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NCT ID: NCT06377891 Enrolling by invitation - Depression Clinical Trials

The Effect of Emotional Resilience Training on Fear of Birth and Depression in Primiparous Pregnant Women

Start date: April 16, 2024
Phase: N/A
Study type: Interventional

Although birth has a great place in a woman's life, factors such as the woman's education level, personal experiences, social support status, whether the pregnancy is planned or not, the family's attitude towards pregnancy, and socioeconomic status increase the burden of pregnancy and can create a stressful situation for the woman. While the pain that may be experienced during birth, thoughts about the baby's health and postpartum baby care further increase this fear, primiparous women who will give birth for the first time experience many emotions that they cannot define and cannot predict the situations they will encounter during birth. The most important situation that will cause pain during birth is fear. So much so that fear of birth may cause women to avoid pregnancy and increase optional abortions.In particular, fear of birth may increase cesarean delivery rates and also lead to negative maternal outcomes such as poor mental health after birth. Fear experienced during the antenatal period can lead to difficult births, mother-baby attachment problems, and depression. While fear of birth causes depression and anxiety disorders in the postpartum period, it is stated that depression experienced during pregnancy may increase the fear of birth, or fear of birth may be a hidden symptom of depression. It is noted that emotional regulation skills and resilience in pregnant women can be effective strategies in minimizing and managing fear, anxiety, stress, and anxiety. Emotional resilience is defined as the style of coping with stress, the ability to repair oneself, the ability to recover from adverse events quickly, and the state of adapting to a new environment. In particular, individuals with high emotional resilience can protect their physical and mental health and increase their life satisfaction by reducing the negative consequences they experience. With the emotional resilience training given during pregnancy, pregnant women's stress, fear, and anxiety will be reduced, and they will be able to cope better with the difficulties they experience. This research will be conducted to examine the effect of emotional resilience training given to primiparous pregnant women on fear of childbirth and depression.

NCT ID: NCT06376370 Enrolling by invitation - Quality of Life Clinical Trials

The Effect of a Computer-Assisted Rehabilitation Program on Epilepsy Patient

Start date: April 26, 2024
Phase: N/A
Study type: Interventional

The aim of this study is to examine the effects of the RehaCom Computer-Assisted Rehabilitation Program Applied to Epilepsy Patients on Self-Management, Cognitive Function and Quality of Life.

NCT ID: NCT06376357 Enrolling by invitation - Breast Neoplasms Clinical Trials

The Effect of Foot Massage With Roles on Cancer Patients

Start date: April 27, 2024
Phase: N/A
Study type: Interventional

It was aimed to examine the roles in the management of treatment-related peripheral neuropathy in cancer patients receiving taxane-based chemotherapy and the effect of foot massage on neuropathy and quality of life.

NCT ID: NCT06376344 Enrolling by invitation - Cancer Clinical Trials

The Effect of Tennis Ball on Balance and Quality of Life in Cancer Patients With Neuropathy.

Start date: April 28, 2024
Phase: N/A
Study type: Interventional

This research; It was aimed to evaluate the effect of myofascial release using a tennis ball on balance and quality of life in cancer patients who developed peripheral neuropathy.

NCT ID: NCT06374940 Enrolling by invitation - Gynecologic Disease Clinical Trials

Surgical Outcomes of Conventional Hysterectomy or Manipulator-assisted Abdominal Hysterectomy

Start date: April 17, 2024
Phase: N/A
Study type: Interventional

Objective: The comparison of surgical outcomes conventional hysterectomy and manipulator-assisted hysterectomy Study design: Prospective randomized controlled trial. Allocation to either group occurred via computer-generated random numbers. Sequentially numbered, opaque envelopes were prepared according to randomization. The patients were unaware of whether they would undergo a conventional hysterectomy or manipulator-assisted abdominal hysterectomy for their surgical procedure. The research coordinator unveiled group assignments upon individual patient recruitment by opening the corresponding envelope. Study population: Inclusion criteria were patients aged 40-70 years who underwent hysterectomy for benign gynecological indications. Primary outcomes: (1) Operation Time. Secondary outcomes: (1) Postoperative early pain (Visual Analog Score (VAS) at 6th and 24th hours of the surgery) (2) intraoperative complications, (3) postoperative complications

NCT ID: NCT06374004 Enrolling by invitation - Clinical trials for Subacromial Pain Syndrome

The Effect of Thoracic Mobilization in Individuals With Subacromial Pain Syndrome

Start date: April 10, 2024
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate the effect of six-week thoracic mobilization on pain intensity, muscle tone, functional and muscle activation in individuals with subacromial pain syndrome.

