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NCT ID: NCT05324644 Completed - Clinical trials for Codependency, Psychological

The Effect of Motivational Interview Attempt on Self-Efficacy Level and Decision to Quit Smoking of University Students

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

This study aimed to determine the effect of motivational interview initiatives on the smoking cessation decisions of university students. In this study, which will be conducted as a randomized, case-control study; Student introduction form, Fagerström Nicotine Addiction Test, Decision-Making Balance Scale, Self-efficacy adequacy scale, Behavior Change Stage Diagnosis Short Questionnaire, Beck Depression Scale, Smoking Desire Scale will be used, CO will be measured. Motivational interview initiative will be applied to first-year students who are enrolled in the university, who smoke and are considering quitting. The estimated duration of the study is 8-10 months. Maximum number of volunteers will be 60.

NCT ID: NCT05324527 Completed - Anxiety Clinical Trials

The Effect of Preoperational Hand Massage Anxiety Level And Hemodynamic Variables

Start date: April 1, 2017
Phase: N/A
Study type: Interventional

The study was conducted randomly controlled experimental to determine the effect of hand massage applied to pre-operative children on anxiety level and physical symptoms of anxiety.

NCT ID: NCT05324215 Recruiting - Postoperative Pain Clinical Trials

Transversalis Fascia Plane Block and Rectus Sheath Block in Renal Transplantation Donors

Start date: February 17, 2022
Phase: N/A
Study type: Interventional

Transversalis fascia plane block (TFPB) is a relatively new, easy-to-apply and safe regional anesthesia technique used to provide postoperative analgesia in various surgeries. It has been shown that TFPB and rectus sheath block (RSB) administration reduces opioid consumption and related side effects in patients undergoing surgery with general anesthesia. To our knowledge, there is no study examining TFPB in donor nephrectomy. The investigators aimed to prospectively examine the effect of TFPB and RSB on opioid consumption in postoperative period on donors who will undergo laparoscopic nephrectomy in renal transplantation surgery.

NCT ID: NCT05323942 Completed - Clinical trials for Sleep Bruxism, Childhood

The Effect of Sleep Hygiene and Exercise Therapy in Children With Sleep Bruxism

Start date: March 8, 2020
Phase: N/A
Study type: Interventional

The aims of this study were to determine the relationship between sleep bruxism, oral habits, and sleep habits and establish treatment approaches in children.

NCT ID: NCT05323903 Completed - Clinical trials for Postpartum Hemorrhage

The Effect of Game-Based Learning and Telesimulation on Nursing Students' Management of Postpartum Hemorrhage

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

This study was conducted to evaluate the effects of Kahoot and telesimulation methods on the knowledge, skills, motivation and clinical performance of nursing students in the management of postpartum hemorrhage and to examine the students' views on these methods. This is a randomized controlled intervention study in which the quantitative research method is used. The study sample consisted of year-2 students (n=177) who took the Obstetrics and Gynecology Nursing course in the spring semester of the 2020-2021 academic year at the Faculty of Gulhane Nursing at SBU. The control group consisted of 44 students, and the intervention group was divided into three groups and randomized to include 44 students in each group, with a total of 133 students. All students attended the "Postpartum Hemorrhage and its Management" course, and after the course, Group II received the telesimulation intervention, Group III the Kahoot game intervention and Kahoot game and telesimulation to Group IV. The control group did not receive any intervention.

NCT ID: NCT05323539 Completed - Thyroid Clinical Trials

Comparison of Thyroid Volumes in Patients With and Without Endometrioma

Start date: September 20, 2021
Phase: N/A
Study type: Interventional

The aim of our study is to evaluate whether there is a statistical difference between thyroid gland volume in patients with pathological diagnosis of endometriosis or endometrioma and in patients who underwent surgery for other gynecological reasons, and to reveal the presence of concomitant thyroid disease in these cases.

NCT ID: NCT05323006 Completed - Clavicle Clinical Trials

Scapular Stabilization Exercises on the Clavicular Movement

Start date: June 20, 2017
Phase: N/A
Study type: Interventional

This study was planned to indicate efficiacy of the scapular stabilization exercises on the clavicula movements.

NCT ID: NCT05322915 Completed - Multiple Sclerosis Clinical Trials

Therapeutic Effects of Line Dancing in People With MS

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

The objective of this study is to analyze the effects of line dancing on balance, anxiety, depression and quality of life for people with multiple sclerosis (PwMS).

NCT ID: NCT05322291 Completed - Clinical trials for Chronic Kidney Failure

The Effect of the Mobile Application Developed for Hemodialysis Patients on Symptoms and Disease Compliance

Start date: March 28, 2022
Phase: N/A
Study type: Interventional

The aim of this study is to determine the effect of mobile-based education and counseling developed for hemodialysis patients on the symptoms experienced and the adaptation to the disease.

NCT ID: NCT05321966 Completed - Quality of Life Clinical Trials

The Effect of Video Training on Symptom Burden Patients Undergoing Hemodialysis Treatment

Start date: April 15, 2021
Phase: N/A
Study type: Interventional

Purpose: This study aimed to examine the impacts of video training support on the symptom burden, comfort level and quality of life (QoL) of the patients undergoing hemodialysis (HD) treatment. Methods: The current study adopted a randomized controlled quasi-experimental research design to investigate the implications of video training support on the symptom burden, comfort level and QoL of 48 participant patients, 22 of whom were in control and 26 were in intervention group, at Mugla Fethiye State Hospital Hemodialysis Center and a private hemodialysis center between April 2021 and July 2021. Data collection was conducted through Dialysis Symptom Index (DSI), Patient Information Form, QoL Scale Short Form (SF 36), and Hemodialysis Comfort Scale (HDCS) Version II. The data was collected four times, in week 0 (1st measurement), 4th week (2nd measurement), 8th week (3rd measurement), and 12th week (4th measurement). The intervention group watched three episodes of a training video a week for 12 weeks. Each session started 90 minutes after the HD treatment. The control group was shown the training video at the end of the research. Necessary ethics committee, institutional permissions and written consents of the participant patients were obtained prior to the study.