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RecruitingNCT02994121PROMOTEUpdated Dec 29, 2025

Prospective Investigation of Multiple Sclerosis in the Three Rivers Region

An observational study in Multiple Sclerosis, sponsored by University of Pittsburgh. Recruiting at 1 site in United States. Open to participants aged 7 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2025-12-29.

Sponsored by University of Pittsburgh · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
7,500
Ages
7 Years and older
Sex
All
01

Study summary

In this longitudinal prospective natural history study of multiple sclerosis (MS), the overarching goal is to understand the factors that influence individual variation in disease trajectory and treatment response and pave the way for realizing precision medicine in MS. Because MS is a chronic neurological disorder, this observational cohort study will span a 30-year time frame.

Read the detailed description

Research Activities: Initial Questionnaire, Questionnaire for Self-Reported Outcomes, Biological Sample Collection (Blood, Stool, Urine, Cerebrospinal fluid), Genetic Analysis, Standard Quantitative Assessment of Function, Cognitive Assessment, Neuroimaging, Biometric Sensors, Social Network Questionnaire, Connor-Davidson Resilience Scale, NEO Five-Factor Inventory, and the COVID19 Response Surveys.

02

Conditions studied

  • Multiple Sclerosis

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03

In context

Multiple Sclerosis

3,460 studies on the registry are indexed under Multiple Sclerosis; 661 are open to participants now.

This study's planned enrollment of 7,500 is above the median of 100 across 1,016 observational studies indexed under Multiple Sclerosis.

Browse Multiple Sclerosis studies →

Lead sponsor

University of Pittsburgh is the lead sponsor of 1,385 studies on the registry; 167 are open to participants now.

Of its 8 completed or terminated interventional studies of FDA-regulated products, 4 (50%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
7 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

People with multiple sclerosis and related disorders and controls

Eligibility criteria

Inclusion Criteria:

  • Inclusion criteria for MS patients include:

    1. Age 7 years or older
    2. Willing and able to provide consent (for >=18 years) or assent with permission from at least one of the child's parents (for \<18 years)
    3. Diagnosis of multiple sclerosis or related disorders, including a first central nervous system demyelinating episode with a positive MRI scan or abnormal MRI scans characteristic of MS but no clinical symptoms of the disease
  • For healthy controls:

    1. Age 7 years or older
    2. Willing and able to provide consent (for >=18 years) or assent with permission from at least one of the child's parents (for \<18 years)
    3. No known personal history of multiple sclerosis or related disorders
    4. No other chronic diseases
    5. Family members, unrelated household controls, or controls from the general population could be eligible

There is no exclusion criteria.

05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
7,500 participants (estimated)
Patient registry
No
Biospecimen retention
Samples with dna

Groups and cohorts

  • People with Multiple Sclerosis or Related Disorders

    Individuals must be 7 years or older, diagnosed with multiple sclerosis or related disorders, including a first central nervous system demyelinating episode with a positive MRI scan or abnormal MRI scans characteristic of MS but no clinical symptoms of the disease

  • People without Multiple Sclerosis or Related Disorders

    Control participants must be 7 years or older, have no known personal history of multiple sclerosis or related disorders, no other chronic disease, and can be a family member, unrelated household control, or control from the general population.

06

What researchers measure

Primary outcomes

  1. Establish a prospective cohort of well-characterized MS patients and controls

    For this longitudinal prospective observational study, we will establish a prospective cohort of well-characterized MS patients and controls (2:1).

    Time frame: within 30 years

  2. Investigate the predictors of the variations in disease trajectory and treatment response

    Understanding the factors that influence disease trajectory and treatment response will pave the way to realize precision medicine in delivering individualized MS care.

    Time frame: within 30 years

07

Study locations

1 of 1 sites recruiting
  • University of Pittsburgh
    Pittsburgh, Pennsylvania 15260, United States
    • Zongqi Xia, MD, PhD · Contact · 412-383-5377
    Recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 29, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT02994121
Lead sponsor
University of Pittsburgh
Responsible party
Zongqi Xia (MD, PhD, University of Pittsburgh) — Principal investigator
First posted
Dec 15, 2016
Start date
Dec 2016
Primary completion
Jan 2047 (estimated)
Completion
Jan 2047 (estimated)
Last update
Dec 29, 2025

Study contacts

Zongqi Xia, MD, PhD
Contact
msstudy2@pitt.edu
412-383-5377
Zongqi Xia, MD, PhD
principal investigator · University of Pittsburgh

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

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