Defense and Veterans Center for Integrative Pain Management (DVCIPM) Pain Registry Biobank

ConditionPain
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-80
SponsorDefense and Veterans Center for Integrative Pain Management

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 volunteers

Qualifiers

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

Design model

Other

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

No trial groups listed

Trial outcomes

Primary outcomes

1

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.

Time frame
Up to 30 years
2

Pain Registry: Blood specimens

43 ml of blood collected and processed for storage from EDTA, BDP 100, PAXgene RNA, and DNA blood collection tubes

Time frame
Up to 30 years
3

Pain Registry: Saliva

up to 10ml of saliva, collected in 2ml cryovials.

Time frame
Up to 30 years

Secondary outcomes

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.