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Spinal Dysraphism clinical trials

View clinical trials related to Spinal Dysraphism.

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NCT ID: NCT00951509 Completed - Spinal Cord Injury Clinical Trials

Virtual Reality Based Testing of Power Wheelchair Driving Skills

Start date: August 2011
Phase: N/A
Study type: Observational

The purpose of this research study is to examine whether computer based or virtual reality based driving assessments are as useful as real-world power wheelchair driving tests in measuring driving performance and whether they may be useful in helping to identify the problems that some individuals may have with driving power wheelchairs. The specific aims are as follows: Specific Aim 1: To develop computer-based and VR-based wheelchair driving assessments for both drivers and non-drivers that correspond to an accepted real-world driving assessment (Power Mobility Road Test) and compare them to the real-world assessment and to each other. Specific Aim 2: To develop additional features of the computer-based and VR-based assessments that present dynamic tasks and determine whether skills on these tasks can be delineated within the virtual environment.

NCT ID: NCT00891891 Active, not recruiting - Spina Bifida Clinical Trials

Psychosocial Adjustment of Adolescents With Spina Bifida

CHATS
Start date: September 2005
Phase:
Study type: Observational

The purpose of this longitudinal study is to evaluate a developmentally-oriented bio-neuropsychological model of adjustment in youth and young adults with spina bifida. The theoretical framework for the study is a developmentally-oriented bio-neuropsychosocial model of psychological adjustment.

NCT ID: NCT00866112 Completed - Stroke Clinical Trials

A Randomized Exercise Trial for Wheelchair Users

Start date: May 2008
Phase: N/A
Study type: Interventional

People with mobility disabilities are at greater risk than the general population for incurring health problems. Many of these conditions are preventable through behavior and lifestyle changes such as exercise and physical activity. Recent evidence suggests that people with disabilities experience the same physiologic response to exercise as the general population. Nonetheless, nearly three-fourths of those with disabilities report being entirely sedentary or not active enough to achieve health benefits. Despite some knowledge of issues that limit physical activity among this population, few studies have investigated methods for promoting physical activity adoption among people with disabilities, including wheelchair users. The purpose of this study is to test the effectiveness of a behavioral intervention to promote physical activity adoption over 6 months and maintenance of physical activity over another 6 months by community-dwelling manual wheelchair users.

NCT ID: NCT00767988 Withdrawn - Clinical trials for Urinary Tract Infection

Probiotics in Girls With Spina Bifida

Start date: n/a
Phase: Phase 2
Study type: Interventional

Girls with spina bifida also have bladder problems. This is because they need temporary placement of a tube into the bladder to remove urine. This thin flexible tube is called a catheter. It can increase the risk of having bacteria in the urine. This in turn can lead to urinary tract infection (UTI). Some girls with spina bifida are given antibiotics. These are medicines used to treat infections caused by bacteria. The medicine is used to prevent UTI. However, long-term treatment with these medicines can have side effects. For example, the bacteria may become resistant to the antibiotics. Also, bacteria in the urine can persist. UTI can still occur in patients on antibiotics. UTI in girls occurs because bacteria migrate from the rectum to the vagina area. This gives the bacteria access to the bladder. Also, in girls with spina bifida, the access to the bladder is easier because of the catheter. Probiotics are friendly bacteria. They are available as dietary supplements and as food. They contain helpful bacteria. Yogurt is an example of a food that contains probiotics. The purpose of this study is to find out, if probiotics taken for 6 months can prevent UTI in girls with spina bifida. We will also try to find out whether changes in urine bacteria are associated with the taking of the probiotics. A vaginal and rectal swab will also be done to find out if taking probiotics has any benefits on preventing bacteria.

NCT ID: NCT00720161 Completed - Clinical trials for Neuromuscular Diseases

Metformin in Children With Motor Deficit

Start date: November 2006
Phase: N/A
Study type: Interventional

Obesity with insulin resistance in the paediatric population provides an increasing challenge. Children with neurological or neuromuscular diseases are even more prone to obesity: their locomotor impairment leads to an increasingly sedentary lifestyle, a decrease in physical fitness and an increase in body fat (1-3). Obesity, in turn, can be associated with a decrease in physical fitness and a further increase in body fat. In this study we want to evaluate the effect of an insulin-sensitizer, metformin, in a group of overweight/obese patients with neurological or neuromuscular diseases. Metformin is a well-established insulin sensitizer.

NCT ID: NCT00655681 Completed - Cerebral Palsy Clinical Trials

Prevention of Post Operative Bone Loss in Children

Start date: September 2007
Phase: N/A
Study type: Interventional

Hypothesis: one-dose pamidronate will prevent post-operative bone loss in children at risk for low bone density Plan: children with chronic disease such as CP, spina bifida, etc. will be recruited pre operatively and studied with DXA scan. After surgery, children will be randomized to receive either pamidronate or saline. Repeat DXA scan will determine bone lost after end of immobilization or nonweightbearing.

NCT ID: NCT00468481 Completed - Contraception Clinical Trials

Efficacy and Safety Study for an Oral Contraceptive Containing Folate

Start date: April 2007
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine whether the study drug is safe and effective

NCT ID: NCT00452829 Completed - Clinical trials for Recurrent Neural Tube Defects

Prevention of Neural Tube Defects by Inositol in Conjunction With Folic Acid (PONTI Study)

Start date: September 2009
Phase: Phase 1
Study type: Interventional

The aim of the study is to develop a randomised, double blind clinical trial to compare (i) folic acid plus inositol, with (ii) folic acid plus placebo, for prevention of recurrent neural tube defects.

NCT ID: NCT00394862 Completed - Neural Tube Defects Clinical Trials

Efficacy of Weekly Versus Daily Folic Acid Supplementation

Start date: January 2006
Phase: N/A
Study type: Interventional

Investigate the efficacy of weekly versus daily of folic acid supplementation on improving folate, vitamin B12,

NCT ID: NCT00378664 Completed - Clinical trials for Urinary Incontinence

Lumbar to Sacral Ventral Nerve Re-Routing

Start date: September 2006
Phase: Phase 2
Study type: Interventional

To assess the level of improvement in voiding function after lumbar to sacral ventral nerve re-routing procedure in Spinal Cord Injury and spina bifida patients