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Scoliosis; Adolescence clinical trials

View clinical trials related to Scoliosis; Adolescence.

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NCT ID: NCT05762354 Completed - Clinical trials for Scoliosis Idiopathic

Investigation of the Relationship Between Body Image Perception, Proprioception, Cobb Angle and Posture in Individuals With Adolescent Idiopathic Scoliosis

Start date: August 26, 2022
Phase:
Study type: Observational

Scoliosis is a three-dimensional torsional deformation of the spine and trunk. Chest deformity and pelvic asymmetry are often seen together with spinal deformity. Adolescent idiopathic scoliosis occurs from the onset of puberty until growth plate closure and is the most common of all scoliosis. One of the most common deformities among posture disorders is known as scoliosis. The change in load distribution resulting from this three-dimensional deformation causes postural changes in patients with idiopathic scoliosis. According to a study, it is thought that postural control and central information processing efficiency may decrease as the Cobb angle increases in people with scoliosis.

NCT ID: NCT05479695 Completed - Scoliosis Clinical Trials

The Effect Insoles on Functional Capacity With Adolescent Idiopathic Scoliosis Using Spinal Orthosis

Start date: May 22, 2021
Phase: N/A
Study type: Interventional

Adolescent Idiopathic Scoliosis; by problem of stabilty causes postural changes, because of this reason patient with scoliosis needs to assesment by risk of balance. Postural adjustments are required, both in a static stance and during walking. Insoles from foot orthoses support better postural balance and control. It has been reported that approximately 87% of scoliosis patients have pelvic asymmetry, and patients with scoliosis with a Cobb angle of 15⁰ or more have balance problems in their feet. Foot orthoses (FO) correct pelvic asymmetry and reduce lower extremity joint angles during walking. In the literature, although there are studies such as balance assessment and plantar pressure analysis in Adolescent Idiopathic Scoliosis (AIS) patients, there are not enough studies on the effect of insoles used in scoliosis patients, and it has been observed that there is no study on the effect of insoles on treatment in patients using spinal orthosis. The aim of this study is to investigate the effect of insoles on the treatment of scoliosis patients using Chêneau type spinal orthosis. In the study; The effect of insoles on patients with 20-45⁰ curvature, adolescent idiopathic scoliosis and using Chêneau type spinal orthosis; It was planned to investigate the groups using and not using insoles at the beginning of the treatment and after 3 months of follow-up by comparing the results of Cobb angle measurement, functional capacity assessment test, quality of life assessment test, balance test and plantar pressure analysis.

NCT ID: NCT05326256 Completed - Clinical trials for Scoliosis Idiopathic

Trunk Proprioception in Adolescent Idiopathic Scoliosis

Start date: February 2, 2022
Phase: N/A
Study type: Interventional

Aims of this clinical research: - To investigate trunk proprioception in all three planes in individuals with adolescent idiopathic scoliosis (AIS), - To investigate the pelvis orientation sense in all three planes in individuals with adolescent idiopathic scoliosis, - To investigate whether trunk proprioception and pelvis orientation sense are improved with Physiotherapy Scoliosis Specific Exercises (PSSE) in AIS, - To investigate whether trunk proprioception and pelvis orientation sense are improved with vestibular exercise training to be added to PSSE exercises in AIS, - Comparison of the effects of different exercise training on trunk proprioception and pelvis orientation sense in AIS - To examine the parameters that may be associated with the improvement of trunk proprioception of different exercise training (health-related quality of life, perception of cosmetic deformity, scoliosis-related clinical features such as Cobb angle, axial trunk rotation, curve type, etc.).

NCT ID: NCT05325463 Completed - Clinical trials for Scoliosis; Adolescence

Lung Recruitment Maneuvers for Postoperative Atelectasis Prevention After Idiopathic Adolescents' Scoliosis Correction

Start date: April 10, 2022
Phase: N/A
Study type: Interventional

The investigators hypothesized that an ultrasound-guided lung recruitment maneuvers would be more effective in preventing postoperative atelectasis than conventional alveolar recruitment after surgical correction of idiopathic adolescent scoliosis.

