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Clinical Trials/PACTR202306771120632
PACTR202306771120632
Completed
Phase 4

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

StrongMinds0 sites300 target enrollmentMay 17, 2023

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Mental and Behavioural Disorders
Sponsor
StrongMinds
Enrollment
300
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
May 17, 2023
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
StrongMinds

Eligibility 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

  • 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.

Outcomes

Primary Outcomes

Not specified

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