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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00925262
Other study ID # BoltonP-1
Secondary ID
Status Completed
Phase N/A
First received June 3, 2009
Last updated May 1, 2013
Start date June 2009
Est. completion date October 2011

Study information

Verified date May 2013
Source Johns Hopkins Bloomberg School of Public Health
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

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.


Description:

See above


Recruitment information / eligibility

Status Completed
Enrollment 530
Est. completion date October 2011
Est. primary completion date February 2010
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility 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.

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Behavioral:
Cognitive Processing Therapy
an adaptation of cognitive behavioral therapy used to address mental health effects of trauma exposure
Behavioral Activation
form of counseling intervention to promote positive behaviors and reduce negative behaviors as a means of reducing depression symptomatology and severity
nonspecific counseling
nonspecific counseling interventions useful for a broad range of mental health and psychosocial problems.

Locations

Country Name City State
Iraq multiple public health clinics across Kurdistan Dohuk, Sulaimani, Erbil, rural areas ALL

Sponsors (1)

Lead Sponsor Collaborator
Johns Hopkins Bloomberg School of Public Health

Country where clinical trial is conducted

Iraq, 

Outcome

Type Measure Description Time frame Safety issue
Primary depression symptom severity 3-6 months No
Secondary ability to carry out routine tasks and activities 3-6 months No
Secondary anxiety symptom severity 3-6 months No
Secondary posttraumatic stress disorder symptom severity 3-6 months No
Secondary traumatic grief symptom severity 3-6 months No
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