Clinical Trials Directory

Trials / Completed

CompletedNCT05251740

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

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
1 (actual)
Sponsor
University of St. Augustine for Health Sciences · Academic / Other
Sex
Female
Age
9 Years – 9 Years
Healthy volunteers
Accepted

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.

Conditions

Interventions

TypeNameDescription
DEVICEAltimate Medical EasyStand BantamThe child will stand in the device for 60 min per day, 5 days per week for 2 months.

Timeline

Start date
2021-05-06
Primary completion
2021-07-08
Completion
2021-07-08
First posted
2022-02-23
Last updated
2022-02-23

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT05251740. Inclusion in this directory is not an endorsement.