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临床试验/NCT00467415
NCT00467415Unknown不适用

Multi-Center Project: Supported Speed Treadmill Training Exercise Program (SSTTEP) for Marginally Ambulatory Children With Cerebral Palsy

Shriners Hospitals for Children6 个研究点 分布在 1 个国家目标入组 66 人开始时间: 2007年5月最近更新:
适应症

试验速览

阶段
不适用
入组人数
66
试验地点
6
主要终点
Canadian Occupational Performance Measure (COPM)

研究概览

简要总结

The investigators are studying the effects of a 12-week exercise program, consisting of either:

  1. Walking on a treadmill with partial body weight
  2. Functional exercise program

The investigators would like to know the effects these two exercise programs have on the quality of life, muscle strength and control, coordination, walking, and functional movement of children with cerebral palsy who are marginal ambulators. This is a randomized control trial with subjects randomly assigned to one of the 2 groups.Subjects in both groups will be seen twice a day for two weeks at our hospital for intervention and parent training, and then participate in a 10 week home-based program. During each subject's two-week clinic-based training, a parent or caregiver is trained in all home program exercises and/or equipment usage. This person must be able to safely perform the exercise program with the child. Each subject will also need to participate in three separate 5-hour long data collection sessions scheduled over the 4 month study period.

详细描述

This project proposes to answer the following questions: Is partial body weight supported treadmill gait training (PBWSTT) effective in improving ambulation abilities, neuromuscular impairments, functional mobility, disability, and quality of life in marginally ambulatory children with cerebral palsy.

Specific Aim 1: Assess the effect of a PBWSTT locomotor training intervention on quality of life, treatment expectations, self-efficacy, and activity and participation of children with CP with limited ambulation skills. We hypothesize that in comparison to a control group, after a 12 week locomotor intervention, children with CP (intervention group) with limited ambulation skills will demonstrate greater improvements in scores from common questionnaires compared to the control group.

Specific Aim 2: Assess the effect of a PBWSTT locomotor training intervention on gross motor skills; physical function; biomechanics and coordination dynamics of ambulation; and physical activity in ambulatory children with CP. We hypothesize that in comparison to a control group, after a 12 week PBWSTT locomotor training intervention children with CP with limited ambulation skills will demonstrate greater improvements in functional test scores compared to the control group.

Specific Aim 3: Assess the effect of a PBWSTT locomotor training intervention on measures of body structure and function including: spasticity; muscle strength; and joint-specific motor control. We hypothesize that in comparison to a control group, after a 12 week PBWSTT locomotor training intervention children with CP with limited ambulation skills will demonstrate greater improvements in: muscle strength, spasticity and joint specific motor control compared to the control group.

This is a single blinded, randomized, controlled pre-test/post-test study design. Sixty six ambulatory children between the ages of 6-12 years of age with cerebral palsy will undergo a 12-week training program. Thirty three of these children will undergo a Supported Speed Treadmill Training Exercise Program (SSTTEP), and the remaining 33 children will receive the same amount of conventional physical therapy in the form of a personalized home exercise program and serve as a control group. Three sets of measures will be obtained: A1) at baseline prior to intervention; A2) at the end of the 12-week intervention period; and A3) 4 weeks after the intervention has ended.

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
Single (Outcomes Assessor)

入排标准

年龄范围
6 Years 至 13 Years(Child)
性别
All
接受健康志愿者

入选标准

  • A diagnosis of spastic cerebral palsy;
  • Impaired ambulation abilities as evidenced by a decreased in gait velocity below 80% of age expected value or gross motor function classification scale (GMFCS) Level III or IV;
  • Able to ambulate independently for 8 steps with/without assistive devices to allow for adequate motion analysis data collection;
  • Body weight of less than 150 pounds;
  • Between the ages of 6 and 13 years;
  • Able to follow multiple step commands and to attend to tasks associated with data collection;
  • Willingness to travel to one of the three sites for data collection sessions, and 2 weeks of intensive intervention;
  • Willingness to commit to home program 30 minutes per session, 5 times week for 10 weeks, as well as adequate space and supervision for treadmill use at home;
  • No reported musculoskeletal, cardiovascular or pulmonary conditions that would limit participation in moderate exercise program;
  • Minimum of 12 months post surgery including soft tissue releases
  • Six months post-Botox injections, significant changes in Baclofen dosing, or casting procedures to the lower extremities;
  • Passive range of motion of lower extremity joints: < 30º contracture of hip in extension as measured by the Thomas Test; passive dorsiflexion range of motion to -15º with the knee extended, and knee extension range (90º/90º test) to 70º and <-20º knee extension.
  • At least 2 years post- dorsal rhizotomy.

排除标准

  • Children with "mixed" types of CP (i.e. athetosis) or other movement disorders (e.g. ataxia);
  • Children receiving intrathecal Baclofen (baclofen pump);

结局指标

主要结局

Canadian Occupational Performance Measure (COPM)

时间窗: 6 months

Gait Velocity

时间窗: 6 months

Muscle Activation and Timing

时间窗: 6 months

Piers-Harris Children's Self-Concept Scale, 2nd Edition (PHCSCS-2)

时间窗: 6 months

Gross Motor Function Measure (GMFM)

时间窗: 6 months

Pediatric Outcomes Data Collection Instrument (PODCI)

时间窗: 6 months

Gait Spatio-Temporal Parameters

时间窗: 6 months

Pediatric Quality of Life Inventory (PEDS-QL)

时间窗: 6 months

Children's Assessment of Participation and Enjoyment (CAPE)

时间窗: 6 months

次要结局

未报告次要终点

研究者

申办方类型
Other

研究点 (6)

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