ClinicalTrials.Veeva

Menu

Internet-administered Interpersonal Psychotherapy for Depressive Symptoms

L

Linköping University (LiU)

Status

Completed

Conditions

Major Depressive Disorder

Treatments

Behavioral: Interpersonal psychotherapy

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

The aim of the study is to test the efficacy of a treatment for depression based on interpersonal psychotherapy (IPT). The treatment will be accessed via an internet platform built for this study. A therapist will provide support weekly, as well as on-demand when needed. The treatment lasts for 10 weeks.

Enrollment

113 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • A diagnosis of Major depressive disorder (as indicated by the MINI 7.0 Neuropsychiatric interview) and/or depressive symptoms equal to or more severe than mild depression on the MADRS-S (equal to or above 13 points) and/or BDI (equal to or above 14 points).
  • Age of at least 18 years old.
  • Adequate ability to speak, write, and read Swedish.
  • Internet access for the duration of the study.

Exclusion criteria

  • Ongoing substance abuse.
  • Suicidal plans.
  • A diagnosed personality syndrome (as diagnosed before the study by a licensed psychiatric healthcare professional).
  • Other ongoing psychological treatment.
  • Other severe psychiatric comorbidity that requires specialized care (e.g. anorexia nervosa, psychosis).
  • Recent changes in psychotropic medication or planned changes during the initial treatment period.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

113 participants in 2 patient groups

Interpersonal psychotherapy (IPT)
Experimental group
Description:
10 weeks of internet-administered interpersonal psychotherapy with therapist support.
Treatment:
Behavioral: Interpersonal psychotherapy
Wait-list control group
No Intervention group
Description:
The participants in the control group will receive access to the treatment after the post-treatment assessment has been conducted.

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems