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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06027580
Other study ID # PRO00048530
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date February 21, 2024
Est. completion date December 31, 2025

Study information

Verified date March 2024
Source Medical College of Wisconsin
Contact Stacy Stibb, DO
Phone 414-266-2745
Email sstibb@mcw.edu
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of this study is to determine the impact of the SPIO® Core-MAX® Expedition orthosis on an infant's head, trunk and upper limb function.


Description:

This study will observe the difference in outcomes between two courses of standard clinical care: therapy or therapy with the SPIO® Core-MAX® Expedition orthosis. Families will self-select that standard care option that works best for their family, and outcomes will be observed at baseline, 3 months and 6 months.


Recruitment information / eligibility

Status Recruiting
Enrollment 30
Est. completion date December 31, 2025
Est. primary completion date June 30, 2025
Accepts healthy volunteers No
Gender All
Age group 6 Months to 18 Months
Eligibility Inclusion Criteria: - Study subjects aged 6 months to 18 months age corrected with abnormal muscle tone - No previous use of SPIO® or similar Lycra/compression garments - Assessed by provider as likely to benefit from use of compression garment Exclusion Criteria: - Non-English speaking - Inability for family to bring study subject to assessments - Orthosis or casting that contraindicate SPIO® Core-MAX® during the study period - Botulinum toxin injections within 3 months, or during study participation - Having prior orthopedic or neurosurgery surgeries within one year

Study Design


Related Conditions & MeSH terms


Intervention

Device:
SPIO® Core-MAX® Expedition thoracolumbosacral orthosis
SPIO® Core-MAX® Expedition thoracolumbosacral orthosis use 2 hours per day for 6 months

Locations

Country Name City State
United States Medical College of Wisconsin/Children's Wisconsin Milwaukee Wisconsin

Sponsors (2)

Lead Sponsor Collaborator
Medical College of Wisconsin SPIO

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in head and trunk position from centerline at baseline, 3-months and 6-months. Degree change in head and trunk position from centerline as assessed by motion capture. Through study completion, an average of 2 years
Primary Change from baseline to 3-months and 6-months on the Pediatric Quality of Life Inventory Infant Scale. The Pediatric Quality of Life Inventory Infant Scales (PedQL-I) is used to assess parent-reported health-related quality of life for children with ages 1-12 months or 12-24 months. It has the same five components, including physical functioning (6 items), physical symptoms (10 items), emotional functions (12 items), social functioning (4 items), and cognitive functioning (4 items) with scale from 0 to 4.
0 if it is never a problem
if it is almost never a problem
if it is sometimes a problem
if it is often a problem
if it is almost always a problem
Through study completion, an average of 2 years
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