Clinical Trials Logo

Filter by:
NCT ID: NCT05369936 Completed - Dental Anxiety Clinical Trials

Pain Perception: on Relationships Between Dental Anxiety and Olfaction

Start date: March 12, 2018
Phase: N/A
Study type: Interventional

the objective of this study is to evaluate the ability of olfaction in obtaining positive emotional and behavioral responses toward dental anxiety and pain in patients undergoing different dental procedures.

NCT ID: NCT05357937 Completed - Obesity Clinical Trials

Structured Physiotherapy Program in Obese and Non-obese Patients

Start date: December 16, 2020
Phase: N/A
Study type: Interventional

A routine physiotherapy program has been shown to be effective in the prevention and treatment of cardiopulmonary diseases. It also significantly increases functional capacity following coronary artery bypass grafting. However, the effect of a structured physiotherapy program in obese and non-obese patients has not been well explored. As such, the objective of this study is to determine the effect of a standardized physiotherapy program on pulmonary function and walking capacity in obese and non-obese patients undergoing coronary artery bypass grafting. A prospective study was conducted on 50 obese and non-obese individuals who were schedule for coronary artery bypass grafting. Their body mass index was used to separate them into two groups. Both groups followed a structured physiotherapy program from day 1 to day 7 post cardiac surgery. Both groups underwent spirometry and a six-minute walk test at baseline (preoperatively) and after day 4 and day 7 postoperatively. The effect of physiotherapy program on pulmonary function and 6-MWT was assessed using an independent t-test. To estimate the percentage increase or decrease of pulmonary function and distance during 6-MWT for obese and non-obese groups, the percent difference between baseline and posttest data was calculated and compared using an independent t-test. When the normality test failed, the Mann Whitney U test and analysis of variance on rank were used. Chi-square test was used for gender distribution. The results were considered statistically significant if p ≤ 0.05.

NCT ID: NCT05352607 Completed - Cerebral Palsy Clinical Trials

Effect of Transcutaneous Electrical Nerve Stimulation (TENS) on Spasticity in Adult Patients With Spastic Cerebral Palsy

Start date: February 1, 2022
Phase: N/A
Study type: Interventional

Background: Cerebral palsy (CP) is a neurodevelopmental disorder caused by damage of the developing brain and marked by impairments such as increased muscle tone. Physical therapy (PT) is an important element for spasticity management include some modalities as transcutaneous electrical nerve stimulation (TENS). Purpose: To determine the effect of TENS on inhibition of upper limb spasticity in adult patients with spastic cerebral palsy. Methods: Twenty-four adult spastic CP patients aged from 18 to 45 years old with grade 2 to 3 spasticity according to Modified Ashworth Scale will be randomly assigned into two equal groups: TENS group and conventional therapy group. Both groups will receive conventional therapy, while TENS group in addition will receive TENS over elbow flexors with parameter setup of (pulse frequency= 100 Hz, pulse duration= 250 μs, time=30 mints) 3 sessions per week for successive 4 weeks. Outcome measures: Modified Ashworth scale for the spasticity and digital goniometer for elbow joint range of motion, Barthel index scale for upper limb activity of daily living. Follow-up measures will be calculated three times (preintervention, post 2 weeks, and post 4 weeks).

NCT ID: NCT05350241 Completed - Cerebral Palsy Clinical Trials

Repetitive Split-Belt Treadmill Perturbation in Children With Unilateral Cerebral Palsy

Start date: January 3, 2021
Phase: N/A
Study type: Interventional

This study was designed to investigate the effect of repeated split-belt treadmill waking practice on gait symmetry, dynamic balance control, and locomotor capacity in adolescents with unilateral cerebral palsy (ULCP). Fifty-two children with ULCP were randomly allocated to the split-belt treadmill walking (n = 26; undergone split-elt treadmill training or the Control group (n =23, received standard rehabilitation program). Both groups were assessed for gait symmetry, dynamic balance control, and locomotor capacity pre and post-treatment.

NCT ID: NCT05342818 Completed - Clinical trials for Delayed Gastric Emptying

Evaluating Neostigmine Effect on Reducing Gastric Residual Volume as Compared With Metoclopramide and Ondansetron

Start date: April 15, 2022
Phase: Phase 2
Study type: Interventional

One big problem in mechanically ventilated ICU patients is delayed gastric emptying. Delayed gastric emptying in these patients, causes intolerance and high gastric residual volume (GRV) that can lead to abdominal distention, vomiting, increased aspiration risk and consequently increased the length of hospital stay. In this study, investigators will evaluate Neostigmine's effect in reducing GRV in mechanically ventilated patients and compare its effect with metoclopramide and Ondansetron .

