Actively Recruiting
Sociocultural & Biobehavioral Influences on Pain Expression and Assessment
Led by National Center for Complementary and Integrative Health (NCCIH) · Updated on 2026-04-24
700
Participants Needed
1
Research Sites
472 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Objective The current proposal investigates behavioral, psychophysiological, and social processes that may help explain biases and disparate outcomes in pain. Health disparities, or health outcomes that adversely affect disadvantaged populations, are pervasive and apparent in many diseases and symptoms, including pain. Pain is the number one reason individuals seek medical treatment. Health disparities in pain encompass both differences in pain experience and treatment for pain. For instance, research indicates that Black individuals report increased pain and have reduced pain tolerance relative to White individuals, yet doctors are less likely to treat minority patients pain and underestimate their pain experience. This project aims to address this systemic discrepancy by focusing on interpersonal processes that may contribute to these disparities, including socially-relevant responses to pain (i.e. pain expression) and pain assessment (e.g. visual attention). The proposed research aims to determine whether the study of pain expressions and their assessment can yield insights on how social factors shape pain and its treatment. Further, we test the efficacy of potential interventions designed to improve accuracy and reduce biases in pain assessment. If successful, this work will form the foundation of a new research program that will link the field of pain research with the field of social neuroscience, and forge new insights on the critical problem of health disparities in pain. Study population We will accrue up to 700 total healthy volunteers to target 240 completers Design Our overall aim is to understand how social factors influence the assessment and management of pain, and to gain insight into psychosocial processes that may underlie health disparities in pain. We propose a series of studies designed to test these links. First, we will measure pain perception and physiological responses to painful stimuli in a diverse group of individuals to test for sociocultural and biological influences on pain and pain-related responses. In subsequent studies, new participants ("perceivers") will view images of these initial participants ("targets") and will provide estimates of 'targets' pain experience. We will measure a) whether perceivers can accurately estimate 'targets' pain experience; b) whether accuracy differs as a function of similarity between target and perceiver (ingroup vs outgroup); and c) whether individuals can improve accuracy through feedback. Outcome measures Primary outcome measures for all experiments will be decisions about pain (experienced by self or other) measured with visual analogue scales, reaction time, and/or categorical judgments (pain/no pain). We will also measure physiological responses (e.g., facial muscle response, skin conductance, pupil dilation) and brain responses using functional magnetic resonance imaging (fMRI) as secondary outcome measures. We will test whether pain and pain-related responses varies as a function of sociocultural/demographic factors (e.g. race, ethnicity, sex) and whether accuracy in assessing others' pain is influenced by group similarity (i.e. ingroup vs. outgroup) and training (e.g. performance-related feedback)....
CONDITIONS
Official Title
Sociocultural & Biobehavioral Influences on Pain Expression and Assessment
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Healthy
- Between 18 and 60 years old
- Fluent in English
- Able to provide written informed consent
You will not qualify if you...
- Unable to comply with study procedures
- Major medical condition or history affecting compliance, including neurological issues (stroke, blindness, deafness, brain damage)
- Current mood, anxiety, substance use disorder, history of psychosis, psychiatric hospitalization, or recurrent psychiatric episodes
- NIH staff member subordinate, relative, or co-worker of protocol investigators
- Prior participation in a different sub-study within this protocol
- Born outside the United States or its territories
- Does not currently reside in the United States or its territories
- For sub-study 1: medical conditions affecting heat sensitivity or pain thresholds (e.g., cardiovascular, autonomic, neurological, diabetes)
- Medical conditions affecting somatosensation (e.g., Raynaud's disease, peripheral neuropathy, circulatory disorders)
- Current or past chronic pain lasting more than six months
- Dermatological issues in testing areas (scars, burns, recent tattoos)
- Regular use of prescription medications significantly affecting pain or heat perception (certain opiates, antidepressants, anticonvulsants, anxiolytics, hypnotics, antipsychotics, antimigraine agents, muscle relaxants)
- Left-handedness
- For sub-study 4 (fMRI participants): left-handedness, chronic pain history, fMRI contraindications (ferromagnetic implants, pacemakers, insulin pumps, irremovable piercings), pregnancy, structural MRI abnormalities with functional consequences
AI-Screening
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Trial Site Locations
Total: 1 location
1
National Institutes of Health Clinical Center
Bethesda, Maryland, United States, 20892
Actively Recruiting
Research Team
A
Adebisi O Ayodele, C.R.N.P.
CONTACT
L
Lauren Y Atlas, Ph.D.
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NON_RANDOMIZED
Model
SEQUENTIAL
Primary Purpose
BASIC_SCIENCE
Number of Arms
4
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