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Remote Limb Ischemic Conditioning to Enhance Learning and Muscle Strength in Healthy Young Adults

Primary Purpose

Healthy, Young Adults

Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
RLIC
Sham conditioning
Muscle strength training
Driving training
Balance training
Sponsored by
Washington University School of Medicine
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Healthy, Young Adults focused on measuring ischemic conditioning, motor learning, strength, cognition

Eligibility Criteria

18 Years - 40 Years (Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  1. Healthy adults between the age of 18 and 40 years
  2. Visual acuity of 20/20 with corrected vision

Exclusion Criteria:

  1. History of neurological condition (i.e. stroke, Alzheimer's disease, Parkinson's disease), Attention Deficit Hyperactivity Disorder (ADHD), depression, bipolar disorder, balance impairment, or vestibular disorder
  2. History of severe motion sickness, moderate to severe motion sickness or nausea on oculo-motor components of Simulator sickness questionnaire, inability to ride a car, boat, train or airplane due to motion sickness
  3. Recent wrist, hand or forearm injury that would currently prevent ability to lift weights
  4. History of lower extremity condition, injury, or surgery that would currently impair ability to stand or balance
  5. Any extremity soft tissue, orthopedic, or vascular injury (i.e. peripheral vascular disease) which may contraindicate RLIC
  6. Any cognitive, sensory, or communication problem that would prevent completion of the study
  7. History of or current sleep apnea
  8. Current intensive weight lifting or interval training exercise
  9. Current substance abuse or dependence
  10. Unwillingness to travel for all study visits

Sites / Locations

  • Washington University School of Medicine

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Sham Comparator

Arm Label

Remote Limb Ischemic Conditioning (RLIC)

Sham Conditioning

Arm Description

RLIC is achieved via blood pressure cuff inflation to 20 mmHg above systolic blood pressure on the dominant arm. RLIC requires 45 minutes and involves 5 cycles of 5 minutes blood pressure cuff inflation followed by alternating 5 minutes of cuff deflation. RLIC is performed on visits 1-8.

Sham conditioning is achieved via blood pressure cuff inflation to 10 mmHg under diastolic blood pressure on the dominant arm. Sham conditioning requires 45 minutes and involves 5 cycles of 5 minutes blood pressure cuff inflation followed by alternating 5 minutes of cuff deflation. Sham conditioning is performed on visits 1-8.

Outcomes

Primary Outcome Measures

One-repetition Maximum of Wrist Extensors
The maximum amount of force (lbs) that a participant can generate while performing one wrist extension movement.

Secondary Outcome Measures

Full Information

First Posted
April 16, 2018
Last Updated
January 22, 2020
Sponsor
Washington University School of Medicine
Collaborators
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
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1. Study Identification

Unique Protocol Identification Number
NCT03512028
Brief Title
Remote Limb Ischemic Conditioning to Enhance Learning and Muscle Strength in Healthy Young Adults
Official Title
Effects of Remote Limb Ischemic Conditioning to Enhance Performance, Cognitive-motor Learning and Muscle Strength in Healthy Young Adults
Study Type
Interventional

2. Study Status

Record Verification Date
January 2020
Overall Recruitment Status
Completed
Study Start Date
November 8, 2017 (Actual)
Primary Completion Date
December 31, 2018 (Actual)
Study Completion Date
January 31, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Washington University School of Medicine
Collaborators
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this research study is to determine if remote limb ischemic conditioning (RLIC) can enhance learning of a motor (balance) and an ecologically valid, complex cognitive-motor (driving) task, and increase skeletal muscle strength in neurologically-intact young adults.
Detailed Description
Ischemic conditioning is an endogenous phenomenon in which exposing a target organ or tissue to one or more brief episodes of ischemia results in protection of that organ against subsequent ischemia. The effects of ischemic conditioning are not confined within an organ but can be can be transferred from one organ to another, a technique called remote ischemic conditioning. A clinically feasible method for this is remote limb ischemic conditioning (RLIC), where episodes of ischemia and perfusion are induced with a blood pressure cuff placed on the arm. The overall goal of this line of work is to use ischemic conditioning to enhance learning and outcomes in persons with neurologic injuries. Two previous studies have shown that remote limb ischemic conditioning (RLIC) can enhance learning a motor task in healthy young adults. The current study extends that work to determine if RLIC enhances muscle strength training and a complex cognitive-motor task (simulated driving). This Phase I study will yield the necessary information to design and execute subsequent trials in neurologic patient populations.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Healthy, Young Adults
Keywords
ischemic conditioning, motor learning, strength, cognition

