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

NCT03495752 · ClinicalTrials.gov registry record · NA

The Effect of Fatigue on the Forward-Step-Down Test

A NA study, sponsored by Louisiana State University Health Sciences Center Shreveport.

Completed
Registry status
NA
Development phase
18
Enrollment target

NCT03495752: Completed NA study, sponsored by Louisiana State University Health Sciences Center Shreveport.

NCT03495752 is a NA study that has completed, run by Louisiana State University Health Sciences Center Shreveport. The registered enrollment target is 18 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT03495752, a NA study, has completed, sponsored by Louisiana State University Health Sciences Center Shreveport.

COMPLETED
Registry status
NA
Development phase
18 participants
Enrollment target

Study Summary

This study investigates the effect that performing a cardiovascular maximum effort test (the Bruce treadmill protocol) has on performance of the Forward-Step-Down Test (FSDT). The FSDT is performed prior to the fatigue protocol as a baseline measurement, then at 1, 5, and 10 minutes after the fatigue protocol. Participants much reach a certain heart rate (within 10 bpm) of their age predicted maximum heart rate to ensure that the fatigue protocol reaches a maximum fatiguing effort.

Primary Outcome

The participants' scores on the pre-test FSDT will be compared to their scores post-test measured at 1, 5, and 10 minutes after the fatigue stimulus

Interventions

  • OTHER Bruce Fatigue Protocol

Trial Details

FieldValue
Enrollment Target 18 participants
Start Date 2018-06-21
Est. Completion 2019-06-29
Phase NA

What the finished NCT03495752 record still lists

NCT03495752 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 18 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower).

The record links to 0 conditions, and to 1 intervention - of which Bruce Fatigue Protocol is the first listed.

NCT03495752 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03495752 about?

NCT03495752 is a clinical study titled "The Effect of Fatigue on the Forward-Step-Down Test". This study investigates the effect that performing a cardiovascular maximum effort test (the Bruce treadmill protocol) has on performance of the Forward-Step-Down Test (FSDT). The FSDT is performed prior to the fatigue protocol as a baseline measurement, then at 1, 5, and 10 minutes after the fatigu...

What is the current status of trial NCT03495752?

This trial is currently completed. It is a NA study. The enrollment target is 18 participants. The study started on 2018-06-21. Estimated completion is 2019-06-29.

What interventions are being tested in trial NCT03495752?

The interventions under investigation include: Bruce Fatigue Protocol (OTHER).

Who is sponsoring clinical trial NCT03495752?

This trial is sponsored by Louisiana State University Health Sciences Center Shreveport, which has 40 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03495752's enrollment target sits among peer trials

18 1863rd of 2000 higher than 130 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

  • NCT01245179 · 18 participants · Phase 1

    Study of Panobinostat (LBH589) in Patients With Sickle Cell Disease

  • NCT01999361 · 18 participants · NA

    Prevention of de Novo Allosensitization in Islet Transplant Recipients Following Complete Graft Loss

  • NCT02359825 · 18 participants · Phase 1

    Nerve Repair Using Hydrophilic Polymers to Promote Immediate Fusion of Severed Axons and Swift Return of Function

  • NCT02870244 · 18 participants · Phase 1

    Adoptive T Cell Immunotherapy for Advanced Melanoma Using Engineered Lymphocytes

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT03495752, the US trial registry maintained by the National Library of Medicine. NCT03495752 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.