NCT ID: NCT06369844 Enrolling by invitation - Clinical trials for Pressure Injury Prevention

Pressure Injury Education Intervention for Pediatric Intensive Care Nurses: A Randomized Controlled Trial

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

The purpose of this observational study is to find out the impact of pressure injury education on the knowledge level of pediatric intensive care nurses and the likelihood of pediatric pressure injury occurrence. The main questions it aims to answer are: - Does pressure injury education increase nurses knowledge level on pediatric pressure injuries? - Does the rate of pediatric pressure injuries decrease after the education? The researcher will compare nurses working in two separate pediatric intensive care units where similar patients are treated to see if planned education on pressure injuries affects nurses knowledge level and the rate of pediatric pressure injuries. - Volunteer nurses participating in the study will answer pressure injury survey questions prepared by the researcher. - Nurses in the intervention group will attend planned education sessions provided by the researcher. - Two weeks after the completion of the education sessions, all nurses in the intervention and control groups who wish to continue participating in the study will answer the pressure injury survey questions prepared by the researcher again.

NCT ID: NCT06368011 Enrolling by invitation - Stigmatization Clinical Trials

The Impact of Acceptance and Commitment Therapy on Stigmatization

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

The goal of study is to determine the effect of acceptance and commitment therapy-based psychoeducation on the level of stigmatization applied to relatives of schizophrenia patients. Type of study: This study was planned as a pretest-posttest quasi-experimental design with an observation and control group. Participants: The population of the study consisted of the relatives of schizophrenia patients who were registered and actively attending the Community Mental Health Center in a state hospital in Ankara. Intervention: Before the psychoeducation process started, personal information form and scales were applied to the relatives of the patients in the experimental and control groups. An ACT-based psychoeducation program consisting of 8 sessions was applied to the experimental group. each session lasted approximately 90 minutes. The control group did not receive any intervention. After the psychoeducation, the scales were reapplied to the experimental and control groups. In addition, the experimental group was asked to fill out the psychoeducation evaluation form. The scales were reapplied to the experimental group after the 1-month follow-up study and evaluated.

NCT ID: NCT06360146 Enrolling by invitation - Cardiac Disease Clinical Trials

Early Mobilisation of Post Cardiac Surgery in Geriatrics.

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

Heart and blood vessel problems together referred to as cardiovascular diseases (CVD) include congenital heart disease, cerebrovascular illness, and coronary heart disease. Following heart surgery, patients who are active in the postoperative phase stay in the hospital for shorter periods of time and experience fewer complications. After cardiac surgery, older adults who exercise during the recovery period experience fewer difficulties and hospitalizations. A total of 100 elderly patients-69 men and 31 women-who had undergone cardiac surgery and were up to 65 years old-voluntarily took part in the study. There were fifty patients in each of the two groups that the participants were divided into: the early mobilization group (Group A) and the control group (Group B). Older patients undergoing cardiac surgery also experienced improved balance as a result of early mobilization and functional exercises.

NCT ID: NCT06348342 Enrolling by invitation - Menopause Clinical Trials

Pelvic Floor Muscle Exercises and Core Exercises in Menopausal Women

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

The prospective and four-arm randomized controlled study was conducted on n = 136 (34 = control, 34 = kegel, 34 = core, 34 = kegel+ core group) menopausal women at Trakya University Health Research and Application Center Urology Polyclinic between Oct 2023 and June 2024. In the first interview, the researcher will apply an information form to all four groups, asking about personal information, habits, bladder irritants and fluid intake-related features, obstetric, gynecological and systemic disease-related features, and stress urinary incontinence-related features. This form will only be filled at the beginning. In addition, the "Pelvic Floor Distress Scale (PFDI)" and "Pelvic Floor Impact Questionnaire (PFIQ)" will be applied and will be repeated by the executive researcher at the 1st, 2nd and 3rd controls. It will be terminated at the 3rd follow-up. Descriptive statistics, Pearson, Spearman's correlation, and regression analyzes will be used in the analysis of research data.