion criteria: The exclusion criteria are as follows: ? Weekend, summer and postgraduate students will not be included ? Students with psychotic symptoms and severe depression (PHQ-9 score > 20) ? Students with serious conditions that will prevent them from participating in the intervention (will be measured by Mini International Neuropsychiatric Interview, MINI) ? Acute suicidality (plan and attempts) or risk of harm to others, they will be referred to the Otona hospital to get psychiatric care (will be measured by MINI) ? Students with co-morbid severe mental illness such as psychotic disorder/bipolar disorder. However, students with anxiety and somatic symptoms may not be excluded ? Students who already started counseling services or receiving psychiatric medication before the implementation of the proposed study ? Problematic substance use that impairs functioning (will be measured using Alcohol, Smoking and Substance Involvement Screening Test, ASSIST)

Design outcomes

Primary

MeasureTime frame
The primary outcomes of the study are feasibility of the intervention and clinical outcomes such as depression symptoms, functional impairment, substance use and suicidal behaviors.

Secondary

MeasureTime frame
The secondary outcomes of the study are acceptability of the intervention, appropriate to the setting, fidelity, perceived expectations, benefits and limitations of the intervention, potential facilitators and barriers to deliver the intervention.

Countries

Ethiopia

Contacts

Public ContactCharlotte Hanlon

University of Edinburgh

chanlon@ed.ac.uk+447405451626

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Sep 19, 2026