NCT07746284

Brief Summary

This project seeks to understand inter-individual differences in chronic musculoskeletal pain (cMSKP). Our long-term objective is to develop clinically-feasible decision tools that enable whole-person assessment and management of cMSKP and guide personalized primary, secondary and tertiary prevention strategies. Our secondary objective is to understand how inter-relationships between physiological, biomechanical and psychosocial factors change over time and impact the experience of living with chronic pain.

Trial Health

75
On Track

Trial Health Score

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

Enrollment
200

participants targeted

Target at P75+ for all trials

Timeline
36mo left

Started Mar 2026

Typical duration for all trials

Geographic Reach
1 country

1 active site

Status
enrolling by invitation

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 Progress12%
Mar 2026Aug 2029

Study Start

First participant enrolled

March 13, 2026

Completed
3 months until next milestone

First Submitted

Initial submission to the registry

June 9, 2026

Completed
2 months until next milestone

First Posted

Study publicly available on registry

August 5, 2026

Completed
3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 31, 2029

Expected
1 day until next milestone

Study Completion

Last participant's last visit for all outcomes

August 1, 2029

Last Updated

August 5, 2026

Status Verified

June 1, 2026

Enrollment Period

3.4 years

First QC Date

June 9, 2026

Last Update Submit

July 31, 2026

Conditions

Outcome Measures

Primary Outcomes (1)

  • Symptom network

    We will construct time varying networks for each patient based on longitudinal variables describing multiple domains: psychosocial, biomechanical and physiological. Change in network topology will be used as the primary outcome measure.

    Every 3 months for one year

Secondary Outcomes (3)

  • WOMAC

    Every 3 months for 1 year

  • WHOQOL

    Every 3 months for 1 year

  • Allostatic load

    Every 3 months for 1 year

Study Arms (1)

knee pain group

adults with chronic knee pain

Eligibility Criteria

Age18 Years - 99 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Patients seeking physical therapy

You may qualify if:

  • Adults aged 18-years old or more
  • Chronic pain for 3 months or more around the knee joint.

You may not qualify if:

  • Acute pain due to knee injury or surgery within the past 3 months.
  • Diagnosis of lumbar radiculopathy, neuropathy or neuritis.
  • Special populations i. Adults unable to consent ii. Pregnant women (self-reported) iii. Prisoners iv. George Mason University Athletes
  • Military
  • Bleeding disorders, blood thinners, recent blood transfusions, vasovagal syncope, and current infection.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Optimal Motion Physical Therapy

Herndon, Virginia, 20170, United States

Location

Related Publications (4)

  • Liang Y, Booker C. Allostatic load and chronic pain: a prospective finding from the national survey of midlife development in the United States, 2004-2014. BMC Public Health. 2024 Feb 9;24(1):416. doi: 10.1186/s12889-024-17888-1.

    PMID: 38336697BACKGROUND
  • Borsboom D, Deserno MK, Rhemtulla M, Epskamp S, Fried EI, McNally RJ, et al. Network analysis of multivariate data in psychological science. Nat Rev Methods Primer. 2021 Aug 19;1(1):1-18.

    BACKGROUND
  • Fillingim RB. Individual differences in pain: understanding the mosaic that makes pain personal. Pain. 2017 Apr;158 Suppl 1(Suppl 1):S11-S18. doi: 10.1097/j.pain.0000000000000775.

    PMID: 27902569BACKGROUND
  • McBeth J, Jones K. Epidemiology of chronic musculoskeletal pain. Best Pract Res Clin Rheumatol. 2007 Jun;21(3):403-25. doi: 10.1016/j.berh.2007.03.003.

    PMID: 17602991BACKGROUND

Biospecimen

Retention: SAMPLES WITHOUT DNA

Serum

Study Design

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

Study Record Dates

First Submitted

June 9, 2026

First Posted

August 5, 2026

Study Start

March 13, 2026

Primary Completion (Estimated)

July 31, 2029

Study Completion (Estimated)

August 1, 2029

Last Updated

August 5, 2026

Record last verified: 2026-06

Data Sharing

IPD Sharing
Will share

Deidentified records including patient reported outcomes will be shared.

Time Frame
After publication of primary study results

Locations