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Interpersonal Psychotherapy for Groups adapted for the Ugandan Population: A randomized controlled trial of six sessions versus eight sessions of trigger concordant and trigger discordant therapy

Interpersonal Psychotherapy for Groups adapted for the Ugandan Population: A randomized controlled trial of six sessions versus eight sessions of trigger concordant and trigger discordant therapy

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
PACTR
Registry ID
PACTR202306771120632
Enrollment
300
Registered
2023-06-13
Start date
2022-09-01
Completion date
Unknown
Last updated
2026-08-03

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

6 SESSIONS trigger concordant weekly Interpersonal Therapy for Groups sessions
8 trigger discordant weekly Interpersonal Therapy for Groups sessions

Sponsors

StrongMinds
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Persons aged 18 years and over screened using the PHQ-9 and reported to have depression (cut off score of 10 and above on the PHQ-9), with two or more triggers of depression. Participants with at least two similar triggers out of the four IPT triggers to depressions will be included in the study. Participants must be fluent in either English or Luganda and be able to consent to participation.

Exclusion criteria

Exclusion criteria: Persons who state or carry reports indicating a previous diagnosis of intellectual disability, psychiatric disorder other than depression, or dementia, and those who are physically too unwell to participate in the interview will be excluded. Participants who meet the inclusion criteria but have impairments that hinder engagement with the research procedures for any reasons (is deaf or hard of hearing, speech, and visual impairment with no aids to see, unable to give consent will be excluded. Those who are not fluent in either spoken English or Luganda, Those under the age of 18, will also be excluded from the study. Study sites will be located in Luganda-speaking regions. Potential participants will receive a participant study information sheet or a verbal description of the study by any of the research assistants, according to their preference, and any of their questions will be answered. Written consent will be sought. Only those who give written informed consent will be recruited to the study.

Design outcomes

Primary

MeasureTime frame
PHQ-9 score change between pre- and post-intervention

Secondary

MeasureTime frame
WHOQOL-BREF score change between pre- and post-intervention ;WHODAS 2.0 score change between pre- and post-intervention

Countries

Uganda

Contacts

Public ContactPETER BIRUNGI

STRONGMINDS GLOBAL

peter.birungi@strongminds.org+256701342849

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Aug 9, 2026