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

NCT04855032 · ClinicalTrials.gov registry record · NA

Post-stroke Perturbation Training

A NA study of Stroke, sponsored by Medical University of South Carolina.

Completed
Registry status
NA
Development phase
86
Enrollment target
1
Study location

NCT04855032: Completed NA study of Stroke, sponsored by Medical University of South Carolina.

NCT04855032 is a NA study of Stroke that has completed, run by Medical University of South Carolina. The registered enrollment target is 86 participants, below the 12,016-participant average among 454 other Stroke trials with a reported enrollment target (99% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT04855032, a NA study of Stroke, has completed, sponsored by Medical University of South Carolina.

COMPLETED
Registry status
NA
Development phase
86 participants
Enrollment target
1
Study location

Study Summary

Following a stroke, many individuals have a high risk of falls, which can negatively influence quality of life. Unfortunately, current treatments have not effectively addressed this problem. This study investigates whether two methods of delivering mechanical perturbations during walking have the potential to improve post-stroke walking balance and reduce real-world fall incidence.

Primary Outcome

A fall will be defined as an event in which a participant loses their balance and comes to rest on the ground, floor, or lower level. Falls will be measured during the 12-week periods preceding and following the intervention, using 2-week calendars on postcards to be sent to the investigators.

Conditions Studied

Interventions

  • BEHAVIORAL Reactive Perturbations
  • BEHAVIORAL Proactive Perturbations

Study Locations (1)

South Carolina

  • Medical University of South Carolina - Charleston

Trial Details

FieldValue
Enrollment Target 86 participants
Start Date 2021-10-06
Est. Completion 2025-12-05
Phase NA

What the finished NCT04855032 record still lists

NCT04855032 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 86 participants, a relatively small participant target, below the 12,016-participant average among 454 other Stroke trials with a reported enrollment target (99% lower).

The record links to 1 condition, with Stroke appearing as the primary indexed condition, and to 2 interventions - of which Reactive Perturbations is the first listed.

NCT04855032 reports a single indexed study location in South Carolina.

Frequently Asked Questions

What is clinical trial NCT04855032 about?

NCT04855032 is a clinical study titled "Post-stroke Perturbation Training". Following a stroke, many individuals have a high risk of falls, which can negatively influence quality of life. Unfortunately, current treatments have not effectively addressed this problem. This study investigates whether two methods of delivering mechanical perturbations during walking have the po...

What is the current status of trial NCT04855032?

This trial is currently completed. It is a NA study. The enrollment target is 86 participants. The study started on 2021-10-06. Estimated completion is 2025-12-05.

What conditions does trial NCT04855032 study?

This clinical trial studies the following conditions: Stroke.

What interventions are being tested in trial NCT04855032?

The interventions under investigation include: Reactive Perturbations (BEHAVIORAL), Proactive Perturbations (BEHAVIORAL).

Who is sponsoring clinical trial NCT04855032?

This trial is sponsored by Medical University of South Carolina, which has 755 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT04855032 being conducted?

This trial has 1 study location across South Carolina. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Stroke

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT04855032's enrollment target sits among peer trials

86 161st of 454 higher than 294 of 454 other Stroke trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Stroke 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

  • NCT01639508 · 86 participants · Phase 2

    Cabozantinib in Patients With RET Fusion-Positive Advanced Non-Small Cell Lung Cancer and Those With Other Genotypes: ROS1 or NTRK Fusions or Increased MET or AXL Activity

  • NCT03519269 · 86 participants · NA

    Navio Robotic Versus Conventional Total Knee Arthroplasty

  • NCT04132999 · 86 participants · NA

    PAP for Children With DS and OSAS

  • NCT04545957 · 86 participants · NA

    Jump: MR Simulation For Radiation Therapy Master Protocol

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 NCT04855032, the US trial registry maintained by the National Library of Medicine. NCT04855032 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.