ClinicalTrials.Veeva

Menu

6 Minute Propulsion Test Sensitivity to Increased Aerobic Capacity

University of Miami logo

University of Miami

Status

Completed

Conditions

Spinal Cord Injury

Study type

Observational

Funder types

Other

Identifiers

NCT01184729
TMP MN 002

Details and patient eligibility

About

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.

Full 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.

Enrollment

27 patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

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

Trial design

27 participants in 1 patient group

Spinal Cord Injury

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems