Motion Analysis of Sit-to-Stand Movements in Children With Spastic Diplegia

The recruitment status of this study is unknown because the information has not been verified recently.
Verified April 2006 by Far Eastern Memorial Hospital.
Recruitment status was  Not yet recruiting
Sponsor:
Collaborator:
National Taiwan University
Information provided by:
Far Eastern Memorial Hospital
ClinicalTrials.gov Identifier:
NCT00314301
First received: April 12, 2006
Last updated: April 14, 2006
Last verified: April 2006
  Purpose

The purpose of this study is to compare movement variations before and after the loaded training, with kinematics, kinetics, and electromyography, in children with spastic diplegia and to further discuss mechanisms of the loaded training.


Condition Intervention
Cerebral Palsy
Device: loaded sit-to-stand training

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Crossover Assignment
Masking: Open Label
Primary Purpose: Educational/Counseling/Training
Official Title: Motion Analysis of Sit-to-Stand Movements in Children With Spastic Diplegia Before and After Loaded Sit-to-Stand Training

Resource links provided by NLM:


Further study details as provided by Far Eastern Memorial Hospital:

Primary Outcome Measures:
  • kinematic measures of lower extremity and the whole body
  • kinetic measures of lower extremity and the whole body
  • electromyographic measures of lower extremity and the whole body

Estimated Enrollment: 20
Study Start Date: April 2006
Estimated Study Completion Date: September 2007
Detailed Description:

Subjects: This study will recruit twenty children who are aged between 5 and 12 years, with spastic diplegia, and without having major surgeries or botulinum toxin injection on lower extremities during the past 6 months prior to participate in this study.

Methods: The Vicon 250 motion analysis system, 3 AMTI force platforms and the EMG recording system will be used to collect data of sit-to-stand (STS) movements. Baseline, pre- and post-training evaluations will be carried out. The duration of the baseline and pre-training evaluations is 2 months. The training period will take about 6 weeks. Each evaluation will take two separate days to accomplish. On the first day, the STS1RM of individual children was determined. On the second day, kinematic and kinetic data of STS movements in natural and loaded (applying load of 50% STS1RM during STS movements) conditions were collected. Data of smoothness, maximal extension moment and around hip and knee joints, onset time of lower extremity muscles will then be calculated. Results of each evaluation will be used for further comparison.

  Eligibility

Ages Eligible for Study:   5 Years to 12 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Diagnosed as spastic diplegia
  • Aged between 5 and 12 years
  • Able to perform the STS movements without assistance
  • Able to cooperate and understand commands given

Exclusion Criteria:

  • Severe musculoskeletal deformity or pain on lower extremities
  • Botulism injection in the past 3 months or major operations in the preceding 6 months on lower extremities
  • Uncontrolled epilepsy
  • Major sensory deficits, such as blindness or deafness
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00314301

Contacts
Contact: Yuh-Ting Lin, MSc 866-2-8966-7000 ext 1411 yuh_ting_lin@hotmail.com
Contact: Jao-Shwann Liang, MD 866-2-8966-7000 ext 1411

Locations
Taiwan
National Taiwan University Hospital Not yet recruiting
Taipei, Taiwan, 100
Contact: Hua-Fang Liao, MPH    886-2-3322\8136    hfliao@ntu.edu.tw   
Principal Investigator: Yuh-Ting Lin, MSc         
Sponsors and Collaborators
Far Eastern Memorial Hospital
National Taiwan University
Investigators
Principal Investigator: Yuh-Ting Lin, MSc Research Ethics Review Committee of the Far Eastern Memorial Hospital
  More Information

No publications provided

ClinicalTrials.gov Identifier: NCT00314301     History of Changes
Other Study ID Numbers: 94023
Study First Received: April 12, 2006
Last Updated: April 14, 2006
Health Authority: Taiwan: Department of Health

Keywords provided by Far Eastern Memorial Hospital:
cerebral palsy
resistance
movement
biomechanics

Additional relevant MeSH terms:
Cerebral Palsy
Brain Damage, Chronic
Brain Diseases
Central Nervous System Diseases
Nervous System Diseases

ClinicalTrials.gov processed this record on August 26, 2014