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

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05251740
Enrollment
1
Registered
2022-02-23
Start date
2021-05-06
Completion date
2021-07-08
Last updated
2022-02-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Spina Bifida With Hydrocephalus

Brief 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.

Interventions

The child will stand in the device for 60 min per day, 5 days per week for 2 months.

Sponsors

University of St. Augustine for Health Sciences
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

Single participant case study

Eligibility

Sex/Gender
FEMALE
Age
9 Years to 9 Years
Healthy volunteers
Yes

Inclusion criteria

* diagnosis of Spina Bifida * be able to stand with an assistive device

Exclusion criteria

* a diagnosis unrelated to Spina Bifida that limits standing * medical restrictions that contraindicate standing

Design outcomes

Primary

MeasureTime frameDescription
Goniometric measurementsAt 0 weeksA universal goniometer will be used to measure the child's hip and knee joint passive ranges of motion (PROM).
Pediatric Neuromuscular Recovery Scale (Peds NRS)At 0 weeksThe Pediatric Neuromuscular Recovery Scale (Peds NRS) assesses the quality of functional movement in children with MMC ages 1-12years. The Peds NRS examines the quality of sitting, upper extremity function, standing, and walking.The examiner administers the Peds NRS using a height-adjustable bench, mat table, fine motor manipulatives, and a ball. The examiner scores each of the 13 items on the Peds NRS on a 12-point scale, with one point allocated to each of the 12 phases of the item. The examiner scores the highest phase achieved by the child. A summary score is obtained using the sum of the items.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026