Clinical Trials Logo

Cerebral Palsy clinical trials

View clinical trials related to Cerebral Palsy.

Filter by:

NCT ID: NCT06269835 Recruiting - Cerebral Palsy Clinical Trials

Intermittent Multifunctional Nutrition Tube in Cerebral Palsy and Dysphagia

Start date: February 28, 2024
Phase: N/A
Study type: Interventional

This was a randomized controlled study including 80 infants with cerebral palsy and dysphagia. The Participants were evenly divided into the observation group (with intermittent oro-esophageal tube feeding, n=40) and the control group (with persistent nasogastric tube feeding , n=40). Nutritional status and physical development, condition of dysphagia, and pneumonia before and after 3-month treatment were compared.

NCT ID: NCT06268223 Recruiting - Cerebral Palsy Clinical Trials

Home-Based Action Observation Training for Chewing and Swallowing Function

Start date: October 13, 2023
Phase: N/A
Study type: Interventional

The goal of this clinical trial is to investigate the effects of home-based Action Observation Training (AOT) applied together with Functional Chewing Training (FuCT) on chewing and swallowing functions and feeding behavior in children with Cerebral Palsy (CP) who have chewing disorders. The main questions it aims to answer are: - Is the application of Home-Based AOT together with FuCT effective on chewing function in children with CP? - Is the application of Home-Based AOT together with FuCT effective on swallowing function in children with CP? - Is the application of Home-Based AOT together with FuCT effective on feeding behavior in children with CP? Within the scope of the study, children with CP will be divided into two groups as the study group and the control group. All groups will implement FuCT routines, comprising 5 sets per day, 5 days a week, for 12 weeks. Additionally, the study group will be included in an AOT program, conducted via telerehabilitation, for 1 set per day, 3 days a week, for 12 weeks, with the guidance of a physiotherapist. All children with CP will be evaluated at the beginning, after 6 weeks, and at the end of the study.

NCT ID: NCT06266286 Recruiting - Cerebral Palsy Clinical Trials

EXOPULSE Mollii Suit & Cerebral Palsy

EXOCEP
Start date: September 13, 2023
Phase: N/A
Study type: Interventional

Spasticity is a frequent and debilitating symptom in patients with cerebral palsy. It can alter the patients' balance, mobility, as well as their quality of life (QoL). The available therapeutic strategies for treating spasticity and related symptoms are usually faced with limited efficacy and numerous side effects. For these reasons, non-invasive stimulation techniques, namely transcutaneous electric nerve stimulation using EXOPULSE Mollii suit, might be of help in this context.

NCT ID: NCT06262191 Active, not recruiting - Cerebral Palsy Clinical Trials

Testing an Adjustable Ankle Orthosis During Walking in Cerebral Palsy

Start date: May 1, 2024
Phase: Early Phase 1
Study type: Interventional

This study seeks to determine how an adjustable stiffness ankle braces affects walking performance and biomechanics in cerebral palsy.

NCT ID: NCT06259864 Recruiting - Cerebral Palsy Clinical Trials

Effects of Mollii Suit in Children With Non-Ambule Cerebral Palsy

Start date: January 20, 2024
Phase: N/A
Study type: Interventional

The aim of our study is to examine the effectiveness of the Mollii Suit application on gross motor function, spasticity, postural control, upper extremity skills, selective motor control, daily living activities, quality of life, pain, sleep, constipation and drooling problems in non-ambulatory individuals with cerebral palsy (CP).

NCT ID: NCT06259643 Recruiting - Cerebral Palsy Clinical Trials

Effects of Power Wheelchair Soccer for Individuals Presenting With Physical Impairments

chair-soccer
Start date: November 1, 2023
Phase: N/A
Study type: Interventional

This study is a prospective interventional study. It will be conducted at a single center with participants who have neuromotor impairments. The primary objective is to assess and measure the clinical and psychosocial effects of a season of power wheelchair soccer among its participants presenting with severe motor impairments due to neuromuscular lesion. A maximum of twenty participants will be recruited and included in the same group. Data collection will be performed before, during, and after the wheelchair soccer season. The study will span the entire season, starting in November 2023 and ending in June 2024. Clinical and psychosocial assessments will be conducted every 3 months. Each assessment session will last 2 hours per participant. Before and after the wheelchair soccer season matches, we will evaluate parameters related to the physical load of the sport. These evaluations will last 10 minutes per participant.