NCT ID: NCT05337176 Completed - Clinical trials for Effect of Sleeve Gastrostomy in Both Cognition and Balance

Impact of Sleeve Gastrectomy on Balance and Cognitive Function

Start date: December 1, 2021
Phase:
Study type: Observational

Purpose of the study: Purpose of study is to determine the effect of sleeve gastrectomy on balance and cognitive function in Saudi Arabia. Aim of study: To investigate if there is any change of balance and cognitive function disturbance after sleeve gastrectomy on participant. Research hypothesis: Sleeve gastrectomy have no impact on balance and cognitive function. Inclusion criteria: The participant will be selected according to the following criteria: 1.History of sleeve gastrectomy within 1 to 5 years. 2. Their age between (20-60 years). 3.Ability to walk without any assistive device. 4.All participant should be able to understand all requested instructions Exclusion criteria: The participant will be excluded if they have: 1. Any cognitive disturbances. 2. Disease that may affect balance (Spinal stenosis, peripheral polyneuropathy, vestibular impairment). 3. Gastrectomy operation less than 1year. 4. Pregnancy. Material: 1. Introduction survey (willingness of participant) to recruit sittable participant. 2. Assessment form survey to collected data and result (include MOCA and App-coo application)

NCT ID: NCT05336006 Completed - COVID-19 Clinical Trials

Exercise and Diet for Pediatric Obesity

Start date: March 10, 2020
Phase: N/A
Study type: Interventional

The coronavirus disease (COVID-19), is a communicable pandemic disease as stated by the world health organization (WHO), which has been affecting the world since December 2019. COVID-19 infected children develop the signs and symptoms of the disease, which can be exaggerated or life-threatening when associated with comorbidities like; obesity, sickle cell anemia, immune disorders, chromosomal abnormalities, chronic respiratory or cardiac problems, and congenital malformations.3 It is observed that children affected with COVID-19 who are physically inactive or in a sedentary lifestyle may induce and develop obesity. It is a major health concern in this pandemic situation, which can be addressed and treated with the use of appropriate physical training and proper dietary habits.

NCT ID: NCT05304832 Completed - Clinical trials for Juvenile Idiopathic Arthritis

The Role of Aquatic-Based Plyometric Exercises for Patients With Juvenile Idiopathic Arthritis

Start date: December 6, 2020
Phase: N/A
Study type: Interventional

This study was designed to assess the effect of a 12-week aqua-plyometric (AquaPlyo) training on muscle strength, bone health, and physical ability in children with juvenile idiopathic arthritis (JIA). Forty-eight patients with JIA were randomly allocated to the AquaPlyo group (n = 24, received an aquatic-based plyometric training program, twice/week, over 12 weeks) or the control group (n = 24, received standard exercise program). Both groups were assessed for muscle strength, bone health, and physical ability pre and post-treatment.

NCT ID: NCT05302102 Completed - Cerebral Palsy Clinical Trials

Unilateral Versus Bilateral Lower-Limb Plyometric Training in Children With Cerebral Palsy

Start date: January 6, 2019
Phase: N/A
Study type: Interventional

This study was set out to compare the effect of paretic-limb-only plyometric training versus double-limb training on balance capability and gait symmetry in adolescents with unilateral cerebral palsy (U-CP). Sixty-nine children with U-CP were randomly allocated to the paretic-limb-only plyometric training group (n = 23; performed plyometric movements/exercises unilaterally using the paretic leg only), the double-limb plyometric training group (n = 23; performed plyometric movements/exercises bilaterally through both lower legs), or the Control group (n =23, received standard rehabilitation plus SSC exercises). All groups were assessed for gait-symmetry and balance capability pre and post-treatment.

NCT ID: NCT05301738 Completed - Cerebral Palsy Clinical Trials

Plyometric Exercise-induced Mechano-morphological Changes of Plantar Flexor Muscle-tendon Unit in Cerebral Palsy

Start date: November 1, 2020
Phase: N/A
Study type: Interventional

This study was designed to investigate the effect of three months of plyometric exercise training on the mechanical and morphological properties of the plantar flexor muscle-tendon unit in children with unilateral cerebral palsy (UCP). Thirty-eight children with UCP were randomly allocated to the plyometric exercise group (n = 19, underwent a plyometric training program) or the Control group (n =19, received usual physical rehabilitation alone). Both groups were assessed for the plantar flexors' morphological and mechanical properties before and after treatment.