Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT00270855 · ClinicalTrials.gov registry record · NA

Exercise to Reduce Obesity in Spinal Cord Injury

A NA study, sponsored by VA Office of Research and Development.

Completed
Registry status
NA
Development phase
29
Enrollment target

NCT00270855: Completed NA study, sponsored by VA Office of Research and Development.

NCT00270855 is a NA study that has completed, run by VA Office of Research and Development. The registered enrollment target is 29 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist → Add completion date to calendar (.ics) →

The verdict

NCT00270855, a NA study, has completed, sponsored by VA Office of Research and Development.

COMPLETED
Registry status
NA
Development phase
29 participants
Enrollment target

Study Summary

The purpose of this proposal was to evaluate and compare the health benefits of using upper extremity exercise versus functional electrical stimulation for lower extremity exercise. It was our hypothesis that both Functional Electrical Stimulation Leg Cycle Ergometry (FES LCE) exercise and voluntary Arm Crank Ergometry (ACE) upper extremity exercise would increase whole body energy expenditure, thereby increasing muscle mass, insulin sensitivity, glucose effectiveness and improving lipid profiles in adults with paraplegia.

Primary Outcome

Change in % Body Fat after 16 week intervention. Change score was calculated as final value (i.e., post intervention variable) minus baseline value.

Interventions

  • PROCEDURE Arm Crank Ergometry
  • PROCEDURE FES Cycle Ergometer

Trial Details

FieldValue
Enrollment Target 29 participants
Start Date 2008-05
Est. Completion 2011-12
Phase NA
VA Office of Research and Development

1,668 total trials

What the finished NCT00270855 record still lists

NCT00270855 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 29 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower).

The record links to 0 conditions, and to 2 interventions - of which Arm Crank Ergometry is the first listed.

NCT00270855 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00270855 about?

NCT00270855 is a clinical study titled "Exercise to Reduce Obesity in Spinal Cord Injury". The purpose of this proposal was to evaluate and compare the health benefits of using upper extremity exercise versus functional electrical stimulation for lower extremity exercise. It was our hypothesis that both Functional Electrical Stimulation Leg Cycle Ergometry (FES LCE) exercise and voluntary...

What is the current status of trial NCT00270855?

This trial is currently completed. It is a NA study. The enrollment target is 29 participants. The study started on 2008-05. Estimated completion is 2011-12.

What interventions are being tested in trial NCT00270855?

The interventions under investigation include: Arm Crank Ergometry (PROCEDURE), FES Cycle Ergometer (PROCEDURE).

Who is sponsoring clinical trial NCT00270855?

This trial is sponsored by VA Office of Research and Development, which has 1,668 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00270855's enrollment target sits among peer trials

29 1702nd of 2000 higher than 297 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT02429557 · 29 participants · Phase 1

    Hemodynamic Mechanisms of Abdominal Compression in the Treatment of Orthostatic Hypotension in Autonomic Failure

  • NCT02568878 · 29 participants · Phase 3

    Creatine for Depressed Male and Female Methamphetamine Users

  • NCT03014401 · 29 participants · NA

    The Effect of Adipose-Derived Stem Cells for Knee Osteoarthritis

  • NCT03128996 · 29 participants · Phase 1

    Reduced Intensity Conditioning and Familial HLA-Mismatched BMT for Non-Malignant Disorders

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT00270855, the US trial registry maintained by the National Library of Medicine. NCT00270855 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.