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临床试验/NCT00419432
NCT00419432Unknown不适用

Functional Outcomes Following Orthopaedic Surgery Based on Gait Laboratory Versus Observational Gait Analysis in Ambulatory Children With Cerebral Palsy: A Multi-center Randomized Controlled Trial.

The Hospital for Sick Children10 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2007年1月最近更新:
适应症

试验速览

阶段
不适用
入组人数
60
试验地点
10
主要终点
General Effect Size of Secondary Outcomes

研究概览

简要总结

The purpose of this pilot trial is to determine whether the addition of gait laboratory analysis for surgical decision making, compared with the use of observational analysis alone, results in improved functional outcomes in ambulatory children with cerebral palsy undergoing multi-level lower extremity orthopaedic surgery.

详细描述

Children with cerebral palsy, who are ambulatory, have an inefficient gait often associated with functional disability. Many of these children are candidates for orthopaedic surgery, which includes multi-level soft tissue and bony procedures. Pre-operative planning is based on the physical examination and visual (observational) analysis of the child's gait. In some centres, patients undergo additional gait analysis in a motion laboratory. While gait laboratory analysis is accepted as an important research tool, there is controversy about its clinical utility in decision making for the surgical management of this population. To date, no clinical trials have been undertaken to answer this question, and the appropriate clinical utilization of this technology is yet to be established. The consequence of this uncertainty is that ambulatory children with cerebral palsy are either being deprived of a useful assessment tool in some centres, or alternatively they are being subjected to an unnecessary evaluation that is both expensive and time consuming in other centres. A multi-centre randomized trial will provide evidence to support or refute the need for gait laboratory analysis for surgical decision-making for this population. This pilot randomized controlled trial in four sites will assess the feasibility of, and provide the template for the design and conduct of the definitive larger multi-centred trial to extend its generalizability across North America and other jurisdictions. The specific objectives include:

  1. Establish the feasibility of implementing the randomized trial study design in multiple centres
  2. Estimate recruitment rates and timelines
  3. Establish responsiveness of outcome measures to finalize the primary & secondary outcomes
  4. Estimate effect sizes of functional outcomes for sample size calculations
  5. Establish data management system (web-based database) for definitive multi-centre study.
  6. Assess feasibility, reliability and face validity of pilot health economic data forms to include health economic evaluation in the future definitive multi-centre trial.

Secondary objectives include: 7. Does the addition of gait analysis alter surgical decisions made from video observation alone, when performed in the setting of this pilot trial? 8. Evaluate the consistency of the surgical decision making: intra- & inter rater reliability

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
Double (Participant, Care Provider)

入排标准

年龄范围
6 Years 至 15 Years(Child)
性别
All
接受健康志愿者

入选标准

  • Diagnosis of spastic cerebral palsy.
  • Age 6 to 15 years at the time of the initial assessment.
  • Gross Motor Function Classification System (GMFCS) levels II or III (demonstrable independent ambulatory potential with or without orthotics/assist devices).
  • Patients have been referred for assessment and treatment of gait abnormality.
  • Patients have a gait abnormality interfering with their physical function.
  • Patients are candidates for orthopaedic surgery including soft tissue and/or bony procedures involving at least 2 levels, in one or both lower extremities (e.g. knee & ankle).
  • Patients must be able to undergo instrumented gait analysis in a motion laboratory.

排除标准

  • Presence of dystonia, athetosis, or mixed tone abnormalities.
  • History of orthopaedic lower extremity procedures within the previous 2 years.
  • Patients who have had previous gait laboratory analysis that has been seen by the treating surgeon.
  • Patients who will be unable to return for the required follow up visits/gait analysis.

结局指标

主要结局

General Effect Size of Secondary Outcomes

时间窗: Post Study

The final primary and secondary outcome measures will be chosen based on responsiveness and their effect sizes used to calculate sample size for a future definitive trial.

次要结局

  • Gait Parameters(Baseline, 12-, 24-months follow-up)
  • Gross Motor Function Measure (GMFM-66)(Baseline, 6, 12, 24 months follow up)
  • Pediatric Outcomes Data Collection Instrument(PODCI)(Baseline, 6, 12, 24 months follow up)
  • Functional Mobility Scale (FMS)(Baseline, 6, 12, 24 months follow up)
  • Activity Scale for Kids (ASK)(Baseline, 6, 12, 24 months follow up)
  • Gillette Functional Assessment Questionnaire (FAQ)(Baseline, 6, 12, 24 months follow up)
  • Gillette Gait (Normalcy) Index (GGI)(Baseline, 6, 12, 24 months follow up)

研究者

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

Unni Narayanan

Orthopaedic Surgeon

The Hospital for Sick Children

研究点 (10)

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