| A Special Thank You to Our Research Participants |
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The research team of the Psychophysiology Laboratory for Affective Neuroscience (PLAN) would like to extend their appreciation to the hundreds of women and men who have participated in research at PLAN. Without their selfless contributions it would be impossible for us to further the science of pain and emotion. Please visit the “Publications” page to read our published research. |
| Sensory Processing In Chronic Pain |
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Chronic pain affects millions nationwide and can be quite debilitating for those afflicted. Research currently conducted in our laboratory is aimed at understanding the mechanisms that contribute to the onset and maintenance of chronic pain. This work may ultimately suggest more effective treatment for pain and its management. This study assesses individuals who have a documented diagnosis of Fibromyalgia or Rheumatoid Arthritis. Individuals are also needed who have a verified diagnosis of Primary Insomnia or Major Depressive Disorder. Determination of eligibility will be evaluated by a brief phone screening. Eligible individuals will participate in a laboratory physiological assessment. This study is safe and non-invasive and only requires 5.5 hours to participate. Compensation is provided for participants who complete the study. |
| Participants: |
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Must be at least 18 years of age and have been given a diagnosis of Fibromyalgia, Rheumatoid Arthritis, Primary Insomnia, OR Major Depressive Disorder. |
| Contact: |
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To obtain more information regarding this study, contact Jennifer DelVentura, B.S.,by email or at 918-631-2175; 631-3565. |
| Development of an Objective Marker of Physiological Pain Responding |
| The purpose of this study is to develop an objective measure of pain responding. To do so, several electric stimuli will be delivered to the ankle and several physiological and subjective reactions to these stimuli will be recorded. This research will contribute to the development of a standardized methodology to assess pain responding and may ultimately provide methods for assessing persons at risk for developing chronic pain. This study takes approximately 2˝ hours to complete. Compensation is provided for participation. |
| Participants: |
| Must be at least 18 years of age, in good health, and have no history of cardiac disorders, neurological, neuromuscular disorders, or chronic pain. |
| Contact: |
| To obtain more information regarding this study, contact Ellen Terry, B.A.,by email or at 918-631-2175; 631-3565. |
| The Effects of the Menstrual Cycle and Premenstrual Symptoms on Pain Regulation |
| The principal intention of this study is to investigate physiological and behavioral reactions to electric stimulations and ischemic pain across different phases of the menstrual cycle in females with Premenstrual Dysphoric Disorder (PMDD), as well as healthy females. Participants are required to attend three laboratory sessions and monitor their menstrual cycles daily, for a total of three cycles. Eligibility for participation will be determined by a brief phone health status screening. This study is safe and non-invasive and compensation is provided. |
| Participants: |
| Female participants must be at least 18 years of age, have regular menstrual cycles, have not taken hormone preparations (ie., birth control) or been pregnant within the past 6 months, currently in good health, and have no present symptoms of chronic pain. |
| Contact: |
| To obtain more information regarding this study, contact Emily Bartley M.S.,by email or at 918-631-2175; 631-3565. |
| Current Participants, Click Here |