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Randomized Controlled Trial of Trauma-focused CBT in Tanzania and Kenya

This study is ongoing, but not recruiting participants.
National Institute of Mental Health (NIMH)
Tanzania Women Research Foundation (TAWREF)
Action in the Community Environment (ACE) Africa
Information provided by (Responsible Party):
Duke University Identifier:
First received: March 25, 2013
Last updated: November 23, 2016
Last verified: November 2016

March 25, 2013
November 23, 2016
August 2012
December 2017   (Final data collection date for primary outcome measure)
Posttraumatic Stress Disorder (PTS) [ Time Frame: 15 months ]
Measured using the Child PTSD Symptoms Scale (CPSS) Caregiver and Child completed.
Same as current
Complete list of historical versions of study NCT01822366 on Archive Site
Behavioral Difficulties [ Time Frame: 15 months ]
Measured using the Child Behavior Checklist (CBCL), Youth Self-Report (YSR), and items developed locally that are culturally specific.
Same as current
  • Childhood Traumatic Grief [ Time Frame: 15 months ]
    Measured using the Inventory of Complicated Grief.
  • Depression [ Time Frame: 15 months ]
  • Child Functioning [ Time Frame: 15 months ]
    Locally developed tool used to measure functional impairment and improvement over time.
  • Child-Guardian Relationship [ Time Frame: 15 months ]
    Measured using the Child-Parent Relationship Scale (CPRS)
Same as current
Randomized Controlled Trial of Trauma-focused CBT in Tanzania and Kenya
Improving Health Outcomes by Preventing HIV/STD Risk

The primary goal is to study the effectiveness of Trauma-focused Cognitive Behavioral Therapy (TF-CBT) in treating traumatic grief and traumatic stress for orphaned children and young adolescents in two East African sites with high prevalence HIV, Moshi, Tanzania (TZ) and Bungoma, Kenya (KE), through a randomized controlled trial (RCT). In a previous feasibility study of TF-CBT with orphans in Tanzania, the investigators have found a group-based TF-CBT intervention to be feasible and acceptable, with promising clinical outcomes. In the feasibility study, lay counselors with no prior mental health experience delivered the intervention with training and supervision by our team of mental health and TF-CBT experts.

Building on this initial study, the investigators are conducting a RCT to test the effectiveness of TF-CBT for traumatic grief and traumatic stress compared to receipt of usual care orphan services in TZ and KE. The study involves collaboration with HIV/AIDS grassroots organizations and local Co-Investigators in TZ and KE, both of whom are longstanding collaborators with the investigators' US team and are located in mixed urban and rural areas, allowing examination of effectiveness in two countries and two settings (urban/rural). Using a task-shifting approach, in which lay individuals are trained as counselors, the investigators will train six counselors in each country, who deliver 20 groups in each site (10 rural, 10 urban), resulting in 320 children and adolescents (ages 7-13) who receive TF-CBT and 320 who receive usual care. Outcomes for children are assessed at 12-14 weeks (i.e., corresponding with the end of TF-CBT), 6-months post-treatment, and 12-months post-treatment. TF-CBT experts from the investigators' team partner with the lay counselors from the feasibility study (e.g., local trainers) to train the TZ and KE counselors, and these local trainers provide the TF-CBT supervision, while supervised themselves by the US-based TF-CBT and mental health experts. The investigators expect this trial to yield recommendations regarding an effective intervention for orphans that is acceptable, feasible, and includes local responsibility as a means to enhance potential sustainability in Low- and Middle-Income Countries (LAMICs). Findings will inform other efforts to scale up mental health interventions to address the substantial mental health gap.

Not Provided
Not Provided
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single Blind (Outcomes Assessor)
Primary Purpose: Treatment
  • Childhood Traumatic Grief
  • Post Traumatic Stress
  • Post Traumatic Stress Disorder
  • Depressive Symptoms
  • Behavioral Problems
  • Child Overall Daily Functioning
  • Child and Guardian Relationship
Behavioral: Trauma-focused Cognitive Behavioral Therapy
  • No Intervention: Usual Care Comparison Condition
    Half of the participating children/guardian dyads will receive no intervention (usual care) to serve as a control.
  • Experimental: Trauma-focused CBT group therapy
    Half of the participating children/guardian dyads will receive the 12-week Trauma-focused Cognitive Behavioral Therapy (TF-CBT) group treatment.
    Intervention: Behavioral: Trauma-focused Cognitive Behavioral Therapy
Not Provided

*   Includes publications given by the data provider as well as publications identified by Identifier (NCT Number) in Medline.
Active, not recruiting
December 2017
December 2017   (Final data collection date for primary outcome measure)

Inclusion Criteria:

  • Children ages 7-13 living in Moshi, Tanzania or Bungoma, Kenya who have had one or both parents die since they were 3 years old or older.
  • Children must have scores on study measures indicating they have symptoms of traumatic grief and/or traumatic stress.
  • Children must be living with an adult guardian who is willing to participate in 12 weekly group sessions.
  • Adult guardians of eligible children.

Exclusion Criteria:

  • Living in an institution (not with a guardian).
  • Parent(s) died before child was 3 years old.
Sexes Eligible for Study: All
7 Years to 13 Years   (Child)
Contact information is only displayed when the study is recruiting subjects
United States,   Kenya,   Tanzania
R01MH096633 ( US NIH Grant/Contract Award Number )
Not Provided
Not Provided
Not Provided
Duke University
Duke University
  • National Institute of Mental Health (NIMH)
  • Tanzania Women Research Foundation (TAWREF)
  • Action in the Community Environment (ACE) Africa
Principal Investigator: Shannon Dorsey, PhD University of Washington
Principal Investigator: Kate Whetten, PhD, MPH Duke University
Duke University
November 2016

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP