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NCT ID: NCT06394960 Recruiting - Clinical trials for Systolic Blood Pressure (20% or Greater Increase)

Factors Predicting Blood Pressure Change With Interscalene Block

Start date: May 2, 2024
Phase:
Study type: Observational

The primary aim of this study is to identify potential anthropometric features that predict the relationship between the Interscalene Block procedure and changes in blood pressure

NCT ID: NCT06394726 Recruiting - Dysmenorrhea Clinical Trials

Examining the Impact of Aerobic and Core Exercises on Primary Dysmenorrhea in High School Females

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

Dysmenorrhea, derived from ancient Greek, translates to 'difficult monthly flow' and refers to painful cramps during menstruation, a common cause of pelvic pain. The pain, often in the lower abdomen, results from uterine pressure exceeding 60 mmHg. Symptoms include suprapubic pain, radiating discomfort, nausea, diarrhea, and headache, impacting quality of life. Etiology involves factors like age at menarche, heavy flow, lifestyle, and medical conditions. Dysmenorrhea is categorized as primary (without underlying pathology) or secondary (due to conditions like endometriosis). Its prevalence is high in adolescence, affecting daily life, school, and health. Research aims to assess how aerobic and core exercises influence pain and quality of life in adolescent females (14-18 years). Participants are randomly assigned to study and control groups, exploring the potential benefits for health, well-being, and academic performance.

NCT ID: NCT06394648 Recruiting - Clinical trials for Geriatric Individuals

Investigation of Sarcopenia and Physical Fitness Levels of Geriatric Individuals Living in Nursing Homes and at Home

Start date: April 5, 2024
Phase:
Study type: Observational

To examine the sarcopenia and physical fitness levels of geriatric individuals living in nursing homes and at home. Considering these aims, our working hypotheses are; H1: There is a difference in sarcopenia level between geriatric individuals living in a nursing home and at home. H2: There is a difference in dynapenia levels between geriatric individuals living in a nursing home and at home. H3: There is a difference in physical fitness between geriatric individuals living in a nursing home and at home.

NCT ID: NCT06394635 Recruiting - Chronic Stroke Clinical Trials

Use of Plantar Flexion Resistant Ankle-Foot Orthosis in Stroke Patients With Genurecurvatum Gait

Start date: March 22, 2024
Phase:
Study type: Observational

Hypothesis 1: Ho: Ankle-foot orthosis, which fixes the ankle at different angles (3 degrees dorsiflexion - 5 degrees dorsiflexion), has no effect on knee hyperextension control in stroke patients with genurecurvatum gait. H1: Ankle-foot orthosis, which fixes the ankle at different angles (3 degrees dorsiflexion - 5 degrees dorsiflexion), has an effect on knee hyperextension control in stroke patients with genurecurvatum gait. Hypothesis 2: Ho: Ankle-foot orthosis, which fixes the ankle at different angles (3 degrees dorsiflexion - 5 degrees dorsiflexion), has no effect on pelvic movements in stroke patients with genurecurvatum gait. H1: Ankle-foot orthosis, which fixes the ankle at different angles (3 degrees dorsiflexion - 5 degrees dorsiflexion), has an effect on pelvic movements in stroke patients with genurecurvatum gait.

NCT ID: NCT06393062 Recruiting - Clinical trials for Percutaneous Nephrolithotomy

Gram Stain of the First Urine After Puncture in Percutaneous Nephrolithotomy

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

In this study, investigators compared the systemic inflammatory responses after percutaneous nephrolithotomy (PCNL) patients who were given an expanded empirical antibiotic regimen based on the prediction of the possibility of bacteria identified by Gram staining the first urine after renal puncture and patients whose antibiotic regimen was not performed and whose antibiotic regimen was adjusted according to patient symptoms and culture results. Investigators aimed to test its diagnostic value in predicting and preventing complications.

