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Developmental Disabilities clinical trials

View clinical trials related to Developmental Disabilities.

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NCT ID: NCT03067064 Enrolling by invitation - Clinical trials for Child Development Disorder

Prevelance of Molar Incisor Hypomineralization Among a Group of Egyptian Children

MIH
Start date: February 17, 2017
Phase: N/A
Study type: Observational [Patient Registry]

The purpose of this study is to find out the prevalence of molar incisor hypomineralization among a group of Egyptian children

NCT ID: NCT02985749 Completed - Clinical trials for Autism Spectrum Disorder

A Study of Oxytocin for the Treatment of Social Impairment in Individuals With High Functioning Autism Spectrum Disorder

Start date: October 9, 2017
Phase: Phase 3
Study type: Interventional

This study is an 8-week pilot trial with oxytocin nasal spray (Syntocinon) as a treatment for social impairment in children and adults with high functioning autism spectrum disorders (ASD). The investigators hypothesize that oxytocin will be safe, tolerable, and effective in improving social deficits in individuals with ASD.

NCT ID: NCT02930603 Recruiting - Clinical trials for Child Development Disorders

A Longitudinal Study of Function and Participation in Life Activities of Patients With Developmental Disabilities

Start date: April 2014
Phase:
Study type: Observational

A Longitudinal Study of Function and Participation in Life Activities of Patients with Developmental Disabilities

NCT ID: NCT02912065 Completed - Clinical trials for Developmental Disabilities

Tube Feeding Tolerance After Switch to Peptide Based Formula in Children With Developmental Delay

Start date: January 2015
Phase: N/A
Study type: Observational

A retrospective chart review to assess feeding tolerance in children who had been switched from an intact protein formula to a Peptide based formula due to feeding intolerance in a pediatric facility for the developmentally delayed.

NCT ID: NCT02909959 Completed - Clinical trials for Autism Spectrum Disorder

Sulforaphane for the Treatment of Young Men With Autism Spectrum Disorder

Start date: March 1, 2017
Phase: Phase 2
Study type: Interventional

The aim of this randomized controlled trial is to determine if a nutritional supplement containing broccoli sprout and seed extracts, a rich source of sulforaphane, is effective in reducing core symptoms of autism spectrum disorder (ASD). The study will also explore the safety and tolerability of a sulforaphane supplement in young men with ASD, as well as its effects on challenging neuropsychiatric symptoms that are commonly associated with ASD, such as hyperactivity, irritability, and repetitive movements.

NCT ID: NCT02898298 Completed - Clinical trials for Neurodevelopmental Disorders

Positive Emotion Regulation Training in Children, Adolescents and Young Adults With and Without Developmental Disorder

ERICA
Start date: August 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the efficacy of a novel positive emotion regulation intervention that aims to increase positive emotions and improve emotion regulation skills in children, adolescents and young adults. The study focuses on individuals with a developmental disorder such as Autism Spectrum Disorder and other Learning or Developmental Disabilities in comparison to typically developing (TD) controls. Participants will complete a psycho-educative training to learn about positive emotions and how to increase them in their daily lives. Participants are expected to benefit from the training, which will be evident in a change in emotion experience, emotion regulation strategy use, and well-being. Emotion regulation efficacy will be related to symptom severity (autistic symptoms), alexithymia and problematic behaviors.

NCT ID: NCT02803801 Completed - Clinical trials for Autism Spectrum Disorder (ASD)

Build Your Parenting Toolkit: Guiding Children to Become Flexible Thinkers

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

This pilot project is a cooperative effort between the Leisure in Fun Environments (LIFE) Program and the Specialized Communication Resources for Children (SCRC) Program at the Rehabilitation Centre for Children (RCC). The investigators will blend and enhance two pre-existing programs in order to provide a new, specialized program for parents of children with ASD or developmental delay. The two programs that will be blended together are "Promoting Flexible Thinking and Interaction with Your Child at Home" and "Saturday Cooking Club." This new program will be a series of ten workshops that alternates between "parents only" learning sessions and practical "cooking club" sessions that allow parents to focus on practicing what they are learning with their child. These programs are based on the principles of Relationship Development Intervention (RDI®), which focuses on providing opportunities to establish a guided participation relationship, which will lead to development of dynamic intelligence and important social thinking abilities. The program is individualized to each child and builds on the principles of typical development to assist the child in achieving social competence. Using this program, children are expected to develop sociability in a naturally progressing order of complexity.

NCT ID: NCT02797639 Completed - Clinical trials for Mental Retardation and Developmental Disabilities With Organic Condition

Collaborative Consultation for Participation Among Students With IDD

Start date: September 2014
Phase: N/A
Study type: Interventional

Objective: Developing and corroborating the Collaborative Consultation for Participation of Students with Intellectual Disability (Co-PID) program, for enhancing classroom participation among students with moderate Intellectual and Developmental Disability (IDD). Method: study took place in two special education schools and included students with moderate IDD (n=60) and their teachers (n=11). The settings were randomly assigned to intervention or control group. In the intervention group, Co-PID program was employed; in the control group an In-Service (IS) was employed. Participation was evaluated at pre-test and post-test.

NCT ID: NCT02792894 Completed - Clinical trials for Neurodevelopmental Disorders

Family Networks (FaNs) for Children With Developmental Disorders and Delays

FaNs
Start date: April 2016
Phase: N/A
Study type: Interventional

Over 6% of children in Pakistan suffer from a developmental disorder (intellectual disability or Autistic spectrum disorder) and most receive no intervention.In an earlier proof of concept study, the investigators integrated social, technological and business innovations to develop and successfully pilot a sustainable service for such children in one rural population of 30,000. Affected families were identified through a mobile phone-based interactive voice response system, and organised into family networks. 'Champion' family volunteers were trained in evidence-based interventions. A Tablet-based android application was developed for training, monitoring and supervision of the champions, based on the World Health Organization's guidelines. The champions delivered the intervention to other families in the network. The project was sustainable and demonstrated significant improvements in the lives of children and their families in the first 6 months of its operation. The investigators are scaling-up this intervention to a population of 1 million. The investigators aim to evaluate the effectiveness and cost effectiveness of the scaled-up programme using cluster randomized control trial nested within the scale-up study.

NCT ID: NCT02745990 Enrolling by invitation - Clinical trials for Developmental Disabilities

Recombinant Human Erythropoietin Improve Neurodevelopmental Outcomes in Extremely Preterm Infants

EPO
Start date: May 2016
Phase: N/A
Study type: Interventional

In the ELGAN (Extremely Low Gestational Age Newborn) study, abnormal brain structure and function were associated with intermittent or sustained systemic inflammation (ISSI). Since EPO has anti-inflammatory properties in the kidney and in muscle as well as growth/trophic properties. Based on its potential for neuroprotection, the prospective randomized and masked study was designed to determine whether rhEPO (500u/kg) was also effective in improving developmental outcomes for extremely low gestational age newborns.