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6 Minute Propulsion Test Sensitivity to Increased Aerobic Capacity

6 Minute Propulsion Test Sensitivity to Increased Aerobic Capacity

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01184729
Enrollment
27
Registered
2010-08-19
Start date
2008-11-30
Completion date
2013-09-30
Last updated
2014-07-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Spinal Cord Injury

Keywords

aerobic capacity

Brief summary

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

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.

Interventions

None listed

Sponsors

University of Miami
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Change in Oxygen uptake during 6 min Push Test From baseline.Visits 1-4Subjects will be prepared by putting a flexible mask over the mouth and nose. Heart rate during testing will be monitored by either three electrodes on the chest or by a monitor strapped around the chest. Heart rate and oxygen consumption during each 6MPT will be measured. Participants will be instructed to propel as far as possible on a 30m loop marked at 3m intervals, with 15m between pylons, and two 180 degree turns. Distance traveled in 6 minutes (m) will be computed by multiplying the number of full laps completed by 15m and adding the distance traveled in the last lap.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026