NCT04004286

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.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
300

participants targeted

Target at P75+ for all trials

Timeline
289mo left

Started Feb 2019

Longer than P75 for all trials

Geographic Reach
1 country

2 active sites

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress23%
Feb 2019Feb 2050

Study Start

First participant enrolled

February 1, 2019

Completed
4 months until next milestone

First Submitted

Initial submission to the registry

June 13, 2019

Completed
19 days until next milestone

First Posted

Study publicly available on registry

July 2, 2019

Completed
30.6 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 1, 2050

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

February 1, 2050

Last Updated

January 28, 2026

Status Verified

January 1, 2026

Enrollment Period

31 years

First QC Date

June 13, 2019

Last Update Submit

January 26, 2026

Conditions

Pain

Keywords

Pain PASTOR Biobank

Outcome Measures

Primary Outcomes (3)

  • 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.

    Up to 30 years

  • Pain Registry: Blood specimens

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

    Up to 30 years

  • Pain Registry: Saliva

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

    Up to 30 years

Eligibility Criteria

Age18 Years - 80 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

Male and female military health care beneficiaries age 18 years and older presenting for an appointment care at WRNMMC

You may qualify if:

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

You may not qualify if:

  • Cannot understand English

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (2)

Naval Medical Center San Diego

San Diego, California, 92134, United States

RECRUITING

Walter Reed National Military Medical Center

Bethesda, Maryland, 20889, United States

RECRUITING

Biospecimen

Retention: SAMPLES WITH DNA

Blood specimens and saliva

MeSH Terms

Conditions

Pain

Condition Hierarchy (Ancestors)

Neurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Officials

  • Harold J Gelfand, MD

    Defense and Veterans Center for Integrative Pain Management

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Mary E McDuffie, RN,BSN

CONTACT

301/400/4242mary.mcduffie.ctr@usuhs.edu

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

June 13, 2019

First Posted

July 2, 2019

Study Start

February 1, 2019

Primary Completion (Estimated)

February 1, 2050

Study Completion (Estimated)

February 1, 2050

Last Updated

January 28, 2026

Record last verified: 2026-01

Locations

US(2)