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NCT ID: NCT05908630 Completed - Clinical trials for Out-Of-Hospital Cardiac Arrest

Accidental Hypothermia in Drowning-related OHCA

Start date: October 1, 2023
Phase:
Study type: Observational

This study aims to report mortality and neurological outcome 180 days after drowning incident in patients with accidental hypothermia vs normothermia following drowning-related OHCA in Denmark during a six-year period from 2016-2021.

NCT ID: NCT05907707 Completed - Aging Clinical Trials

Effects of Gamma-tACS on Memory and Sleep

Start date: June 28, 2023
Phase: N/A
Study type: Interventional

The purpose of this clinical trial is to investigate the feasibility and efficacy of non-invasive transcranial alternating current stimulation (tACS) at gamma frequency in enhancing memory recall and modulating sleep network dynamics measured by at-home electroencephalography (EEG) in healthy elderly people. Eligible participants will first collect sleep EEG at home for one night to acclimate to the data collection during sleep. Participants are then randomized into first undergoing either tACS at gamma band frequencies (i.e. 40Hz) or tACS at a control frequency (i.e. 21Hz). Stimulation is administered in the lab during a cognitive testing battery that includes memorizing items. After a night of sleep with EEG at home, participants return to the lab the following day to measure memory recall. Recall is performed again after five days. This sequence of encoding during stimulation in the lab, sleep EEG at home for one night, and recall is then repeated for the other stimulation condition about a week later. Participants are wearing an actigraphy wristband throughout the study period.

NCT ID: NCT05906940 Completed - Clinical trials for Autonomic Nervous System Imbalance

Vagus Nerve Stimulation for Autonomic Nervous System Activity

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

There are no generally accepted values for transcutaneous vagus nerve stimulation (taVSS application parameters (amplitude, frequency, intensity, duration, side) yet, therefore there are heterogeneous applications in studies. Although positive effects have been shown in different neurological, psychiatric and musculoskeletal diseases, taVSS treatment is not available yet. It is not clear which parameters are important in patient selection.In this study, it was aimed to investigate the change of taVSS effect in healthy individuals according to the level of autonomic nervous system activity before stimulation.

NCT ID: NCT05905757 Completed - Clinical trials for Transversus Abdominis Plane Block

Adjuvant Dexmedetomidine and Tramadol in Subcostal Transversus Abdominis Plan Block

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

In this study, dexmedetomidine and tramadol were added as adjuvant to bupivacaine in transversus abdominis plane block (TAP), intraoperative hemodynamics, opioid consumption, muscle relaxant use, postoperative analgesic effects and side effects (such as nausea-vomiting) were evaluated.

NCT ID: NCT05905094 Completed - Clinical trials for Musculoskeletal Disorder of the Neck

Postural Correction Exercises Effect on Forward Head Posture

Start date: June 10, 2023
Phase: N/A
Study type: Interventional

To determine the effect of postural correction exercise in universities students regarding cervical sagittal posture, head flexion angle in forward head posture.

NCT ID: NCT05902338 Completed - Clinical trials for Attention Deficit Hyperactivity Disorder

Effects of Music on Motor Skills of Children With Attention Deficit and Hyperactivity Disorder

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

Physiotherapists have positive effects on motor skills, executive functions and symptoms of children with attention deficit and hyperactivity disorder. However, progression takes time due to the symptoms of the disease. Physiotherapists need strategies to manage the symptoms of ADHD. Music can be used as a strategy because music is known to reduce the symptoms of children in this group. There is no study in the literature on how motor skills will be affected with musical accompaniment. The aim of this study is to compare motor skills performed with and without music in children with ADHD. When we evaluate motor skills like in a treatment session, the usability of music as an environmental factor will be investigated according to the positive, negative or ineffective results of the music effect.

NCT ID: NCT05902052 Completed - Pain, Postoperative Clinical Trials

Development of Open Heart Surgery Patient Care Protocol and Its Effect on Post-sternotomy Pain

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

Open heart surgery method is generally used in the treatment of cardiovascular diseases. Sternotomy is the process of opening the sternum. After sternotomy, individuals experience ongoing pain in the anterior thorax. Despite developing pain methods and treatments, individuals undergoing cardiovascular surgery suffer from pain that cannot be managed well. Patients undergoing cardiac surgery experience severe pain for the first 48 hours and are in intensive care during this period. Pain is the most important stress factor for intensive care patients. The nurse and health care team should play a key role and take an active role in the management and evaluation of pain. However, there are not enough studies trying to define the role of the nurse in the management of postoperative pain. Protocols are used to provide pain management and routine pain assessment in intensive care units. The use of protocols provides maximum care to the patient, while reducing the cost. It also ensures the patient's participation in the treatment. While protocols ensure that practices are converted into evidence-based ones, they also prevent disruptions in treatment. As a result, management of the pain experiences of patients with sternotomy who underwent open heart surgery in the intensive care unit with the developed protocol; It will guide the improvement and development of pain management. It is thought that the protocol will address the pain of individuals undergoing open heart surgery in a holistic way. In addition, no study has been found in the literature that includes the development of a protocol for the pain of intensive care patients undergoing open heart surgery. For this reason, it is thought that the study will shed light on the literature by being a resource in the management and improvement of pain.

NCT ID: NCT05901701 Completed - Clinical trials for Temporomandibular Joint Dysfunction Syndrome

Efficacy of Low Level LASER Therapy in Treating Temporomandibular Muscle Disorders

RCT
Start date: November 20, 2022
Phase: N/A
Study type: Interventional

This study aimed to evaluate the sustainability of the efficacy of using low level laser therapy and CAD/CAM Michigan splint in improving the range of mandibular movements, muscle activity and reducing the pain.

NCT ID: NCT05901623 Completed - Clinical trials for Neurodevelopmental Abnormality

ASQ Scores of Transient Hypothyroxinemia of Prematurity

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

• Transient hypothyroxinemia of prematurity (THoP) is defined as free thyroxine (FT4) level is below the reference values despite normal TSH level in preterm infant. This study aims to evaluate the neurological development of infants with transient premature hypothyroxinemia (THoP).

NCT ID: NCT05900154 Completed - Clinical trials for RESPIRATORY SYNCYTIAL VIRUS (RSV)

A Study to Learn About the Safety and Immune Activity of RSVpreF in Children 2 to <18 Years of Age

PICASSO
Start date: June 22, 2023
Phase: Phase 1
Study type: Interventional

The purpose of this study is to learn about the safety and immune activity of the vaccine (called RSVpreF) in children 2 to <18 years of age. This study will identify the dose level to be used in Phase 2/3 trials in this age cohort. All participants will receive one injection of RSVpreF. This study has four study visits, two in-clinic and two telehealth visits. Blood samples will be collected for testing. This study is about 6 months long for each participant and will be conducted in the United States.