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

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

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04004286
Acronym
PRBiobank
Enrollment
300
Registered
2019-07-02
Start date
2019-02-01
Completion date
2050-02-01
Last updated
2026-01-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pain

Keywords

Pain PASTOR Biobank

Brief summary

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.

Detailed description

The Defense and Veterans Center for Integrative Pain Management (DVCIPM) established a clinical data registry and tissue biobank (pain registry/biobank) for the advancement of pain-related research. This Pain Registry Biobank will address the complexity of pain by utilizing the Pain Assessment Screening Tool & Outcomes Registry (PASTOR), a thorough biopsychosocial assessment 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. As a uniform assessment system, PASTOR also mitigates a significant challenge in pain-related research, the lack of standardized, cross-study outcomes. Additionally, the richness of PASTOR data matched with biological samples allows future researchers to address significant research gaps and enhance health care for service members, veterans, and civilians.

Interventions

None listed

Sponsors

Defense and Veterans Center for Integrative Pain Management
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
Yes

Inclusion criteria

* Eligibile for care within the Military Healthcare System * Able and willing to provide written consent

Exclusion criteria

* Cannot understand English

Design outcomes

Primary

MeasureTime frameDescription
Pain Registry: PASTOR surveyUp to 30 yearsa 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 specimensUp to 30 years43 ml of blood collected and processed for storage from EDTA, BDP 100, PAXgene RNA, and DNA blood collection tubes
Pain Registry: SalivaUp to 30 yearsup to 10ml of saliva, collected in 2ml cryovials.

Countries

United States

Contacts

CONTACTMary E McDuffie, RN,BSN
mary.mcduffie.ctr@usuhs.edu301/400/4242
PRINCIPAL_INVESTIGATORHarold J Gelfand, MD

Defense and Veterans Center for Integrative Pain Management

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026