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Spina Bifida clinical trials

View clinical trials related to Spina Bifida.

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NCT ID: NCT03851107 Completed - Cerebral Palsy Clinical Trials

The Effectiveness of Participation-focused Interventions on Body Functions of Youth With Physical Disabilities

Start date: September 1, 2017
Phase: N/A
Study type: Interventional

Youth with physical disabilities face greater restrictions to participation in community-based activities than their typically developing peers, which can lead to poor health outcomes. Emerging treatment approaches aimed at improving activity and participation have shifted from focusing only on impaired body functions towards the performance of functionally meaningful activities within the youth's natural environment. It is unclear, however, whether targeting intervention at the activity/participation level can, at the same time, result in improvement of personal functional skills (e.g., reaching) and body functions (e.g., range of motion) -components also important to address and maintain within the rehabilitation process. Together with key community-based stakeholders including youth/parents, clinicians, and policy-makers, the investigators plan, therefore, to examine whether engaging in a 6-week community based activity (e.g., joining a sledge hockey team, boccia) can lead to a significant improvement in three key body functions: motor, cognitive and affective functions. Eight participants with physical disabilities will take part in the study and engage in an activity program of their own choice. Changes in their body functions (e.g., movement-related functions, attention, behavior, mood) will be measured multiple times before, during and after the engagement in an individualized activity/program. Findings of this pilot study analyzed with input from key stakeholders can advance the investigators understanding about methods for testing complex and unique individual-based interventions. This can guide clinicians, families and policy-makers to select effective approaches that not only promote participation but can also facilitate additional (motor and mental) benefits from one single intervention. Such findings may also reduce the burdens on the healthcare system as well as on the youth and families.

NCT ID: NCT03573726 Completed - Neurogenic Bladder Clinical Trials

Use of a Diurnal Indwelling Urethral Catheter to Improve Quality of Life

Start date: September 11, 2013
Phase: N/A
Study type: Interventional

This is an interventional study examining the effects of closed diurnal indwelling catheterization (CDIC) for neurogenic bladder management.

NCT ID: NCT03543995 Completed - Spina Bifida Clinical Trials

The Relationship Between Nocturnal Enuresis And Spina Bifida Occulta

Start date: January 1, 2017
Phase:
Study type: Observational [Patient Registry]

It is claimed that SBO may be responsible for bladder dysfunction in patients without known neurological disease. Subsequently, it was reported that the frequency of SBO in NE cases was higher than normal children. However, in controlled trials, SBO frequency was not different in NE patients compared to the normal population. Conversely, the incidence of dysfunctional bladder in the presence of SBO in NE patients was found to be higher and the response to treatment was worse than in non-SBO patients. The present study aimed to determine whether the frequency of SBO in patients with NE was higher than in healthy subjects, the effect of SBO on the severity of LUTS and whether treatment response of primary NE patients changed in the presence of SBO.

NCT ID: NCT03466996 Completed - Spina Bifida Clinical Trials

Telemedicine in Spina Bifida Transition: A Pilot Study

Start date: June 1, 2018
Phase: N/A
Study type: Interventional

The purpose of this study is to explore the feasibility and efficacy of using telemedicine to improve transition from pediatric to adult care in patients with spina bifida.

NCT ID: NCT03135145 Completed - Cerebral Palsy Clinical Trials

Post-operative Lite Run Study

Start date: May 15, 2017
Phase: N/A
Study type: Interventional

Lite Run is a new assistive device that may have FDA listing as a Class I device by mid 2017 based on clinical testing of adults, independent agency testing and in-house evaluations. This will be a combined study with multiple purposes with respect to the evaluation of its use with the post-operative pediatric population. A first purpose is to verify safety and feasibility of the device on pediatric patients. A second purpose is to statistically test the effectiveness of Lite Run to decrease physical burden on the therapist during post-operative gait training for children and adolescents with cerebral palsy as compared to current methods of body weight-supported gait training. A third purpose is to measure and qualitatively evaluate the effectiveness of the device on patient outcomes and improving patient and therapist satisfaction.

NCT ID: NCT03121651 Completed - Cerebral Palsy Clinical Trials

Medication Management Among Individuals With Neurodevelopmental Disabilities

M-MIND
Start date: November 11, 2016
Phase: N/A
Study type: Interventional

This is a pilot study to develop a reinforcement learning (RL)-adaptive visual and interactive support application (hereafter RL-adaptive support) to help young adults with spina bifida or cerebral palsy become more independent with medication management. Individuals with disabilities who are empowered to manage several aspects of their lives can ultimately be better integrated into and contribute more to society.

NCT ID: NCT03045276 Completed - Kidney Transplant Clinical Trials

Urological and Renal Disease Engaging Adolescents in Adherence Collaborative Trial

U-REAACT
Start date: June 29, 2017
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the effectiveness of behavioral feedback plus economic incentives to promote treatment adherence among a large diverse population of adolescents and young adults (AYA) with kidney transplant (KT) or spina bifida (SB).

NCT ID: NCT02854150 Completed - Spina Bifida Clinical Trials

Improving Genetic Counseling for Patients With Spina Bifida Using Next Generation Sequencing

EXOSPINA
Start date: September 2015
Phase:
Study type: Observational

The main objective is to improve genetic counseling in patients with Spina Bifida, by the characterization of variants in new genes using high throughput sequencing either on a panel of targeted genes or on exome in families.

NCT ID: NCT02852317 Completed - Multiple Sclerosis Clinical Trials

Urinary Markers of Detrusor Overactivity in Spina Bifida Patients

BUHD-SPINA
Start date: March 16, 2015
Phase:
Study type: Observational

The purpose of this study is to assess diagnostic performance of urinary markers of detrusor overactivity (Nerve Growth Factor (NGF), Brain-Derived Neurotrophic Factor (BDNF), adenosine triphosphate (ATP), Prostaglandine E2) in detected high pressure bladder un spina bifida patients.

NCT ID: NCT02682043 Completed - Children Clinical Trials

Parental Perspectives of Using Toy Cars on Social Interactions of Preschool Children With Mobility Impairments

Start date: February 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate parental attitudes towards their child who has a mobility impairment, to using a modified electric toy car, and to evaluate from their perspective, if it facilitated social interaction for their child with mobility impairment.