Recruiting

Observational Study

Sponsor:

UCLA

Code:

NCT06605014

Conditions

Stroke, Acute

TIA

Reproducibility of Results

Osteopathic Manipulation

Health-Related Quality-of-Life

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Accepted

Study Details

Brief summary:

The goals of this observational study are to test the reliability of a new, standardized physical examination method to identify motion problems within joints or groups of joints among adult asymptomatic volunteers and in patients hospitalized with stroke or stroke-like episodes (e.g., transient ischemic attack, TIA). The main questions this investigation aims to answer are:

  • Can different, independent providers reliability quantify motion pattern problems using a systematic approach called, The Functional Pathology of the Musculoskeletal System (FPMSS) model?
  • Are there differences in joint(s) motion patterns among asymptomatic volunteers, patients with TIA (people with brain disease without new neurologic disability), and recent ischemic stroke (patients with new stroke-related-disability, e.g., paralysis)?
  • Is there an association between joint(s) motion impairment severity and stroke survivor outcomes?

Participants (asymptomatic and those with stroke) will undergo a set of repeated paired, musculoskeletal physical exams by independent providers blinded to each other's assessments and patient information. Researchers will compare the severity, location, and quantity of joint(s) motion impairment between these three groups with the physical examination methodology (FPMSS). Clinical information (e.g., test results, diagnoses, brain imaging, medical history) will be collected from patients admitted for TIA and stroke. Enrolled participants with recent stroke will complete a survey three months after hospitalization to determine their self-perceived quality-of-life.

Conditions

Stroke, Acute

TIA

Reproducibility of Results

Osteopathic Manipulation

Health-Related Quality-of-Life

Study ID

NCT06605014

Start date

Sep 1, 2023

Status verified date

Sep, 2025

Completion date

Aug 31, 2026

Anticipated

Primary completion date

Jun 30, 2026

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Accepted

Inclusion Criteria:

  • adults ≥18 years

Admission diagnosis:

  • ischemic stroke OR
  • transient ischemic attack (TIA). A prior history of TIA but without stroke may be enrolled.
  • Neurologic stability or lack of significant deterioration (i.e. ∆ NIHSS<4) for at least 24 hours (defined by clinical documentation and/or communication with provider team(s)) in stroke subjects
  • Able to sit upright, lie supine, and when able lateral recumbent left/right positions with assist independently or with minimal person assist
  • Anticipated length of stay greater > or = 2 days for ischemic stroke. TIA patients average length of stay is < 2 days, and can be enrolled in the study.

Exclusion Criteria:

  • Acute skeletal fracture or known dislocation; history of pathologic (osteoporotic or neoplastic) skeletal fracture of thoracic cage, hip/pelvis/sacrum, or vertebral column
  • Prior history of ICH, ischemic stroke, confirmed by imaging and/or clinical evaluation. Patients with imaging showing "chronic stroke" who have never received a diagnosis of stroke and/or have not been previously symptomatic may still be enrolled, based on the Investigator's clinical judgement.
  • Spinal column support brace (e.g. cervical collar)
  • Anticipated neurosurgical intervention during hospitalization: decompressive hemicraniectomy, hematoma evacuation (defined by clinical documentation and/or communication with provider team(s))
  • Current endotracheal intubation (\*note: extubated patients can be evaluated for eligibility)
  • History of spinal cord injury with residual neuromuscular or sensory disability
  • History of recent trauma within the past 30 days
  • Known ligament, musculotendinous, or bone lesion
  • Clinical condition that would interfere with execution of movement or palpatory diagnostic testing, e.g. chronic pain
  • History of spinal surgery

Study Design

Enrollment

120 participants

Anticipated

Interventions and Outcome Measures

Arms

SOMADC-AC Cohort

1. Asymptomatic adult volunteers
2. Patients admitted with TIA
3. Patients admitted with acute ischemic stroke

Primary outcome measure

  • Examiner Rater-Reliability [ Time Frame: 3 to 14 days ]
  • Functional Pathology of the Musculoskeletal System [ Time Frame: 3-14 days ]
  • National Institutes of Health Neuro-Quality of Life (QoL) survey [ Time Frame: 90 days ]

Central Contacts and Locations

Central contacts

Locations

University of California Davis Medical Center

Recruiting

Sacramento, California, United States, 95817

Principal Investigator:

Alan Yee, D.O.

More Information

Sponsor

University of California, Davis

Last update posted

Sep 26, 2025

Last verified

Sep, 2025

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by University of California, Davis on 2025-09-26.