Preoperative and postoperative clinical efficacy of PSSE in perioperative AIS patients

Preoperative and postoperative clinical efficacy of PSSE in perioperative AIS patients - Clinical effect of PSSE on perioperative AIS patients before and after surgery

Status

Active, not recruiting

Phases

Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2300070979

Enrollment

Unknown

Registered

2023-04-27

Start date

2023-05-01

Completion date

Unknown

Last updated

2023-06-04

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

Conditions

Adolescent Idiopathic Scoliosis

Interventions

Experimental group:Physiotherapeutic scoliosis specific exercises,PSSE

Control group:Core strength training

Eligibility

Sex/Gender

All

Age

10 Years to 18 Years

Inclusion criteria

Inclusion criteria: ? Patients diagnosed with adolescent idiopathic scoliosis ? The age range is 10-18 years old ? Patients undergoing posterior selective thoracic fusion ? Patients with follow-up longer than 6 months

Exclusion criteria

Exclusion criteria: 1. Patients diagnosed with non-idiopathic scoliosis (congenital scoliosis, postural scoliosis, neuromuscular scoliosis, compensatory scoliosis, etc.); 2. Patients with diseases that prevent them from exercising; 3. Patients with other cardiopulmonary diseases or dysfunction; 4. Patients with significant cognitive deficits who could not complete the SRS-22 questionnaire

Design outcomes

Primary

Measure	Time frame
Psychological status and quality of life assessment;	—

Secondary

Measure	Time frame
Lung function;Cobb Angle;Symmetry ratio of concave-convex paravertebral muscle;	—

Countries

China

Contacts

Public ContactMeng Fanyuan

Kunming Medical University

1273153146@qq.com+86 15096634903

Outcome results

None listed

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