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Pain Screening in Refugee Survivors of Torture

The Implementation of a Novel Pain-screening Tool in the Diagnoses of Pain Symptoms and Syndromes in Refugee Survivors of Torture

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03018782
Enrollment
25
Registered
2017-01-12
Start date
2017-01-31
Completion date
2019-06-21
Last updated
2021-07-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pain, Chronic

Brief 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.

Detailed 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.

Interventions

OTHERBrief Pain Inventory Short Form

Brief Pain Inventory Short Form

Sponsors

Weill Medical College of Cornell University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 100 Years
Healthy volunteers
No

Inclusion criteria

* Men and women from any country over the age of 18 * refugees receiving services from the Weill Cornell Center for Human Rights

Exclusion criteria

* Have not experienced torture * Subjects whose representative does not believe that they are a good candidate for the study

Design outcomes

Primary

MeasureTime frameDescription
Number of participants with chronic pain or pain syndromes as assessed by a non-invasive pain evaluation conducted by a pain physicianDay 1Evaluate whether or not current standard protocols for the assessment of survivors of torture result in under or missed diagnosis of pain and pain syndromes that are identifiable by a pain specialist physician

Secondary

MeasureTime frameDescription
Number of participants with chronic pain or pain syndromes as assessed by the Brief Pain Inventory (BPI) Short FormDay 1Evaluate whether or not a validated pain screening tool can supplement the current standard protocols used in the assessment of survivors of torture.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 18, 2026