6 Minute Propulsion Test Sensitivity to Increased Aerobic Capacity

NCT ID: NCT01184729

Last Updated: 2014-07-22

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

27 participants

Study Classification

OBSERVATIONAL

Study Start Date

2008-11-30

Study Completion Date

2013-09-30

Brief Summary

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The goals of this project are to 1)determine the responsiveness of the 6 Minute Push Test (6MPT) and 2) explore the relationship between 6MPT distance and measures of handicap, wheelchair satisfaction, depression, and self-reported avoidance of environmental features.

Detailed Description

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The 6 minute walk test is a widely used assessment of aerobic capacity, function, and functional change in the ambulatory population. A similar clinical and research outcome instrument that is responsive to changes in aerobic capacity and function are lacking for persons with spinal cord injury (SCI). A 6 minute push test, adapted from the 6 minute walk test may fill the void. The primary aim of this project is to assess if distance traveled in 6 minutes of wheelchair propulsion changes after an increase in aerobic capacity. We hypothesize that participants will push farther in 6 minutes after their aerobic capacity increases. The secondary aim is to explore the correlation between 6MPT distance and handicap, depression, wheelchair satisfaction, and self-reported avoidance of environmental features. We hypothesize increasing 6MPTdistance will be correlated with decreasing depression, decreasing handicap, decreasing self-reported avoidance of environmental features, and increasing wheelchair satisfaction. This is a low risk, high benefit study.

Conditions

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Spinal Cord Injury

Study Design

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Observational Model Type

CASE_ONLY

Study Time Perspective

PROSPECTIVE

Study Groups

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Spinal Cord Injury

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

* T1 or lower injury
* at least 1 year post-injury
* able to self-propel a manual wheelchair
* enrolled in TMP-MN-006

Exclusion Criteria

* Not enrolled in the IRB approval parent study, "Exercise Treatment of Obesity-Related Secondary Conditions in Adults with Paraplegia", TMP-MN-006
* Unstable angina or myocardial infarction within the past month
* Resting heart rate \>120
* Systolic blood pressure \> 180 mm Hg
* Diastolic blood pressure \> 100 mm Hg
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University of Miami

OTHER

Sponsor Role lead

Responsible Party

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Mark S. Nash, Ph.D., FACSM

Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Mark S Nash, PhD

Role: PRINCIPAL_INVESTIGATOR

University of Miami, The Miami Project to Cure Paralysis

Locations

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The Miami Project to Cure Paralysis

Miami, Florida, United States

Site Status

Countries

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United States

Other Identifiers

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TMP MN 002

Identifier Type: -

Identifier Source: org_study_id

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