Cardiovascular, Cerebrovascular, and Cognitive Function in Spinal Cord Injury

NCT ID: NCT02122991

Last Updated: 2018-02-19

Basic Information

• Recruitment Status: COMPLETED
• Total Enrollment: 61 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2013-07-31
• Study Completion Date: 2017-12-31

Brief Summary

Increased life expectancy in individuals with spinal cord injury (SCI) present clinicians with the challenge of managing the secondary complications of SCI with the chronic diseases common in an aging population. Cardiovascular disease, cerebral vascular disease, and cognitive dysfunction are among the primary challenges facing clinicians in the treatment of an aging population. Cognitive dysfunction has been reported in upwards of 60% of the SCI population, which have been primarily attributed to concomitant traumatic brain injury or pre-morbid conditions. Identifying possible modifiable risk factors which contribute to the increased prevalence of cognitive dysfunction in the SCI population is of significant clinical relevance and cardiovascular and cerebrovascular disorders have emerged as possible contributors to the cognitive disorders in the general population. These risk factors include: physical inactivity, chronically low or high blood pressure (BP), reduced blood flow to the brain, arterial stiffening, and impaired nervous system regulation of the cardiovascular system. These risk factors are particularly prominent in the SCI population as they represent a model of profound inactivity, have trouble regulating blood pressure, and suffer impaired cardiovascular regulation from their injury. In addition, we've recently reported deficits in blood flow to the brain at rest and during cognitive tests; with results being further impaired in SCI with chronically low blood pressure. Therefore the goals of this project are to determine the influence of cardiovascular and cerebral vascular responses at rest and during cognitive testing on test performance in 80 individuals with SCI compared to 50 age-matched non-SCI controls. All potential subjects will undergo a rigorous two-part screening process which consists of an initial screening via telephone and a detailed, in-person screening. Eligible subjects will be invited to participate in a 3 hour laboratory visit during which their arterial stiffness, blood pressure, heart rate, respiration rate and, blood flow to the brain will be monitored at rest and during a comprehensive series of cognitive tests.

We hypothesize that blood pressure and cerebrovascular response to testing will account significantly for performance in cognitive testing that otherwise would have been attributable to SCI status.

Detailed Description

The cognitive test battery will consists of the tests listed below, administered in the order given. Each test will be scored according to the

1. California Verbal Learning Test (Total & SD?)

2. Controlled oral word association test

3. Symbol Digit Modalities Test (Oral version)

4. Trail Making Test (Oral version)

5. Stroop Test (W?, C?, CW?)

6. Digit Span (Forwards, Backwards, and Sequencing)

7. California Verbal Learning Test (LD? & Recognition?)

8. Letter-Number Sequencing

9. California Verbal Learning Test (LD Forced recognition?)

10. WASI-II Sub-tests (Vocabulary, Similarities, and Matrix Reasoning)

Conditions

Spinal Cord Injury

Study Design

• Observational Model Type: CASE_CONTROL
• Study Time Perspective: CROSS_SECTIONAL

Study Groups

Able-Bodied Controls

Subjects must be between the ages of 30 and 64 years old, be English-literate and able to provide informed consent. They must score at least 20/60 minimum acuity in their worst eye on the Snell Eye Exam, and score at least 22 on the Montreal Cognitive Assessment. Subjects MUST NOT HAVE: an acute illness or infection, history of stroke, recent illicit drug abuse (\<6 months), unstable/uncontrolled seizures, neurodegenerative disease, Severe Traumatic Brain Injury (as determined by TBI screening tool), any significant history of neurological disease/disorder, any significant systemic illness or unstable medical condition (uncontrolled diabetes, hypo- or hyperthyroidism, systemic cancer), history of schizophrenia or bipolar disorder or any active psychosis, or alcohol/substance abuse or dependence (\<6 months).

No interventions assigned to this group

Spinal Cord Injury

Subjects must be between the age of 30 and 64 years old, be English-literate and able to provide informed consent. They must be at least 1 year from the date of their spinal cord injury. They must score at least 20/60 minimum acuity in their worst eye on the Snell Eye Exam, and score at least 22 on the Montreal Cognitive Assessment. Subjects MUST NOT HAVE: an acute illness or infection, history of stroke, recent illicit drug abuse (\<6 months), unstable/uncontrolled seizures, neurodegenerative disease, Severe Traumatic Brain Injury (as determined by TBI screening tool), any significant history of neurological disease/disorder, any significant systemic illness or unstable medical condition (uncontrolled diabetes, hypo- or hyperthyroidism, systemic cancer), history of schizophrenia or bipolar disorder or any active psychosis, or alcohol/substance abuse or dependence (\<6 months).

No interventions assigned to this group

Eligibility Criteria

Inclusion Criteria

• Between the ages of 30 and 64 years old
• If SCI, the duration of injury must be greater than 1 year
• At least 20/60 minimum acuity in worst eye on the Snell Eye Exam
• A score ≥22 on the Montreal Cognitive Assessment
• English literate
• Able to provide informed consent

Exclusion Criteria

• Acute illness or infection
• Documented history of:

• Stroke
• Recent illicit drug abuse (from medical chart, within the past 6-months)
• Unstable or uncontrolled seizures
• Neurodegenerative disease including Alzheimer's disease, Parkinson's disease, Huntington's disease
• Severe TBI (identified by TBI screening tool)
• Any significant history of neurological disease/disorders:

• Alzheimer's disease
• Parkinson's disease
• Vascular dementia
• Huntington's disease
• Pick's disease
• Lewy Body Dementia
• Frontotemporal dementia
• Normal pressure hydrocephalus
• Brain tumor
• Progressive supranuclear palsy
• Seizure disorder
• Multiple sclerosis
• Any significant systemic illness or unstable medical condition, including:

• Uncontrolled diabetes mellitus,
• Uncorrected hypothyroidism or hyperthyroidism,
• Systemic cancer.
• History of schizophrenia or bipolar disorder or any active psychosis
• Alcohol or substance abuse or dependence within the past 6 months (from medical record)

• Minimum Eligible Age: 30 Years
• Maximum Eligible Age: 64 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

James J. Peters Veterans Affairs Medical Center

FED

Sponsor Role: lead

Responsible Party

Jill M. Wecht, Ed.D.

Research Health Scientist

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Jill M Wecht, Ed.D.

Role: PRINCIPAL_INVESTIGATOR

JJPVAMC

Locations

James J Peters VA Medical Center

The Bronx, New York, United States

Countries

United States

Other Identifiers

01492

Identifier Type: OTHER

Identifier Source: secondary_id

WEC-13-024

Identifier Type: -

Identifier Source: org_study_id