NCT ID: NCT06393010 Recruiting - Tele-rehabilitation Clinical Trials

The Effect of Online Rehabilitation Applications on Pain and Quality of Life in Textile Workshop Workers

Start date: May 7, 2024
Phase: N/A
Study type: Interventional

Musculoskeletal problems are a common health issue among individuals working in textile workshops, attributed to factors such as ergonomic risks in working conditions, personal characteristics of employees, and other workplace factors. Neck pain, back pain, shoulder pain, wrist pain, hand and finger pain, knee pain, and foot pain are frequently observed issues among those working in textile workshops, negatively impacting their functionality and quality of life. The research aims to investigate the effects of online rehabilitation education on pain and quality of life among textile workers. Participants aged between 21 and 52 working in textile workshops will be included in the study. All participants will be evaluated twice, before and after treatment, with all assessments conducted face-to-face. Demographic information such as age, gender, marital status, etc., will be assessed using a structured socio-demographic form. Pain levels will be assessed using the 100 mm VAS, quality of life will be assessed using the SF-36 questionnaire, and posture evaluation will be conducted using anterior and lateral posture analysis. The rehabilitation program administered to participants will take place over a period of 3 months, with sessions conducted three times a week on an online platform. The rehabilitation program will include posture exercises, stretching exercises, exercises for normal joint range of motion, strengthening exercises, regional pain education (shoulder, elbow, hip, wrist), and discussions on good and poor posture, lasting approximately 40-45 minutes.

NCT ID: NCT06392984 Recruiting - Pectus Excavatum Clinical Trials

Ultrasonographic Measurement of Diaphragmatic Thickness in Adolescents With Pectus Deformity

Start date: February 21, 2024
Phase:
Study type: Observational

Pectus deformities are among the most common anterior chest wall pathologies. Pectus excavatum is the most common chest deformity with an incidence of 0.1-0.3%. In severe deformities, a decrease in lung volume is observed. This can cause decreased pulmonary function and affect the function of the right ventricle. The diaphragm is the main respiratory muscle, and diaphragm contraction is associated with respiratory functions. So, investigators aimed to measure diaphragmatic thickness in adolescents with pectus deformity and to show whether diaphragmatic thickness is an early predictor of respiratory disorder in participants who do not show any clinical symptoms or whose respiratory functions are normal.

NCT ID: NCT06392880 Recruiting - Health, Subjective Clinical Trials

Comparison of Floss Band Application and Mulligan Mobilization

Start date: February 14, 2024
Phase: N/A
Study type: Interventional

This study will investigate the effects of Floss band application and Mulligan mobilization on ankle range of motion, vertical jump, gait and balance in active healthy young adults.

NCT ID: NCT06392620 Recruiting - Clinical trials for Ankylosing Spondylitis

Telerehabilitation in Ankylosing Spondylitis

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

Ankylosing Spondylitis (AS) is an inflammatory rheumatic disease primarily affecting the spine and sacroiliac joint. xercise is one of the most important nonpharmacologic treatment modalities in AS. Stretching, strengthening, aerobic, posture, balance and moltimodal exercise methods are the most commonly used treatment methods. The study will include 44 patients diagnosed with AS aged 18-65 years. Patients will be divided into two randomized controlled groups with 22 patients in each group. Group 1 will receive a personalized exercise program including stretching, strengthening, respiratory, aerobic and posture exercises via video conferencing. Group 2 will be recommended a video on the YouTube platform and will be asked to perform the exercises by following the content of these videos. Spinal mobility will be assessed with Bath Ankylosing Spondylitis Metrology Index, disease activity with Bath Ankylosing Spondylitis Disease Activity Index, function with Bath Ankylosing Spondylitis Function Index, quality of life with Ankylosing Spondylitis Quality of Life Scale and posture with PostureScreeen mobile application.

NCT ID: NCT06392256 Recruiting - Clinical trials for Peri-implant Mucositis

Effect of Free Gingival Grafting on Peri-implant Health

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

The goal of this randomized-controlled clinical study is to investigate the impact of soft tissue phenotype modification following free gingival grafting (FGG) in addition to the non-surgical mechanical therapy of peri-implant mucositis (PM) with keratinized mucosa width (KMW) < 2 mm over a 6-month follow-up period. Therefore, the following questions related to the study are raised: - Does soft tissue modification following free gingival grafting around the implants, in addition to non-surgical mechanical therapy of PM, affect the complete disease resolution? - Does the presence of KMW < 2 mm around the implants exhibit similar outcomes compared to the sites with sufficient KMW (i.e., ≥ 2 mm) for professional mechanical plaque removal? Patients who apply to the Department of Periodontology, Faculty of Dentistry, Gazi University, are systemically healthy, have implant-supported fixed restorations installed at least one year prior to their enrollment, and are diagnosed with PM on these implants will be selected for the study. Patients with KMW < 2 mm at the respective implant sites will be treated with non-surgical mechanical treatment combined with soft tissue augmentation with FGG or non-surgical mechanical treatment alone. As a positive control group, those who apply to the same department, have implants in function as noted during routine annual maintenance appointments, and are diagnosed as healthy will be selected.