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临床试验/NCT02807545
NCT02807545已完成不适用

Scoliosis-Specific Exercises for At-Risk Mild Adolescent Idiopathic Scoliosis Curves: A Multi-Site Preliminary Randomized Trial

Texas Scottish Rite Hospital for Children11 个研究点 分布在 1 个国家目标入组 98 人开始时间: 2016年8月2日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
98
试验地点
11
主要终点
Overall Recruitment Rate

研究概览

简要总结

This study will be a multi-center, dual-arm randomized control study evaluating skeletally immature patients with mild AIS curves. At six institutions, patients will be randomized into either the scoliosis-specific exercise (SSE) treatment arm or a control group. The SSE group will receive training in SSE, posture, and activities of daily living by physical therapists certified in Schroth-based exercise methods. The control group will not receive SSE instruction and will only be observed by their treating orthopaedic surgeon (which is considered the standard-of-care treatment method). Results will be compared after one year of treatment.

详细描述

All patients with AIS meeting the following inclusion criteria will be eligible to participate in this trial: diagnosis of AIS; ages 10 to 17 years; major curve Cobb angles 15° to 20°; thoracolumbar, lumbar, or primary thoracic curve patterns; and Risser grade 0. Curves less than 15° will not be as clinically meaningful if they do not progress more than 5°. Curves 15° also allow for 5° of measurement error. Curves more than 20° will not be able to progress at least 5° before bracing is initiated according to SRS criteria (at 25°). Patients will be excluded according to the following exclusion criteria: scoliosis other than AIS, upper thoracic or double curve patterns, developmental disorders that prevent understanding and compliance with an exercise schedule, current or previous brace wear, and previous participation in a SSE program, previous spine surgery, inability to commit to performing a home exercise program for 15 minutes a day, 5 days a week, and inability to commit to attend at least 8 hours of PT within 6 months.

Patient medical records will be reviewed for eligibility. If a patient is deemed eligible for inclusion in the study, a member of the research team will meet with the patient and his or her family to review the consent form in a private medical exam room. The family will be given ample time to review the consent form and ask any questions. If a participant chooses to participate, a consent form will be signed by both the patient and the legal guardian prior to any investigational procedures occurring. Once a consent form has been signed, patients will be randomly assigned by the TSRH on site statistician to one of the two following groups:

  1. Standardization of Physical Therapy:

Physical therapists from Texas Scottish Rite Hospital, Boston Children's Hospital, Columbia University Medical Center, Norton Leatherman Spine Center, Johns Hopkins University, and Texas Children's Hospital who received training and certification in the Schroth-based (BSPTS) method have been recruited as members of the study team. Physical therapists at each institution will deliver a standardized exercise intervention. 2. Study Groups:

A) Scoliosis-Specific Exercise (SSE) Group

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
10 Years 至 17 Years(Child)
性别
All
接受健康志愿者

入选标准

  • All patients diagnosed with Adolescent Idiopathic Scoliosis who meet the following inclusion criteria will be eligible to participate in this trial:
  • Age 10 to 17 years
  • Major curve Cobb angles of 12° to 24°
  • Risser Grade 0
  • Single thoracic, thoracolumbar, or lumbar curve patterns

排除标准

  • Patients will be excluded according to the following exclusion criteria:
  • Scoliosis other than AIS (congenital, neuromuscular, etc)
  • Upper thoracic or double curve patterns
  • Diagnosis of a developmental disorder that prevents understanding and compliance with an exercise schedule
  • Current or previous brace wear
  • Previous participation in a SSE program
  • Previous spine surgery
  • Patient inability to commit to attend at least 8 hours of PT within 6 months

结局指标

主要结局

Overall Recruitment Rate

时间窗: through study completion up to 45 months

Measured by the number of participants enrolled through study completion.

Treatment Attendance in the SSE Group

时间窗: after 1 year

Measured by the number of prescribed hours of physical therapy sessions attended after 1 year

Home Exercise Adherence in the SSE Group According to Weekly E-mails

时间窗: 1 year

Measured by the percentage of prescribed exercises completed from baseline to 1 year

次要结局

  • Curve Magnitude(1 year)
  • Curve Progression(after 1 year)
  • Brace Prescription(after 1 year)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Karina Zapata, PT, DPT, PhD

Principal Investigator

Texas Scottish Rite Hospital for Children

研究点 (11)

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