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Controlled Trial of Mental Health Interventions for Torture Survivors in Kurdistan

Johns Hopkins Bloomberg School of Public Health logo

Johns Hopkins Bloomberg School of Public Health

Status

Completed

Conditions

Depression

Treatments

Behavioral: Behavioral Activation
Behavioral: Cognitive Processing Therapy
Behavioral: nonspecific counseling

Study type

Interventional

Funder types

Other

Identifiers

NCT00925262
BoltonP-1

Details and patient eligibility

About

The purpose of this study is to determine the relative effectiveness of three different mental health counseling interventions in the treatment of mental health problems commonly affecting torture and trauma survivors living in Kurdistan, Iraq.

Full description

See above

Enrollment

530 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • at least 18 years old
  • Kurdish
  • torture survivor
  • currently has significant depression symptomatology.

Exclusion criteria

  • danger to self or others
  • already receiving treatment from our treatment provider
  • not mentally competent to provide informed consent.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

530 participants in 4 patient groups

Cognitive Processing Therapy
Experimental group
Description:
An adaptation of cognitive behavioral therapy, focusing on treatment for persons suffering mental health effects of trauma
Treatment:
Behavioral: Cognitive Processing Therapy
Behavioral Activation
Experimental group
Description:
A form of counseling therapy that emphasizes enhancing pleasurable behaviors and minimizing negative behaviors as a means to reducing depression symptomatology.
Treatment:
Behavioral: Behavioral Activation
non-specific counseling
Experimental group
Description:
a collection of counseling skills suitable for a broad range of mental health and psychosocial problems and not designed for specific disorders. This particular version was developed by a collaborator -Heartland Alliance - for use with torture survivors.
Treatment:
Behavioral: nonspecific counseling
wait control
No Intervention group
Description:
persons in this study arm will not receive active treatment as part of the study but will be monitored during the study and offered treatment after 3-5 months of waiting.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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