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Constructive Variations of Classic Orthopedic Braces for Spinal Deformity During Growth

Constructive Variations of Classic Orthopedic Braces for Spinal Deformity During Growth: Efficacy Analysis of a Retrospective Cohort

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04904627
Enrollment
470
Registered
2021-05-27
Start date
2021-07-01
Completion date
2024-12-31
Last updated
2024-05-08

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

Conditions

Scoliosis

Brief summary

The construction methods of the same brace vary on an experiential basis according to who builds them, the prescriber, the characteristics of the patients and also the innovations introduced to ensure greater comfort for the patient. The closure of the brace or the way in which the two shells are fixed varies at the discretion of the orthopedic technician. Plastic materials have also changed. In addition, the use of the classic cast for the production of the negative model was gradually replaced by cad-cam technology. In some cases, modular constructions were introduced with respect to the customized one. All this has changed the classic corsets over time, even without changing their name / type, and according to the hypothesis that their effectiveness remained at least the same, if not even improved. There are no publications that have shown variations in efficacy that can be correlated with some of these stylistic variations. The purpose of this study is to retrospectively investigate whether the various innovations and stylistic variations over time have had an effect on the clinical, functional and radiographic outcomes in growing subjects suffering from spinal deformity treated with corsets at a specialized center.

Interventions

None listed

Sponsors

Istituto Scientifico Italiano Colonna Vertebrale
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
No minimum to 16 Years
Healthy volunteers
No

Inclusion criteria

* Idiopathic adolescent scoliosis and/or dorsal hyperkyphosis, * age under 16 years at the start of observation, * brace prescription for more than 18 hours/day, * availability of radiographs of the entire spine while standing and in brace radiographs at 1 month or out of brace at 5 ± 2 months at the end growth after 48 hours without brace and at 1 year. * availability of compliance data * Risser between 0 and 4 at first assessment

Exclusion criteria

* All secondary causes of scoliosis * history of spinal fusion surgery * lack of one of the radiographic examinations required by the protocol

Design outcomes

Primary

MeasureTime frameDescription
Changes in radiographic measurementspre-treatment, in brace after a month from the start of wearing and without brace after 5 ± 2 months, after an average period of 4 years +/-2 , after 48 hours without brace and 1 year later.variation of Cobb degrees of the main curve in the frontal plane over time

Secondary

MeasureTime frameDescription
HRQOLpre-treatment, after a month from the start of brace wearing, after 5 ± 2 months, after an average period of 4 years +/-2 , and 1 year latermeasures of quality of life. The Italian Spine Youth Quality of Life questionnaire (ISYQOL) measures the health-related quality of life of adolescents with spinal deformities. ISYQOL consists of 20 items, each scored 0, 1 or 2. In accordance with the Rasch analysis technique, used to develop the questionnaire, the ordinal ISYQOL total score is converted to an interval measure (i.e., ISYQOL measure), which is expressed on a 0%-100% scale (with 100% indicating high quality of life).
Treatment outcomeafter an average period of 4 years +/-2variation of the main curve of at least 5 Cobb degrees, end treatment results: main curve \</=30 Cobb degrees, main curve \</=45 Cobb degrees, and main curve \>50 Cobb degrees
Treatment complianceafter a month from the start of brace wearing, after 5 ± 2 months, and after an average period of 4 years +/-2Treatment compliance measures: percentage of brace wearing declared and measured by heat sensors
Deformity clinical measurespre-treatment, after a month from the start of brace wearing, after 5 ± 2 months,after an average period of 4 years +/-2 , and 1 year laterscore on the evaluation of the aesthetic profile of the trunk (TRACE)

Countries

Italy

Outcome results

None listed

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