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NCT ID: NCT05588089 Completed - Mothers Clinical Trials

The Effect of Baby Care Training Given to Fathers After Birth

Babycare
Start date: February 4, 2022
Phase: N/A
Study type: Interventional

The aim of this study is to provide infant care training to fathers and to measure father-infant attachment and maternal postpartum depression and quality of life.

NCT ID: NCT05587946 Enrolling by invitation - Nurse's Role Clinical Trials

The Effect of Virtual Reality Application Used During Endoscopy on Pain, Anxiety and Vital Signs: A Mixed Methods Study

Start date: January 15, 2022
Phase: N/A
Study type: Interventional

In this study, the effect of virtual reality application used during upper gastrointestinal endoscopy on pain, anxiety and vital signs will be investigated. The research will be conducted as a mixed methods research including quantitative and qualitative methods. The exploratory sequence mixed design model, one of the mixed method designs, will be used in the research.

NCT ID: NCT05587712 Recruiting - Clinical trials for Pulmonary Arterial Hypertension

Study to Evaluate Sotatercept (MK-7962) in Children With Pulmonary Arterial Hypertension (PAH) (MK-7962-008)

MOONBEAM
Start date: January 19, 2023
Phase: Phase 2
Study type: Interventional

The primary objectives of the study are to evaluate the safety and tolerability, and pharmacokinetics (PK) of sotatercept over 24 weeks of treatment in children ≥1 to <18 years of age with PAH World Health Organization (WHO) Group 1 on standard of care (SoC). There is no formal hypothesis.

NCT ID: NCT05587647 Completed - Clinical trials for Intellectual Disability

The Effect of Transition to Adulthood Education Program on Family Quality of Life and Perceived Stress Level

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

Negative emotions experienced during life processes and the burden of caregiving affect the quality of life of parents. It has been found that parents who care for their children with intellectual disability (ID) for a long time have difficulties in coping with stress and their quality of life is adversely affected. However, families play a key role in maintaining the care of their children with ID, so it is very important that parents are supported in the matters they need.

NCT ID: NCT05587101 Recruiting - Multiple Sclerosis Clinical Trials

Neurogenic Lower Urinary Tract Symptoms in Patients With Multiple Sclerosis

Start date: October 19, 2021
Phase:
Study type: Observational [Patient Registry]

There is no consensus in the literature upon the neurourological diagnostic algorithm of the patients with multiple sclerosis (MS). The primary aim of the study is phenotyping the patients with MS. These phenotypes might guide Neurology and Urology specialists during diagnosis and treatment. Secondary aim of this study is to define the presence and severity of urological symptoms' and disorders', involving the patients with diagnosis of MS less than 5 years into a urological follow-up and treatment process. Our study might include 4 visits (the first visit, 3rd month, 6th month and 12th month visit). Questionnaires, uroflowmetry and bladder diary might be repeated on each visit. Filling cystometry and pressure-flow study will be performed only on the first visit. All patients will receive 6 different questionnaires which aim to define the severity and presence of lower urinary tract symptoms. Bladder diary is an online application which will represent at least 3 days of frequency, urgency, incontinence episodes and the amount of fluid intake, and urination. The phenotypes would be defined after performing the first visit diagnostic tools (all of the tools are necessary during the diagnostic algorithm of neurogenic lower urinary tract symptoms). The phenotypes will be defined as: a. no symptoms with normal urodynamics, b. Lower urinary tract symptoms with normal urodynamics, c. no symptoms with abnormal urodynamics, d.lower urinary tract symptoms with abnormal urodynamics. During a follow-up period of 1 year, changes in the bladder diaries and scores in questionnaires of these groups will be compared on each visit.

NCT ID: NCT05586633 Recruiting - Clinical trials for Low Back Pain, Posterior Compartment

The Efficacy of Ultrasound-guided Ozone Injection in the Treatment of Patients With Chronic Low Back Pain

Start date: November 1, 2021
Phase: N/A
Study type: Interventional

Low back pain is a common disorder that every individual in the society is likely to meet throughout his/her life. Low back pain lasting longer than 12 weeks is defined as chronic low back pain and causes serious disability in the community. Conservative, pharmacological, interventional and surgical treatment options are available in its treatment. In this study, it was aimed to determine the effects of ultrasound-guided deep paravertebral periforaminal ozone injection treatment on physical examination, functional independence, quality of life and pain scores in patients with chronic low back and leg pain and to compare it with transforaminal epidural steroid injection treatment.

NCT ID: NCT05586412 Recruiting - Clinical trials for Being in the 18-50 Age Population

Efficacy of Auricular Vagus Nerve Stimulation

Start date: July 7, 2022
Phase: N/A
Study type: Interventional

Auricular Vagus Nerve Stimulation, a non-invasive method, will be used in the study. Studies have shown that vagus nerve stimulation combined with a large vagal nerve network can have a neuromodulatory effect that will activate some natural protective pathways to improve health. Clinically, vagus nerve stimulation is FDA-approved for epilepsy, treatment-resistant depression, and morbid obesity. Since OSS dysfunction is also involved in the etiology of DO and there is no study on the effectiveness of vagus nerve stimulation in this disease, this study is planned to reveal the effectiveness of auricular vagus nerve stimulation and home exercise program in DO patients.

NCT ID: NCT05585853 Not yet recruiting - Pain Clinical Trials

The Effect of Virtual Reality Glasses on Pain Level and Hemo-Dynamic Variables After Open Heart Surgery

Virtual
Start date: January 15, 2024
Phase: N/A
Study type: Interventional

In this study, between 15 November 2022 - 15 November 2023, who met the inclusion and exclusion criteria, a total of 82 patients who are on the 2nd or 3rd day after the surgery and who are hospitalized in the cardiovascular surgery intensive care clinic will be recruited.

NCT ID: NCT05585840 Completed - Pediatric Cancer Clinical Trials

The Effect of Biofeedback-Based Virtual Reality Game on Children

Start date: July 15, 2023
Phase: N/A
Study type: Interventional

The needles of port catheters, which are often used in childhood cancer treatment, must be changed every 5-7 days, which causes pain, anxiety, and fear in children every 5-7 days In recent years, the usage of virtual reality has grown to distract children during port catheter needle insertion. But it's not always easy for children to switch their attention to something else. A good child distractor must be sensory-stimulating, developmentally appropriate, and highly interactive.

NCT ID: NCT05585749 Completed - Anxiety Clinical Trials

Virtual Reality Application on Pain Intensity and Anxiety Level in Endoscopy Patients

Start date: September 5, 2022
Phase: N/A
Study type: Interventional

With the virtual reality application in patients with bronchoscopy, it is aimed to reduce the fear, stress and tension arising from the possibility of the development of pain and complications in the patients. The research will be carried out in the form of pretest-posttest application with 30 experimental and 30 control groups. The researcher aims to minimize the fear and stress in the patient by applying the virtual reality application to the patient in the experimental group 10 minutes before the procedure and 5-10 minutes during the procedure.