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NCT ID: NCT06232733 Not yet recruiting - Mental Health Issue Clinical Trials

HELP (HEalthy Lifestyles Project) for Youth With Mental Distress

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

The goal of this clinical trial is to learn about how healthcare providers can support youths' mental health. The main question[s] it aims to answer are: - Do youth (12 to 17 years of age) who engage in the 6-month HELP e-intervention have a larger improvement in emotional health (measured by the Strengths and Difficulties Questionnaire) than youth who do not receive the intervention? - Does engagement in the HELP e-intervention improve lifestyle behaviour (physical activity, sleep or screen time)? - Do youth who engage in the 6-month HELP e-intervention utilize fewer mental healthcare resources, during and for 1 year following study participation, than youth who do not receive the intervention? Participants will receive the HELP intervention for 6 months, either immediately or after waiting 6 months from study enrollment. At 0, 3, 6, and 12 months, participants will answer a series of questionnaires to assess their emotional health and lifestyle behaviors. Researchers will compare the emotional health and lifestyle behaviors of youth who received HELP immediately to those who wait for 6 months prior to the intervention to see if their emotional health or lifestyle behaviors differ.

NCT ID: NCT06240676 Not yet recruiting - Health Behavior Clinical Trials

Examining the Effect of Breastfeeding Education Given to Mothers Based on Postpartum Awareness Practices on Breast Milk and Cortisol Hormone at the Newborn Circadian Level

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

In addition to being an easily accessible and ready-made food for babies in the first years of life, breast milk plays a major role in transmitting information about the time of day to newborn babies and therefore in the formation of the circadian rhythm, thanks to the hormones and various immune elements it contains.The main theme of mindfulness-based programs is mind and body meditation by focusing on the present moment, directing perception to inner experiences and observing these experiences.Regular practice of this type of meditation contributes greatly to increasing happiness and developing positive attitudes such as insight, compassion, awareness and stress management.Cortisol is the main stress hormone in the human body and is therefore a promising benchmark for investigating the effects of mindfulness programs. The purpose of mindfulness-based breastfeeding training to be given to mothers; It is to contribute to a healthy and safe postpartum period and breastfeeding experience for the mother and the newborn by minimizing the negative effects of the postpartum stress level in the mother and the cortisol hormone levels transferred from the mother's milk to the baby on the circadian rhythm.For this purpose, the sample size was planned to be a total of 54 people, 27 people per group, in the experimental design, with G power 3.1 analysis. The research will be conducted on healthy breastfeeding mothers who applied to Erzurum City Hospital and Kars Selim District State Hospital between 15.05.2023 and 15.06.2024.Subjects to be included in the study will be randomly selected among the pregnant women who applied to the clinic according to meeting the inclusion criteria. Breastfeeding: 'The Key to Sustainable Development'. For this reason, it is planned that the determination of the relationship between breast milk and circadian rhythm can be supported by cognitive methods, it will be important in terms of promoting breastfeeding and achieving development goals in a short time, and it is planned to contribute to the literature.

NCT ID: NCT06241989 Not yet recruiting - Clinical trials for Level of Digital Game Addiction

Digital Game Addiction and Cyberbullying in Adolescents

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

With the widespread use of technology and internet, digital game addiction and cyberbullying behaviors have increased among adolescents. Effective interventions are needed to prevent these behaviors. The aim of the study is to determine the effect of health education supported by motivational interviewing on digital game addiction and cyberbullying behaviors in adolescents. The research will be conducted with a randomized controlled trial design. The intervention group will receive six sessions of motivational interviewing-supported health education. Within the scope of the intervention, the first two sessions will be health education and the last four sessions will be motivational interviewing. It is planned that each session will be 35 minutes and the sessions will be implemented one week apart.

