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Clinical Trial Summary

The investigators are evaluating refugee torture survivors who are receiving services at the Weill Cornell Center for Human Rights. There are two research questions in this study: if the current standard of care results in the under or missed diagnosis of pain and pain syndromes, and if a validated pain screening tool can supplement the current standard protocol used in the assessments of survivors of torture.


Clinical Trial Description

The research plan consists of three components: 1. The Weill Cornell Center for Human Rights will coordinate with the research team regarding eligible subjects. 2. Researchers will contact potential subjects utilizing interpreter services. 3. Interested participants will be scheduled for an appointment for an examination by a pain physician and to complete the Brief Pain Inventory. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03018782
Study type Interventional
Source Weill Medical College of Cornell University
Contact
Status Completed
Phase N/A
Start date January 2017
Completion date June 21, 2019

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