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Parallel Assignment
Model Description
Single blinded, randomized controlled trial
Masking
Participant
Masking Description
Participants are masked to group assignment (RLIC vs. Sham conditioning).
Allocation
Randomized
Enrollment
34 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Remote Limb Ischemic Conditioning (RLIC)
Arm Type
Experimental
Arm Description
RLIC is achieved via blood pressure cuff inflation to 20 mmHg above systolic blood pressure on the dominant arm. RLIC requires 45 minutes and involves 5 cycles of 5 minutes blood pressure cuff inflation followed by alternating 5 minutes of cuff deflation. RLIC is performed on visits 1-8.
Arm Title
Sham Conditioning
Arm Type
Sham Comparator
Arm Description
Sham conditioning is achieved via blood pressure cuff inflation to 10 mmHg under diastolic blood pressure on the dominant arm. Sham conditioning requires 45 minutes and involves 5 cycles of 5 minutes blood pressure cuff inflation followed by alternating 5 minutes of cuff deflation. Sham conditioning is performed on visits 1-8.
Intervention Type
Behavioral
Intervention Name(s)
RLIC
Other Intervention Name(s)
remote limb ischemic conditioning
Intervention Description
See descriptions under arm/group descriptions. RLIC is delivered for 8 visits. Visits 1-3 occur on consecutive work days and visits 4-8 occur on alternating week days.
Intervention Type
Behavioral
Intervention Name(s)
Sham conditioning
Intervention Description
See descriptions under arm/group descriptions. Sham conditioning is delivered for 8 visits. Visits 1-3 occur on consecutive work days and visits 4-8 occur on alternating week days.
Intervention Type
Behavioral
Intervention Name(s)
Muscle strength training
Intervention Description
All participants undergo muscle strength training of the wrist extensor muscles on one side. Strength training follows standard American College of Sports Medicine guidelines for frequency, intensity, progression etc. Strength training is provided at visits 3-8
Intervention Type
Behavioral
Intervention Name(s)
Driving training
Intervention Description
All participants undergo training of a complex cognitive-motor task using a driving simulator. Participants learn to 'drive' on a virtual course, maximizing speed and minimizing errors. Participants perform the driving task once each day for visits 3-8.
Intervention Type
Behavioral
Intervention Name(s)
Balance training
Intervention Description
All participants undergo training on a balance board, learning to hold the board level with equal weight on each leg. Participants perform the balance task for 15, 30-second trials per day at visits 3-8.
Primary Outcome Measure Information:
Title
One-repetition Maximum of Wrist Extensors
Description
The maximum amount of force (lbs) that a participant can generate while performing one wrist extension movement.
Time Frame
Pre-intervention, post-intervention (2 weeks later), and 1 month post-intervention follow-up

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Healthy adults between the age of 18 and 40 years Visual acuity of 20/20 with corrected vision Exclusion Criteria: History of neurological condition (i.e. stroke, Alzheimer's disease, Parkinson's disease), Attention Deficit Hyperactivity Disorder (ADHD), depression, bipolar disorder, balance impairment, or vestibular disorder History of severe motion sickness, moderate to severe motion sickness or nausea on oculo-motor components of Simulator sickness questionnaire, inability to ride a car, boat, train or airplane due to motion sickness Recent wrist, hand or forearm injury that would currently prevent ability to lift weights History of lower extremity condition, injury, or surgery that would currently impair ability to stand or balance Any extremity soft tissue, orthopedic, or vascular injury (i.e. peripheral vascular disease) which may contraindicate RLIC Any cognitive, sensory, or communication problem that would prevent completion of the study History of or current sleep apnea Current intensive weight lifting or interval training exercise Current substance abuse or dependence Unwillingness to travel for all study visits
Facility Information:
Facility Name
Washington University School of Medicine
City
Saint Louis
State/Province
Missouri
ZIP/Postal Code
63108
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
After completion of the study, all of the individual participant data after deidentification will be submitted to Washington University data repository.
IPD Sharing Time Frame
Following publication of results. No ending date
IPD Sharing Access Criteria
Data will be available to anyone who wishes to access it through Washington University data repository.
IPD Sharing URL
https://openscholarship.wustl.edu

Learn more about this trial

Remote Limb Ischemic Conditioning to Enhance Learning and Muscle Strength in Healthy Young Adults

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