NCT07714044

Brief Summary

The goal of this study is to enroll at least 10,000 participants nationally including affecteds and unaffecteds via online study portal, collect surveys online and a saliva sample through the mail, sequence DNA, and conduct genetic analyses to identify novel variants and further study known variants associated with leukemia, lymphoma, myeloma and other blood cancers.

Trial Health

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Monitor

Trial Health Score

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

Enrollment
10,000

participants targeted

Target at P75+ for all trials

Timeline
37mo left

Started Aug 2026

Typical duration for all trials

Geographic Reach
1 country

1 active site

Status
not yet 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

First Submitted

Initial submission to the registry

July 15, 2026

Completed
5 days until next milestone

First Posted

Study publicly available on registry

July 20, 2026

Completed
12 days until next milestone

Study Start

First participant enrolled

August 1, 2026

Completed
3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 1, 2029

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

August 1, 2029

Last Updated

July 20, 2026

Status Verified

July 1, 2026

Enrollment Period

3 years

First QC Date

July 15, 2026

Last Update Submit

July 15, 2026

Conditions

Keywords

geneticsblood cancerblood cancersleukemialymphomamyelomahematologic cancerhematologic malignancyhematologic tumorhematologic neoplasm

Outcome Measures

Primary Outcomes (1)

  • Genetic risk variants associated with blood cancer

    Genetic factors will be measured through whole exome sequencing and genome-wide genotyping array, and then correlated with blood cancer subtype.

    2 years

Study Arms (2)

Cases

Persons with blood cancer

Controls

Persons who do not have blood cancer

Eligibility Criteria

Age18 Years - 110 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

The study population consists of anyone at least 18 years old who lives in the United States, including both individuals who have or had blood cancer and those who have not. Participants include males, females, non-binary, and all race-ethnic groups.

You may qualify if:

  • age 18 years or older
  • currently living in the United States
  • have access to the internet and a computer, laptop, tablet or smartphone
  • willing to provide written informed consent for participation
  • willing to provide DNA via a saliva sample using a collection kit mailed to your home
  • willing to complete a survey with questions about health related to the study of blood cancer.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Rutgers University

Piscataway, New Jersey, 08854, United States

Location

Biospecimen

Retention: SAMPLES WITH DNA

Saliva sample

MeSH Terms

Conditions

Hematologic NeoplasmsLeukemiaLymphomaNeoplasms, Plasma Cell

Condition Hierarchy (Ancestors)

Neoplasms by SiteNeoplasmsHematologic DiseasesHemic and Lymphatic DiseasesNeoplasms by Histologic TypeLymphoproliferative DisordersLymphatic DiseasesImmunoproliferative DisordersImmune System Diseases

Study Officials

  • Tara Matise, PhD

    Rutgers University

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Tara Matise, PhD

CONTACT

Study Design

Study Type
observational
Observational Model
CASE CONTROL
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Distinguished Professor

Study Record Dates

First Submitted

July 15, 2026

First Posted

July 20, 2026

Study Start

August 1, 2026

Primary Completion (Estimated)

August 1, 2029

Study Completion (Estimated)

August 1, 2029

Last Updated

July 20, 2026

Record last verified: 2026-07

Data Sharing

IPD Sharing
Will not share

Our study protocol does not include sharing IPD.

Locations