6 Minute Push & 30 Second Sprint Tests Reliability & Relationship to Fitness, Participation, & Environmental Assessments
NCT ID: NCT01184742
Last Updated: 2014-07-22
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
56 participants
OBSERVATIONAL
2010-03-31
2014-01-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
6 Minute Propulsion Test Sensitivity to Increased Aerobic Capacity
NCT01184729
Wheelchair Mobility Assessment of Individuals With Spinal Cord Injury
NCT01204047
Design and Delivery Preferences for Exercise Intervention in People With Spinal Cord Injury
NCT06578780
Enhancing Indoor, Community, and Advanced Wheelchair Skills in Spinal Cord Injury (SCI)
NCT00434018
Manual Wheelchair Speed, Maneuverability, and Endurance and Community Access
NCT03469414
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
CASE_ONLY
CROSS_SECTIONAL
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* able to self-propel a manual wheelchair
* spinal cord injury between C5 and T5
Exclusion Criteria
* spinal cord injury severity of AIS D
* unstable angina or myocardial infarction within the past month
* resting heart rate \>120
* systolic blood pressure \>180 mm Hg, or diastolic blood pressure \>100 mm HG
18 Years
65 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Paralyzed Veterans of America
OTHER
University of Miami
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Mark S. Nash, Ph.D., FACSM
Professor
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Mark S Nash, PhD
Role: PRINCIPAL_INVESTIGATOR
University of Miami, The Miami Project to Cure Paralysis
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
The Miami Project to Cure Paralysis
Miami, Florida, United States
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
TMP-MN-001
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.