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NCT ID: NCT06442059 Recruiting - COPD Clinical Trials

Clinical Variables and Dyspnea and Fear of Movement in Chronic Obstructive Pulmonary Patients

Start date: October 1, 2023
Phase:
Study type: Observational

Patients diagnosed with COPD who applied to the Pulmonary Diseases Department of Kırıkkale Yüksek İhtisas Hospital will be included in the study. The aim of our study: It is aimed to investigate the effect of fear of movement due to dyspnea on respiratory function, muscle strength, physical performance and balance in Chronic Obstructive Pulmonary Disease Patients.

NCT ID: NCT06441838 Completed - Clinical trials for Hemodialysis Patients

The Effect of Listening to Surah Inshirah on Mental Health in Hemodialysis Patients.

Start date: February 20, 2024
Phase: N/A
Study type: Interventional

In addition to physical symptoms, mental, social and economic problems may also occur in patients receiving hemodialysis treatment. The most prominent among these problems are psychological problems. It is known that depression and anxiety levels are high in hemodialysis patients.Non-pharmacological methods reduce the patient's pain and anxiety by creating a feeling of comfort and control in the patient. Relaxation techniques such as hypnosis, yoga and music are among these. The main purpose of these methods is to draw the attention of the individual in another direction. Praying is also one of the non-drug methods, and the number of studies on this subject is very limited, and there are studies where it has been determined that praying and praying reduces the anxiety levels of patients.Purpose: To examine the effect of listening to Surah Inshirah on depression, anxiety, stress and mental well-being of hemodialysis patients during treatment. Method: The population of the research will consist of hemodialysis patients who are treated at Mardin Training and Research Hospital, meet the inclusion criteria and volunteer to participate in the research. The study group of 60 people who will participate in the research will be divided into two equal groups according to the table of random numbers obtained from the computer-based Research Randomizer program. Experimental group patients; A patient descriptive characteristics form will be applied, and the pre-test depression, anxiety, stress and mental well-being scale will be applied. Then, Surah Inshirah will be listened to and the final test, the depression, anxiety, stress and mental well-being scale, will be applied. Control group patients; A patient descriptive characteristics form will be applied, and the depression, anxiety, stress and mental well-being scale will be applied. The final test will be applied to the depression, anxiety, stress and mental well-being scale without any intervention.

NCT ID: NCT06440928 Recruiting - Clinical trials for Epicondylitis of the Elbow

Results of Cervical Segmental Mobilization in Patients With Chronic Lateral Epicondylitis

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

The aim of our study was to investigate the effect of cervical segmental mobilization on pain, functionality, grip strength and quality of life in patients with chronic lateral epicondylitis. It was planned as a randomized controlled experimental study.

NCT ID: NCT06440863 Completed - Obesity Clinical Trials

Postoperative BMI Changes and Functional Outcomes in Knee and Hip Arthroplasty

Start date: January 1, 2018
Phase: N/A
Study type: Interventional

PURPOSE Obesity poses challenges to preoperative mobility and functional recovery for arthroplasty patients, yet postoperative weight loss remains elusive. This study aims to investigate postoperative weight changes and their impact on functional scores following knee and hip arthroplasty, exploring factors influencing these changes. METHODS A total of 459 knee and hip arthroplasty cases with a 2-year follow-up were analyzed. BMI and Oxford scores were tracked, alongside factors including comorbidities, corticosteroid use, physiotherapy, and unilateral vs. bilateral surgery. EXPECTED OUTCOMES Based on the study's design and the data available, we anticipate observing the impact of changes in patients' BMI on clinical scores as an independent variable. Additionally, we aim to elucidate the effects of comorbidities, corticosteroid use, physiatrist follow-up, and the type of surgical procedure on both BMI and clinical outcomes. Through this analysis, we expect to gain a comprehensive understanding of how these factors interplay to influence postoperative recovery and overall patient health.

NCT ID: NCT06440356 Completed - Clinical trials for Trigeminal Neuralgia

Effect of Non-invasive Photobiomodulation Therapies in Patients With Trigeminal Neuralgia

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

The aim of this study was to compare the effectiveness of two different photobiomodulation (PBM) therapies as an alternative to medical treatment to reduce pain and improve quality of life in patients with trigeminal neuralgia (TN).

NCT ID: NCT06440096 Completed - Modic Changes Clinical Trials

Complete Blood Count-derived Indexes in Inflammatory Modic Changes

Start date: March 30, 2023
Phase:
Study type: Observational

Some indicators generated from hemogram such as neutrophil/lymphocyte (NLR) have been suggested as biomarkers of systemic inflammation. Type I Modic changes (MCs) have inflammatory nature histologically and are more painful clinically than type II MCs. Therefore, we hypothesized that patients with type I MCs may have increased inflammatory biomarkers and low back pain than those with type II MCs. The aim of this study was to test this hypothesis.

NCT ID: NCT06439680 Completed - Health Behavior Clinical Trials

HASCV-R" Health Programme: a RCT

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

The goal of this randomized controlled trial: is to determine the effect of " HASCV-R " health programme on the health promoting and protective behaviours of the women. The main question it aims to answer are: • Does the HASCV-R program, positively affect the health promoting and protective behaviours of women? The health program was given to the women in the experimental group in five sessions of 40 minutes each for five weeks. The program was implemented to 45 women. After obtaining consent from women, Data were gathered with all participants at the available time and places. The data were collected from the control and experimental groups at two different times, prior to the program was implemented and 3 months after the program was implemented.

NCT ID: NCT06439498 Active, not recruiting - Clinical trials for Orthostatic Hypotension

Frequency of Orthostatic Hypotension in Patients Who Underwent Colonoscopy

Start date: May 1, 2024
Phase:
Study type: Observational

Patients who will undergo colonoscopy accompanied by sedoanalgesia will be admitted at Aksaray Training and Research Hospital Gastroenterology Clinic between May and July 2024. Orthostatic hypotension will be evaluated after patients meet the discharge criteria in the postoperative recovery unit.

NCT ID: NCT06439446 Completed - Cerebral Palsy Clinical Trials

Functionality and Family Characteristics in Children With Cerebral Palsy

Start date: June 6, 2023
Phase:
Study type: Observational

The aim of this study was to investigate the effect of family characteristics on functional level in children with Spastic Type Cerebral Palsy who are able to walk.

NCT ID: NCT06439186 Completed - Local Infiltration Clinical Trials

The Use of Infiltrative Anesthesia Instead of Inferior Alveolar Block

Start date: May 1, 2022
Phase: Phase 4
Study type: Interventional

Generally it is accepted that infiltrative anesthesia (IA) is not sufficient for extraction of lower molars and that an inferior alveolar nerve block (IANB) is needed. In this study, it was aimed to compare the effectiveness of IANB and IA in extraction of devitalized mandibular molars. Sixty subjects are randomly divided into study (n=30) and control (n=30) groups. Lidocaine with epinephrine is used for all injections. In the study group only vestibular and lingual IA will be used. In the control group, IANB will be applied. Teeth were extracted as usual. The pain felt during extraction will be compared.