Effect of Lifestyle Changes on BDNF Level After Stroke

NCT ID: NCT03701815

Last Updated: 2018-10-10

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: NA
• Total Enrollment: 12 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2018-01-19
• Study Completion Date: 2019-02-28

Brief Summary

This is a pilot study to determine whether a lifestyle medicine intervention following stroke may increase levels of Brain-Derived Neurotrophic Factor (BDNF).

Detailed Description

This is a substudy of the study entitled "Assessing a Multi-Disciplinary Lifestyle Medicine Intervention Following Stroke," specifically looking at the effects of lifestyle change on brain-derived neurotrophic factor (BDNF). BDNF has emerged as a key facilitator of neuroplasticity to improve motor learning and rehabilitation after stroke. Aerobic exercise has been shown to increase levels of BDNF in multiple parts of the central nervous system and therefore may facilitate neuroplasticity and motor recovery. While BDNF levels appear to be increased for up to 1 hour following a bout of aerobic exercise, it is unclear whether regular aerobic exercise over weeks to months can increase baseline BDNF levels in humans following stroke.

An single nucleotide polymorphism exists on the BDNF gene in 30-50% of the human population that results in an amino acid change from valine (val) to methionine (met) at position 66 (val66met) of the precursor peptide proBDNF. The presence of the met allele results in a 25% reduction in activity-dependent secretion of BDNF in the CNS.

The Wellness in Rehabilitation program at the VA Palo Alto Health Care System is a lifestyle medicine intervention for patients following stroke. It is a 12-week program involving weekly meetings that include exercise (particularly aerobic exercise), nutrition, stress management, education, and group support. Participants are encouraged to perform healthy lifestyle behaviors (i.e. exercise) daily at home, and a health coach calls each patient weekly to support the behavior change process.

Participants in the Wellness in Rehabilitation program who elect to participate in the research study will have blood drawn at baseline, week 6, and week 12. Blood draws will be performed in the morning prior to exercise, and week 6 will additionally include a blood draw within 30 minutes of completing a bout of aerobic exercise. Following completion of the study, plasma BDNF levels (measured as nanograms per milliliter) will then be measured at all 4 time points (baseline, week 6 pre-exercise, week 6 post-exercise, and week 12). In addition, BDNF genotype will be measured using the baseline sample. Participants will also complete bike or treadmill exercise testing at baseline and week 12 to determine pre- and post-program cardiovascular fitness levels (measured as VO2 max and estimated metabolic equivalents), and will also complete a 6-minute walk test. They will be asked to record their exercise daily and will additionally complete the Physical Activity Scale for Individuals with Physical Disabilities at baseline and week 12 time points.

Conditions

Stroke

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Post-stroke

Patients will receive a 12-week lifestyle medicine program.

Group Type: EXPERIMENTAL

Wellness in Rehabilitation program

Intervention Type: BEHAVIORAL

The 12-week Wellness in Rehabilitation program includes weekly in-person meetings including aerobic exercise, nutrition/cooking training, stress management techniques, education, and group support. A health coach will facilitate continuation of healthy behaviors at home.

Interventions

Wellness in Rehabilitation program

The 12-week Wellness in Rehabilitation program includes weekly in-person meetings including aerobic exercise, nutrition/cooking training, stress management techniques, education, and group support. A health coach will facilitate continuation of healthy behaviors at home.

Intervention Type: BEHAVIORAL

Other Intervention Names

Lifestyle Medicine program

Eligibility Criteria

Inclusion Criteria

• History of prior stroke (ischemic or hemorrhagic) or transient ischemic attack
• Ability to ambulate at least 10 feet with minimal to moderate assistance
• Ability to travel to intervention site on a weekly basis.

Exclusion Criteria

• Cerebral aneurysm
• Concurrent pregnancy
• Serious terminal illnesses (e.g. end stage renal disease, heart failure (class IV), cirrhosis (class C), metastatic cancer)
• Any injury or illness preventing participation in regular aerobic exercise
• Moderate-severe dementia or cognitive decline

• Minimum Eligible Age: 30 Years
• Maximum Eligible Age: 90 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Stanford University

OTHER

Sponsor Role: collaborator

Spaulding Rehabilitation Hospital

OTHER

Sponsor Role: collaborator

VA Palo Alto Health Care System

FED

Sponsor Role: lead

Responsible Party

Jeffrey Krauss

Staff Physician

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Jeffrey Krauss, MD

Role: PRINCIPAL_INVESTIGATOR

VA Palo Alto Health Care System, Stanford University

Locations

VA Palo Alto Health Care System

Palo Alto, California, United States

Site Status: RECRUITING

Countries

United States

Central Contacts

Jeffrey Krauss, MD

Role: CONTACT

jkrauss@stanford.edu

6504935000 ext. 65525

Windy McNerney, PhD

Role: CONTACT

windymc@stanford.edu

6504935000

Facility Contacts

Jeffrey Krauss, MD

Role: primary

jeffrey.krauss@va.gov

650-493-5000 ext. 65525

Other Identifiers

KRU001

Identifier Type: -

Identifier Source: org_study_id