NCT ID: NCT06242574 Not yet recruiting - Alzheimer Disease Clinical Trials

Meaningful Aspects of Health for Adults With Dementia, Their Care Partners and Healthcare Practitioners

DiME
Start date: April 15, 2024
Phase:
Study type: Observational

The aim of this study is to describe, using a non-interventional survey, the relevant aspects of health in adults with ADRD for the patients themselves, their carers and healthcare professionals. Commonalities and differences between these three stakeholders and according to the severity of the dementia will also be studied.

NCT ID: NCT06247904 Not yet recruiting - Clinical trials for Tetraplegia/Tetraparesis

NIBS Therapy in Subacute Spinal Cord Injury

NIBS-SCI1
Start date: April 15, 2024
Phase: N/A
Study type: Interventional

No accepted clinical therapies exist for repair of motor pathways following spinal cord injury (SCI) in humans, leaving permanent disability and devastating personal and socioeconomic cost. A robust neural repair strategy has been demonstrated in preclinical studies, that is ready for translation to recovery of hand and arm function in human SCI, comprising daily transcranial magnetic stimulation treatment at the inpatient rehabilitation facility. This study will establish clinical effect size of the intervention, as well as safety and feasibility necessary for a subsequent controlled efficacy trial and inform preclinical studies for dosing optimization.

NCT ID: NCT06251076 Not yet recruiting - Multiple Myeloma Clinical Trials

Plan Development for Giving Teclistamab in the Outpatient Setting

Start date: April 15, 2024
Phase: Phase 4
Study type: Interventional

This is a pilot study to develop an outpatient-based process for the administration of teclistamab for for relapsed/refractory multiple myeloma patients and to evaluate the burden on caregivers of patients receiving outpatient administration of teclistamab.

NCT ID: NCT06256666 Not yet recruiting - Clinical trials for Cognitive Deterioration

Objective Measurement of Pain in Individuals With Cognitive Deterioration Utilizing Electroencephalography

Start date: April 15, 2024
Phase:
Study type: Observational

This research addresses the challenge of pain assessment in individuals with cognitive deterioration (CD), a common aspect of aging and various neurological conditions. Due to difficulties in self-reporting, especially in severe cases, accurate pain diagnosis and management are hindered. The study explores the use of electroencephalography (EEG) and machine learning techniques to objectively measure pain in CD patients. Utilizing a BIS device, the research aims to identify EEG markers associated with pain, comparing them with an objective PANAID scale. The study targets patients in surgical departments, providing valuable insights into enhancing pain assessment for those unable to express pain through traditional subjective scales.

NCT ID: NCT06258707 Not yet recruiting - Aphakia Clinical Trials

Bicentric Clinical Investigation to Assess Safety and Performance of LuxBoost IOL

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

The study purpose is to demonstrate safety and performance of bilateral implantation of LuxBoost intraocular lenses compared with the LuxGood Monofocal lens.

NCT ID: NCT06265207 Not yet recruiting - Mammography Clinical Trials

The Effect of Virtual Reality on Pain, Anxiety and Satisfaction Level Before Mammography

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

In this study, it is planned to determine the effect of virtual reality applied to women before mammography on pain, anxiety and satisfaction levels. For this purpose, individuals applying for breast cancer screening will first be randomly divided into experimental and control groups. Pain, anxiety and satisfaction level evaluation forms will be applied to the experimental group before the mammography procedure. A relaxing video will be watched with virtual reality glasses and the mammography will be performed. At the end of the mammography, the relevant forms will be applied to the individuals again. The control group will not be subjected to any additional application that will continue with the applied routine.

NCT ID: NCT06287593 Not yet recruiting - Clinical trials for EGF-R Positive Non-Small Cell Lung Cancer

The Feasibility of Dynamic Liquid Biopsy Monitoring During Neoadjuvant Treatment for EGFR-mutated NSCLC

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

This study aimed to assess the value of dynamic ctDNA monitoring in guiding the development of personalized neoadjuvant treatment strategies for EGFR-mutated NSCLC patients.