CHPS RESEARCH STUDIES

Reliability and Validity of Bedside Pain Sensitivity Testing Protocols

The primary purpose of this research study is to determine the reliability of bedside quantitative sensory testing (QST) measures and validity when compared to laboratory QST measures. QST involves several different measurements of how a person perceives pain, including pain threshold and pain sensitivity testing.

During one session that lasts 2.5 hours, you will complete a few simple measures of pain. You will be briefly exposed to heat, cold, pinprick, and pressure to examine your pain threshold and sensitivity. You will also complete questionnaires that characterize your thoughts and feelings about pain.

Inclusion Qualifications:

Be 18-35 years old
Currently pain free
English speaking

Exclusion Qualifications:

You may not participate in this research opportunity if any of the following applies to you:

Regular use of prescription pain medication
History of a chronic pain condition, such as fibromyalgia
Medical conditions that affect sensation, such as uncontrolled diabetes
Any blood clotting disorders, such as hemophilia
Any condition that would prevent you from direct exposure to ice or icy water, such as:
- Uncontrolled hypertension (blood pressure over 140/90 mmHg)
- Cryoglobulinemia (condition in which you have abnormal protein in the blood causing the blood to become thick when exposed to cold)
- Paroxysmal cold hemoglobinuria (autoimmune condition causing the destruction of blood cells after cold exposure)
- Circulatory compromise (blood that does not flow to your arms and legs correctly)
- Open wound on hand
Exceed safety threshold for pressure testing
Currently pregnant

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