NCT ID: NCT06256887 Enrolling by invitation - Cerebral Palsy Clinical Trials

Sleep Spindles Organization as an Early Neural Marker of Neuromotor Outcome

SONNO
Start date: November 30, 2023
Phase:
Study type: Observational

The goal of this observational study is to test the effectiveness of quantitative early biomarkers in the sleep electroencephalogram (EEG), namely sleep spindles, as predictors of early sensorimotor maturation and long-term motor outcome. Spindles are discrete events, prominent over sensorimotor areas, that reflect motor learning overnight consolidation. They represent a potential marker for the investigation of altered early sensorimotor reorganization and long-term motor outcomes in the case of neuromotor pathologies. To test this hypothesis, we will validate the prognostic accuracy of a semi-automated EEG sleep-spindles analysis in two clinical populations: 1) infants with a perinatal brain lesion, at risk of Cerebral Palsy (CP), 2) infants with Spinal muscular atrophy type 1 (SMA1), a neuromuscular disease detectable at birth with variable response to early pharmacological treatment. A group of typically developing infants (at very low neurological risk) will be enrolled in the study as control group. All participants will undergo two sleep EEG recordings at 2-5 months (T1) and 12 months (T2), respectively. Short-term neuromotor outcome will be evaluated at T1 and T2, through standard and validated assessment. Long-term neuromotor development will be defined at 18 months (T3; i.e. CP vs NO CP; SMA treatment responders vs No responders). Primary clinical and motor outcomes will be used for estimating the effectiveness of spindles' features at T1 and T2 as predictors of later clinical and motor outcomes at T3. EEG sleep features will be considered both cross-sectionally, at each time point (T1, and T2), and from a longitudinal perspective. Differences in the EEG sleep-spindle features will be evaluated within- and between-groups.

NCT ID: NCT06251531 Completed - Cerebral Palsy Clinical Trials

Goal-Directed Therapist-Guided Play-Based Intervention in Children With Cerebral Palsy

Start date: January 18, 2019
Phase: N/A
Study type: Interventional

Abstract Objective: This study planned to examine the effect of Goal-Directed Therapist-Guided Play-Based Intervention (GD-TG-PBI) on occupational performance, occupational satisfaction and functional performance in children with diplegic cerebral palsy (DCP). Materials and Methods: This study was designed as a randomized controlled trial. 34 children with DCP (14 boys; 20 girls) who received routine therapy included to the study. All children were classified according to the Gross Motor Function Classification System (GMFCS) and the Manual Abilities Classification System (MACS). Participants were randomly divided into two groups: the GD-TG-PBI group (number =17; mean age: 7.70±2.25 years) and the control group (number =17; mean age: 7.41±2.06 years). Both groups received routine therapy twice a week for 45 minutes per session during 8 weeks; while the GD-TG-PBI group received GD-TG-PBI additional to routine therapy twice a week for 45 minutes per session during 8 weeks. Occupational performance and satisfaction were determined with the Canadian Occupational Performance Measure (COPM), and functional performance was evaluated with the Pediatric Evaluation of Disability Inventory (PEDI). The COPM and PEDI were performed before and after the intervention for both groups. DÄ°fferences between COPM and PEDI values before and after the intervention calculated, additionally the effect size of each parameter calculated.

NCT ID: NCT06245733 Recruiting - Cerebral Palsy Clinical Trials

Study of the Effect of Compassion-Based Education Program Applied to Mothers of Children Diagnosed With Cerebral Palsy

Start date: September 1, 2023
Phase: N/A
Study type: Interventional

Purpose of the study; The aim of this study is to examine the effect of a compassion-based education program applied to mothers of children with cerebral palsy on compassion fatigue, depression, and psychological resilience.

NCT ID: NCT06244901 Recruiting - Cerebral Palsy Clinical Trials

Community Testing of Wearable Assistance

Start date: October 25, 2023
Phase: Early Phase 1
Study type: Interventional

This feasibility study looks to evaluate ankle exoskeleton assistance in community settings for individuals with cerebral palsy.