Studying the effect of Kyphologic and Maria Adelaide Orthoses on the Sagittal Spinal Curves

Studying the effect of Kyphologic and Maria Adelaide Orthoses on the Sagittal Spinal Curves in people with Scheuermann’s Kyphosis: a randomized clinical trial

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20241013063348N1

Enrollment

Registered

2024-12-04

Start date

2024-12-20

Completion date

Unknown

Last updated

2025-07-21

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

Conditions

Scheuermann’s Kyphosis.

Interventions

Intervention 1: Test group: Kyphologic Orthosis? It is a thermoplastic TLSO orthosis that extends anteriorly from the cavity of the Coracoid appendage to the symphysis pubis and posteriorly from the a

Eligibility

Sex/Gender

All

Age

8 Years to 16 Years

Inclusion criteria

Inclusion criteria: The kyphosis angle of the thoracic or thoracolumbar region is more than 45 degrees Risser sign is between zero and two The apex of the arch is at T7 or lower There should be no prohibition to use an orthosis

Exclusion criteria

Exclusion criteria: The kyphosis angle of the thoracic region should be more than 75 degrees In addition to kyphosis, have scoliosis have musculoskeletal, neurological or metabolic diseases at the same time BMI is more than 30 Deformity of the spine is congenital Have a history of spine surgery

Design outcomes

Primary

Measure	Time frame
Cervical Lordosis Angle. Timepoint: Before, one month and six months after the intervention. Method of measurement: EOS radiography device operator software.;Thoracic Kyphosis Angle. Timepoint: Before, one month and six months after the intervention. Method of measurement: EOS radiography device operator software.;Lumbar Lordosis Angle. Timepoint: Before, one month and six months after the intervention. Method of measurement: EOS radiography device operator software.;Sagittal Vertical Axis. Timepoint: Before, one month and six months after the intervention. Method of measurement: EOS radiography device operator software.;Sacral Inclination Angle. Timepoint: Before, one month and six months after the intervention. Method of measurement: EOS radiography device operator software.;Pelvic Tilt Angle. Timepoint: Before, one month and six months after the intervention. Method of measurement: EOS radiography device operator software.	—

Measure

Time frame

Cervical Lordosis Angle. Timepoint: Before, one month and six months after the intervention. Method of measurement: EOS radiography device operator software.;Thoracic Kyphosis Angle. Timepoint: Before, one month and six months after the intervention. Method of measurement: EOS radiography device operator software.;Lumbar Lordosis Angle. Timepoint: Before, one month and six months after the intervention. Method of measurement: EOS radiography device operator software.;Sagittal Vertical Axis. Timepoint: Before, one month and six months after the intervention. Method of measurement: EOS radiography device operator software.;Sacral Inclination Angle. Timepoint: Before, one month and six months after the intervention. Method of measurement: EOS radiography device operator software.;Pelvic Tilt Angle. Timepoint: Before, one month and six months after the intervention. Method of measurement: EOS radiography device operator software.

—

Secondary

Measure	Time frame
Satisfaction score. Timepoint: Six months after the intervention. Method of measurement: Questionnaire survey of orthosis and prosthesis users.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Ebrahim Sadeghi

Esfahan University of Medical Sciences

sadeghi@rehab.mui.ac.ir+98 31 3792 5096

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026