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Down's Syndrome clinical trials

View clinical trials related to Down's Syndrome.

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NCT ID: NCT06176755 Completed - Down's Syndrome Clinical Trials

Treadmill Training With and Without Weighted Ankle Cuffs on Gait Parameters

Start date: October 26, 2023
Phase: N/A
Study type: Interventional

Down syndrome is a condition in which a person has an extra chromosome. Chromosomes are small "packages" of genes in the body. Down syndrome (DS), also known as trisomy 21, is caused by the presence of all or part of a third copy of chromosome 21. It is named after John Langdon Down, the British physician who described the syndrome for the first time in 1866.Down syndrome remains the most common chromosomal condition diagnosed in the United States. Current study will be randomized controlled trial. Study will be approved by ethical committee. After that informed consent will be taken and patients will be included in the study based on the inclusion criteria. Sampling technique will be simple random sampling the calculated sample sizes will be 25 in each group. All participants will be divided in two groups. One group will receive treadmill training with Weighted Ankle Cuffs and second group will receive treadmill training only. Conventional therapy will be given to both groups which include isometric, strengthening exercise and trunk exercise. The exercise was given for 10 repetitions/session. Infants will receive the treadmill training protocol about 6 min/day, 4 day/week at a belt speed of 0.18m/sec. After taking informed consent baseline measurement will be taken through gait assessment rating scale and Berg balance scale for balance and Gait parameters respectively. Data will be collected before treatment and after 6 weeks. Treatment session will be performed for 1 hour per day, 4 days a week for total of 6 weeks. The difference in improvement before and after 4th weeks will be noted and compared through SPSS 26.0.

NCT ID: NCT05392322 Recruiting - Down's Syndrome Clinical Trials

Effect of Virtual Video Reality Gaming on Fine Motor Skills in Children With Down's Syndrome

Start date: October 25, 2021
Phase: N/A
Study type: Interventional

Down's syndrome is genetic disorder caused by trisomy 21. Children with Down's syndrome are characterized by awkward movements, gait, increased flexibility of joints, timing of mastering of basic skills, under development of fine motor skills. Virtual Reality Therapy (VRT) is a technique that uses interactive games as a physical therapy resource and has shown positive results in cortical reorganization, improving functional mobility, and quality of movement. This is an experimental study in which randomized controlled trials study design is being used.

NCT ID: NCT01794013 Completed - Cerebral Palsy Clinical Trials

DIR/ Floortime™ Parent Training Intervention for the Children With Developmental Disabilities

RCT/DD
Start date: March 2013
Phase: N/A
Study type: Interventional

The objective of this study is to test whether adding the parent training program using the relationship-based approach could help the children with development disabilities (DDs) would confer additional benefits over routine clinical care available to both groups in terms of improving their development and reducing behavior problems.

NCT ID: NCT01758718 Completed - Down's Syndrome Clinical Trials

Eyelash Line Resection for Entropion Associated With Down's Syndrome

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

Surgical outcome of entropion associated with Down's syndrome was evaluated. Grading scale of superficial punctate keratopathy and score of wearing glasses to correct refractive errors were measured.

NCT ID: NCT01379443 Completed - Cerebral Palsy Clinical Trials

Rehabilitation of Children With Multiple Disabilities

Start date: April 2007
Phase: Phase 1
Study type: Interventional

The objective of the study is to compare the usual care and treatment of children and youth (0-19 years) with multiple developmental delays and disabilities and their families in Simcoe York with a co-ordinated, navigated approach to care using the Children's Treatment Network (CTN) services.

NCT ID: NCT00240760 Recruiting - Dementia Clinical Trials

Memantine and Down's Syndrome

Start date: October 2005
Phase: N/A
Study type: Interventional

This is a study to assess whether memantine is effective and safe in preventing age related cognitive deterioration and dementia in people with Down's syndrome (DS) age 40 and over. The study will last for a year and it will include 180 people with Down's syndrome with and without dementia. Participants will be assessed on memory skills, attention and problem solving abilities. Quality of life and abilities for everyday living skills will also be regularly checked. Primary Aims Clinical: - To determine the clinical efficacy of memantine versus placebo in preventing cognitive decline in people with DS. - To compare the safety and tolerability of memantine versus placebo in people with Down’s syndrome (DS). Biochemical and pathological: - To examine the ability of memantine to alter markers of disease progression in DS patients. Secondary Aims Clinical: - To determine whether memantine has, as compared with placebo, a significant positive impact on: - level of independent functioning as measured by the carer-rated adaptive behavioural scale, (ABS) in adults with DS; - quality of life in adults with DS. Biochemical and pathological: - To investigate putative markers of memantine’s mechanism of action in peripheral samples from living patients with DS.

NCT ID: NCT00001178 Terminated - Dementia Clinical Trials

Brain Study of Patients With Frontal Lobe Dementia and Parkinsonian Disorders

Start date: January 19, 1981
Phase:
Study type: Observational

The Cognitive Neuroscience Section of the National Institute of Neurological Disorders and Stroke proposes to continue its cross-sectional and longitudinal studies of cerebral metabolism in frontal lobe dementias and atypical basal ganglia disorders. These studies include repeated assessments of neuropsychological and brain anatomical and metabolic function in subjects with these important and possibly related brain disorders.