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NCT ID: NCT05850351 Recruiting - Virtual Reality Clinical Trials

Virtual Reality Based Tele-Exercises on Exercise Capacity in Cystic Fibrosis

Start date: May 30, 2023
Phase: N/A
Study type: Interventional

The goal of this clinical trial is to investigate the effects of a-12-week virtual reality exercise program, applied as tele-exercise, on the exercise capacity of children with cystic fibrosis, whose physical activity level is further restricted during the pandemic. The main questions it aims to answer are: Does aerobic tele-exercise increase functional capacity in cystic fibrosis patients? Will there be a difference in treatment outcomes between the virtual reality group and the online exercise group? Participants will be randomized into two groups; virtual reality group and online group. Physical activity will be provided to the virtual reality group in the form of team activities in a virtual environment, and the other group will be provided online exercises at their home. For this purpose, virtual reality headsets will be provided to patients to give the impression of a natural, immersive environment and realistic experience. Researchers will compare exercise compliance and functional capacity between the virtual reality group and the online group.

NCT ID: NCT05850338 Completed - Quality of Life Clinical Trials

Determination of the Effects of Autogenic Relaxation Exercise and Cold Pillow Application on Vasomotor Symptom Control and Quality of Life in Postmenopausal Women

Vasomotor
Start date: June 22, 2018
Phase: N/A
Study type: Interventional

The aim of this study was to determine the effect of autogenic relaxation exercise and cold pillows on vasomotor symptom control and quality of life. This randomized controlled study was carried out at Kirikkale University Faculty of Medicine Hospital, Department of Obstetrics and Gynecology, Gynecology Department between 22.06.2018 and 02.01.2019. The sample of the study consisted of 88 people, 44 in the intervention group and 44 in the control group. Since there were case losses in the research, the research was completed with a total of 69 people, 34 in the intervention group and 35 in the control group. The women in the intervention group performed autogenic relaxation exercises and cold pillow application for 8 weeks, and the women in the control group received outpatient care in the hospital. Research data were collected using Descriptive Characteristics Form, Menopause-Specific Quality of Life Scale, Vasomotor Symptom and Practice Follow-up Diary. Data collection tools were applied to the women during the first interview, and at the 4th and 8th weeks after the women were included in the study. In the analysis of descriptive data; number, percentage, mean and standard deviation were used. Independent groups t test was used to determine the difference between groups. The relationship between two independent categorical variables was analyzed using the chi-square test. Variables between dependent groups were compared in repeated measurements with anova test and mixed anova test

NCT ID: NCT05850169 Completed - Executive Function Clinical Trials

The Effects of Creative Dance Therapy on Motor and Executive Functions in Children With Dyslexia

Start date: August 24, 2019
Phase: N/A
Study type: Interventional

Although some benefits of dance have been described for motor and cognitive skills, the effects on individuals with dyslexia are unclear. The purpose of this study was to investigate the effects of creative dance training on the motor and executive skills of children with dyslexia.

NCT ID: NCT05850104 Completed - Clinical trials for Traumatic Amputation

Comparison of Classical Prosthesis and Silicone Prosthesis

Start date: May 24, 2023
Phase:
Study type: Observational

The purpose of this study is to investigate the effects of classical Chopart prosthesis and silicone prosthesis on socket comfort, satisfaction level and quality of life in patients with unilateral Chopart amputation.

NCT ID: NCT05850065 Recruiting - Clinical trials for Gingival Recession, Localized

Assessment of Gingival Health Following Rubber-Dam Isolation

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

The aim of this study is to evaluate the effect of retraction techniques on gingival health. Four different method (212 clamp (Hu-Friedy, USA); Brinker B4 clamp (Coltene Hygenic, USA); dental floss using the simple knot tie method; and using the simple knot tie and 212 clamp together) will evaluated. After rubber dam isolation restorations will be performed, each restoration will take maximum 30 minutes. Changes in periodontal tissues will be evaluate; using plaque index, bleeding on probing, probing depth, keratinized gingiva, attached gingiva, relative gingival margin level, relative attachment level and VAS (visual analogue scale) scoring and patient comfort levels after the procedure at different times (pre-restoration, after restoration, 1 week, 1 month, 3 month). The evaluation time is planned not to exceed 10 minutes, restorations are done by a single specialist in Marmara University Restorative Dentistry Department.