NCT ID: NCT05259956 Completed - Clinical trials for Scoliosis; Adolescence

Trial on Two Treatments for Adolescent Idiopathic Scoliosis

Start date: February 18, 2022
Phase: N/A
Study type: Interventional

Adolescent Idiopathic scoliosis is a three-dimensional structural deformity of the spine and pelvic that occurs in children. More evidence has arisen to emphasize the important role played by pelvic asymmetry during the progression of scoliosis. The purpose of this study is to compare the effectiveness of pelvic adjustments accompanied with Schroth-based exercises, with the latter alone in adolescent idiopathic scoliosis, to assess the impact of pelvic asymmetry on the spinal three-dimensional parametric features in scoliosis.

NCT ID: NCT05227638 Completed - Clinical trials for Scoliosis; Adolescence

Investigation of the Efficacy of PNF and Schroth Treatment

Start date: November 10, 2021
Phase: N/A
Study type: Interventional

our study was to compare the advantages of Schroth and PNF methods used in AIS treatment

NCT ID: NCT05185050 Completed - Clinical trials for Myofascial Pain Syndrome

Prevalence of Myofascial Pain Syndrome in Adolescent Idiopathic Scoliosis

Start date: October 10, 2021
Phase:
Study type: Observational [Patient Registry]

this is an observational and cross-sectional prevalence study. 10-18 years aged participants with adolescent idiopathic scoliosis were recruited in the study. Myofascial pain syndrome will be questioned to the participants. additionally, all participants will be evaluated using their findings for scoliosis and myofascial pain syndrome diagnostic criteria. Cobb angle, coronal balance, shoulder and pelvis asymmetry, sagittal spino-pelvic parameters of the spine (cervical lordosis, thoracic kyphosis, lumbar lordosis angles and sagittal vertical axis, sacral slop angle and pelvic incidence) will be measured.

NCT ID: NCT04959591 Completed - Clinical trials for Scoliosis; Adolescence

Use of Intravenous Acetaminophen in Pediatrics Undergoing Spinal Fusion Surgery

Start date: June 1, 2021
Phase: Phase 3
Study type: Interventional

The purpose of this study is to investigate whether perioperative intravenous acetaminophen administration reduces postoperative pain and opioid consumption in adolescents and pediatric patients undergoing spinal fusion surgery.

NCT ID: NCT04822935 Completed - Clinical trials for Scoliosis; Adolescence

Postoperative Pain in Adolescent Idiopathic Scoliosis Surgery

Start date: June 30, 2021
Phase: N/A
Study type: Interventional

Scoliosis is a 3-dimensional, structural deformity of the spine. Idiopathic scoliosis is the most common type and it constitutes 75-80% of all scoliosis. Surgical methods are the most effective way to correct the deformity in patients who cannot achieve adequate improvement with supportive therapy. Adolescent idiopathic scoliosis surgeries are among the most invasive surgeries performed on children and adolescents. Large surgical incision and massive tissue damage cause severe postoperative pain. In this study, we aim to compare posterior instrumentation (PE) and vertebral body tethering (VBT) surgeries performed in adolescent idiopathic scoliosis patients in terms of anesthetic management and postoperative pain.

NCT ID: NCT04403152 Completed - Clinical trials for Scoliosis Idiopathic

Postoperative Rehabilitation or Mobilization After Scoliosis Surgery

Start date: February 5, 2017
Phase: N/A
Study type: Interventional

Scoliosis surgery is a major surgery associated with postoperative pain, loss of physical function and pulmonary dysfunction in adolescent idiopathic scoliosis patients (AIS).Despite the advanced, various medical treatment methods of pain applied in the postoperative period, the mean period of hospitalization is 5 to 7 days. The increasing health expenditures over the years have brought along the need for rehabilitation programs conducted in the early term. Although early mobilization has been accepted as a rule of thumb by spinal surgeons in preventing the performance loss and reducing the causes of morbidity in recent years, the investigators could not find any research on postoperative rehabilitation implemented on patients under the supervision of a physiotherapist, following scoliosis surgery. The aim of this study was to compare effect of five days of intensive postoperative rehabilitation and mobilization on length of hospitalization and outcome in patients having scoliosis surgery.