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NCT ID: NCT06318520 Not yet recruiting - Clinical trials for Dental Enamel Hypomineralization

Clinical Success of Stainless Steel Crowns Applied Using Different Cements

Start date: April 1, 2024
Phase: N/A
Study type: Interventional

The main question of the study was to evaluate the one-year clinical success of SSc bonded with two different cement types in MIH teeth with excessive material loss. The researchears will compare the survival rate, effect on gingival health and radiographic success of calcium silicate-based resin-containing cement and resin-modified glass ionomer cement.

NCT ID: NCT06318455 Recruiting - Clinical trials for Women Receiving Chemotherapy

The Effect of Breathing Exercise on Sleep and Stress Levels in Women With Breast Cancer Receiving Chemotherapy Treatment

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

Women receiving chemotherapy have poor sleep quality and high stress levels. With a method such as breathing exercise, which can be applied at any time without side effects, positive improvements in women's sleep and stress levels can be recorded.

NCT ID: NCT06318429 Not yet recruiting - Clinical trials for Individuals With Diabetes

Evaluation of the Effect of Stretching Exercises Applied to Diabetes Patients on Physiological Parameters and Compliance to Treatment: A Randomized Controlled Study

Start date: March 30, 2024
Phase: N/A
Study type: Interventional

This research will be carried out as a pretest-posttest randomized controlled study to determine the effect of stretching exercises performed 2 days a week for 12 weeks for one hour each session on physiological parameters and treatment compliance in individuals with diabetes.

NCT ID: NCT06318221 Completed - Clinical trials for Head and Neck Cancer

Effects of Perioperative Immunonutrition in Patients With Head and Neck Cancer

Start date: May 1, 2019
Phase: N/A
Study type: Interventional

A prospective randomized controlled study compared the effects of perioperative immunonutrition and standard enteral nutrition (EN) on postoperative short-term outcomes of patients with head and neck (HNC). Five days before surgery and the postoperative day 10, immunonutrition support was given to the intervention group (n=17), and standard EN support was given to the control group (n=17). Body analyses were made, food consumption records were taken, NRS-2002 and quality of life scales were applied, and biochemical parameters were recorded.

NCT ID: NCT06318182 Active, not recruiting - Testicular Cancer Clinical Trials

Testicular Self-Examination Awareness in Young Men

Start date: December 9, 2022
Phase: N/A
Study type: Interventional

This study aims to determine the effect of education based on the health belief model on testicular self-examination awareness and health beliefs in young men. H0 Hypothesis: Education based on the health belief model has no effect on the awareness of testicular self-examination and health beliefs about testicular self-examination of young men in the experimental and control groups. H1a Hypothesis: The training based on the health belief model will increase the awareness of young men in the experimental group about testicular self-examination compared to those in the control group. H1b Hypothesis: The training based on the health belief model will increase the mean scores of the sensitivity subscale of young men in the experimental group compared to those in the control group. H1c Hypothesis: The training based on the health belief model will increase the mean scores of the benefit subscale of young men in the experimental group compared to those in the control group. H1d Hypothesis: The training based on the health belief model will increase the mean scores of the seriousness subscale of young men in the experimental group compared to those in the control group. H1e Hypothesis: The training based on the health belief model will decrease the mean scores of the barriers subscale of young men in the experimental group compared to those in the control group. H1f Hypothesis: The training based on the health belief model will increase the mean scores of the health motivation subscale of young men in the experimental group compared to those in the control group. H1g Hypothesis: The training based on the health belief model will increase the mean scores of the self-efficacy subscale of young men in the experimental group compared to those in the control group.

NCT ID: NCT06318013 Completed - Clinical trials for Impacted Third Molar Tooth

Perineural and Systemic Dexamethasone Use in Dental Surgeries in Terms of Anesthesia Duration and Postop Complaints

Start date: March 27, 2024
Phase:
Study type: Observational [Patient Registry]

Participants will be asked to use some medications after the tooth extraction procedure. These drugs can be used in different ways. Investigators plan to monitor the pain, swelling and duration of anesthesia in the body as a result of participants use.

NCT ID: NCT06317974 Completed - Clinical trials for Breastfeeding Education

The Effect of Breastfeeding Education on Breast Milk Perception and Self-Efficacy in the Pregnancy Health Belief Model

Start date: June 30, 2022
Phase: N/A
Study type: Interventional

Objective: The aim of this study was to evaluate the effect of breastfeeding education based on the Health Belief Model during the antenatal period on couples' perception and self-efficacy regarding breast milk.

NCT ID: NCT06317935 Not yet recruiting - Clinical trials for Hemiplegic Cerebral Palsy

The Effect of Virtual Reality Application on Independence and Hand Functions in Daily Life in Children With CP

Start date: April 23, 2024
Phase: N/A
Study type: Interventional

The aim of this study is to evaluate the effect of virtual reality applications on the level of independence and upper extremity functionality perceived by children in daily life in children with hemipegic cerebral palsy. The research is a randomized controlled, cross-over study. The sample group of the research is children diagnosed with hemiplegic cerebral palsy and families who are receiving inpatient treatment in the pediatric service of Ankara City Hospital Physical Therapy and Rehabilitation Hospital. Two groups, intervention (A) and control (B), will be created from the target research group using the randomization method. The upper extremity functionality of both research groups before the intervention will be evaluated with the 'Motor Activity Diary for Children' scale and the perceived independence level with the 'Children's Hand Use Experience' scale. After the initial evaluation is completed, group A, represented as the intervention group, will receive ArmeoSenso virtual reality intervention in the upper extremity hand function laboratory for 3 weeks, 5 days a week, each session for 30 minutes, in addition to traditional occupational therapy and physiotherapy rehabilitation programs. Meanwhile, group B, represented as the control group, will continue the traditional occupational therapy and physiotherapy rehabilitation program. At the end of the third week of the intervention, tests measuring upper extremity functionality and perceived independence level will be repeated. Measurement tools will be repeated at the beginning of the intervention, at the end of the 3rd week, and at the end of the intervention.

NCT ID: NCT06317571 Completed - Infertility Clinical Trials

Evaluation of The Effect of Fertility Support Education Given to Infertile Couples

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

The aim of the this study was to evaluate the effect of fertility support education given to infertile couples before treatment.

NCT ID: NCT06317116 Enrolling by invitation - Clinical trials for Lower Urinary Tract Symptoms

Examining the Relationship Between Core Muscles and Bladder Issues in Children

Start date: September 29, 2023
Phase:
Study type: Observational

The goal of this observational study is to learn about functional bladder problems in children. The main questions it aims to answer are: - Does bladder symptoms in children have an effect on core muscles? - How do core muscles change based on an increase or decrease in these symptoms?