NCT ID: NCT05850052 Recruiting - Surgery Clinical Trials

McGrath Videolaryngoscopy and Direct Laryngoscopy Rapid Sequence Intubation

Start date: May 7, 2023
Phase: N/A
Study type: Interventional

The study seeks to compare the efficacy of conventional direct laryngoscopy using a Macintosh blade with the McGrath videolaryngoscope for rapid sequence endotracheal intubation.

NCT ID: NCT05849571 Completed - Oral Mucositis Clinical Trials

Investigation of the Effect of Oral Care With Coconut Oil on the Degree of Oral Mucositis in Pediatric Oncology Patients

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

Oral mucositis is characterized by ulcerative and inflammatory changes in the oral mucosa and is frequently seen in pediatric oncology patients receiving chemotherapy. Oral mucositis negatively affects the child's daily life functions, nutrition and quality of life. Pain is the most commonly reported side effect in mucositis. Pain impairs patients' ability to chew, swallow and speak, leading to inadequate fluid/nutrient intake, malnutrition and communication problems. Weight loss, dehydration, mucosal ulceration, fluid-electrolyte imbalance may develop in patients who cannot be fed adequately, and total parenteral nutrition (TPN) can be started. Other important complications of oral mucositis are oral bleeding and infection. The ulcerated oral mucosa creates an entrance gate for microorganisms, increasing the risk of bacterial/fungal/viral infections. Infections may be limited only to the oral mucosa, as well as systemic infection and septicemia. As a result, the length of hospital stay of the patients increases, the treatment costs increase and their quality of life deteriorates. Therefore, early diagnosis of oral mucositis, planning and implementation of oral care are important. Responsibility of nurses in the management of oral mucositis; monitoring the oral cavity for symptoms, diagnosing mucositis, providing appropriate oral care, and educating patients. In this context, it is extremely important to prevent oral mucositis, to evaluate the oral mucosa using a scale, and to reduce the degree of oral mucositis, that is, to perform appropriate oral care for its recovery, in terms of preventing other health problems and ensuring the well-being of the child. The aim of this thesis is to determine the effect of oral care with coconut oil on the degree of oral mucositis in pediatric oncology patients.

NCT ID: NCT05848596 Completed - Hand Hygiene Clinical Trials

Handwashing Knowledge and Practice of Palliative Care

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

This study was planned as a randomized controlled study to evaluate the effect of hand hygiene training given to the companions in the palliative care service with standard patient simulation on hand washing knowledge and practices. Companions who are over the age of eighteen, who are at least literate, who can communicate effectively, and who fully fill in the data collection tools will be included in the study. The key questions it aims to answer Does the hand hygiene training given with standard patient simulation have an effect on the hand washing knowledge of the attendants? Do the attendants participating in the hand hygiene training given with standard patient simulation have an effect on hand washing practices?

NCT ID: NCT05848336 Completed - Clinical trials for Autism Spectrum Disorder

The Gluten-Casein-free Diet in Children With Autism: A Clinical Results of the Ophthalmic and Behavioral Manifestations

Start date: November 26, 2020
Phase: N/A
Study type: Interventional

To evaluate the efficacy of eight weeks of GFCF in children with ASD on autistic symptoms and ophthalmic findings such as corneal reflex, interpupillary distance (IPD) and pupil size.

NCT ID: NCT05847946 Completed - Clinical trials for Pregnancy-related Low Back Pain

The Effect of Kinesio Taping on Pain and Disability in Pregnancy-Related Low Back Pain

Start date: June 4, 2023
Phase: N/A
Study type: Interventional

Pregnant women may experience pregnancy-related low back pain and this pain may negatively affect function. There are studies in the literature that Kinesiotape applications improve pain. There is no study examining the effect of Kinesiotape application in addition to exercise on pregnancy-related low back pain and function. At the end of our study, we will compare the effects of Kinesiotape application for a total of 8 sessions for 4 weeks on pain and function.