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

NCT05251740 · ClinicalTrials.gov registry record · NA

Impact of a Standing Program in a Child With Spina Bifida: A Case Report

A NA study, sponsored by University of St. Augustine for Health Sciences.

Completed
Registry status
NA
Development phase
1
Enrollment target

NCT05251740: Completed NA study, sponsored by University of St. Augustine for Health Sciences.

NCT05251740 is a NA study that has completed, run by University of St. Augustine for Health Sciences. The registered enrollment target is 1 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (100% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT05251740, a NA study, has completed, sponsored by University of St. Augustine for Health Sciences.

COMPLETED
Registry status
NA
Development phase
1 participants
Enrollment target

Study Summary

The purpose of this case study is to investigate a child with MMC who has significant knee and hip flexion contractures to answer the following research questions: 1) Is a home standing program effective in reducing hip and knee flexion contractures in a child with MMC? 2) Does a home standing program result in a change in the quality of functional movement? A Physical therapist, PT, will administer the Peds NRS and goniometric measurements prior to the start of the study and at the end of the study. The PT will also provide the parent instruction on the standing home program with weekly check-ins to ensure the parent and child are able to follow the home program. The home standing program will last 8 weeks. The parent will keep a written log of stander use. The Peds NRS scores and goniometric measurements will be compared pre and post intervention. The expected outcome is that the Peds NRS scores and hip and knee extension range of motion measurements will improve.

Primary Outcome

A universal goniometer will be used to measure the child's hip and knee joint passive ranges of motion (PROM).

Interventions

  • DEVICE Altimate Medical EasyStand Bantam

Trial Details

FieldValue
Enrollment Target 1 participants
Start Date 2021-05-06
Est. Completion 2021-07-08
Phase NA

What the finished NCT05251740 record still lists

NCT05251740 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 1 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (100% lower).

The record links to 0 conditions, and to 1 intervention - of which Altimate Medical EasyStand Bantam is the first listed.

NCT05251740 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT05251740 about?

NCT05251740 is a clinical study titled "Impact of a Standing Program in a Child With Spina Bifida: A Case Report". The purpose of this case study is to investigate a child with MMC who has significant knee and hip flexion contractures to answer the following research questions: 1) Is a home standing program effective in reducing hip and knee flexion contractures in a child with MMC? 2) Does a home standing progr...

What is the current status of trial NCT05251740?

This trial is currently completed. It is a NA study. The enrollment target is 1 participants. The study started on 2021-05-06. Estimated completion is 2021-07-08.

What interventions are being tested in trial NCT05251740?

The interventions under investigation include: Altimate Medical EasyStand Bantam (DEVICE).

Who is sponsoring clinical trial NCT05251740?

This trial is sponsored by University of St. Augustine for Health Sciences, which has 6 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT05251740's enrollment target sits among peer trials

1 2001st of 2000 the lowest 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 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 NCT05251740, the US trial registry maintained by the National Library of Medicine. NCT05251740 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.