About this trial
This Pain Registry Biobank is a prospective cohort design study whereby data (PASTOR survey, blood and saliva specimens, clinical data) is collected from participants in a longitudinal fashion with continual enrollment.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Eligibile for care within the Military Healthcare System
Able and willing to provide written consent
Disqualifiers
Cannot understand English
Trial population
Male and female military health care beneficiaries age 18 years and older presenting for an appointment care at WRNMMC
Trial design
Other
Prospective
Treatments tested in this trial
Not listed
Trial groups
Trial outcomes
Primary outcomes
Pain Registry: PASTOR survey
a thorough biopsychosocial assessment computer adaptive screening tool that extends beyond a single-item pain rating scale. PASTOR is an assessment battery that includes several Patient Reported Outcomes Measurement Information System (PROMIS) scales developed by the National Institutes of Health (NIH) and other important scales that span physical, psychological, social, and behavioral aspects of pain and pain-related treatments.
Pain Registry: Blood specimens
43 ml of blood collected and processed for storage from EDTA, BDP 100, PAXgene RNA, and DNA blood collection tubes
Pain Registry: Saliva
up to 10ml of saliva, collected in 2ml cryovials.
Sponsors and contacts
Click on the lead sponsor to view all of their trials.