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NCT ID: NCT05850403 Completed - Social Media Clinical Trials

Social Media Impact on Patients' Regarding Aesthetic Dental Treatments

Start date: March 21, 2023
Phase:
Study type: Observational [Patient Registry]

The aim of this observational study was to describe dental patients the use of social media related to aesthetic dental treatments. The main questions it aims to answer were: - Describe the use of social media before undergoing an aesthetic treatment. - To assess the influence of social media prior to undergoing aesthetic treatment Participants answered a web-base questionnaire.

NCT ID: NCT05849792 Completed - Depression Clinical Trials

Internet-based Physical Activities Randomized Controlled Trial in Mild/Moderate Depression Participants: SONRIE Project

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

The goal of this randomized controlled trial is to determine the effect of an intervention program with physical activity for 12 weeks on depression, social and emotional well-being and quality of life and health in adults with mild and moderate depression. The main questions it aims to answer are: 1. - To determine the association of physical activity levels, sedentary behavior, sleep patterns, physical condition, diet, and general health status with mental and social well-being, and quality of life in a large sample of adult patients diagnosed with mild or moderate depression. 2. - To examine the predictive capacity of physical activity, sedentary behaviors, and physical condition on mild and moderate depressive disorder. 3. - To study the effect of a period without an intervention program with physical activity (8 weeks without exercise intervention) on the variables studied. 4. - To examine the role of the endocannabinoid system on depression as well as its behavior after an intervention program of physical activity. Participants will be involved in a physical activity intervention program for 12 weeks. Researchers will compare intervention group and control group to see if an intervention program with physical activity for 12 weeks improve depression, social and emotional well-being and quality of life and health in adults with mild and moderate depression.

NCT ID: NCT05848518 Completed - Long COVID Clinical Trials

Exercise for Health in Patients With Post-acute Sequelae of COVID-19

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

Background: Many patients with COVID-19 present the so-called post-acute sequelae of COVID-19 such as fatigue, post-stress discomfort, dyspnea, headache, pain mental impairment, incapacity to perform daily physical tasks ant exercise intolerance. This study aims to investigate the effects of different exercise programs on physical and mental fitness, physical condition and biomarkers of the immune system and oxidative stress in older COVID-19 survivors. Methods: The sample will be made up of 120 eligible participants, over the age of 60 years who have had COVID-19 disease and are survivors and present persistent COVID-19 symptomatology diagnosed by the corresponding physician. The participants will be randomly assigned to the experimental groups: supervised endurance group (SEG, n = 30), supervised strength group (SSG, n = 30), supervised concurrent group (SCG, n = 30), which will perform the corresponding exercise program 3 days a week compared to the control group (CG, n = 30), which will not carry out a supervised exercise program. The design of this project will include assessment of cardiorespiratory fitness, muscle fitness, pain and mental health, and biomarkers of inflammation and oxidative stress.

NCT ID: NCT05847972 Completed - Clinical trials for Ankle Injuries and Disorders

Effect of Manual Therapy and Inmediately Application of Plantar Orthoses

Start date: June 6, 2023
Phase: N/A
Study type: Interventional

Limitation of ankle dorsiflexion is directly related to pronated foot. For its treatment, plantar orthoses and manual therapy are used. There is a lack of evidence on their combination, as to when the cast should be taken after manipulation. Our hypothesis proposes that it is more effective to cast immediately after manipulation.

NCT ID: NCT05847374 Completed - Sleep Clinical Trials

Effect of Asynchronies on Sleep Disruption During Mechanical Ventilation

SleepUCI
Start date: January 1, 2019
Phase:
Study type: Observational

Mechanically ventilated (MV) patients in the Intensive Care Unit (ICU) are highly susceptible to sleep disruption. Several studies in the last 15 years have demonstrated an extremely poor sleep quality and abnormal sleep pattern evaluated by polysomnography (PSG) devices (the gold standard method for evaluating sleep quality and quantity). Patient-ventilator interaction is frequently poor leading to asynchronies of varied type and consequences. Moderate-to-severe asynchronies are associated with longer mechanical ventilation, weaning failure and mortality. The goal of this study is to look for an association between poor sleep quality and patient-ventilator asynchronies. This study is an observational, physiological study investigating sleep quality and quantity in MV patients by recording portable PSG (from 22:00 to 08:00) at night while continuously monitoring 24h/day of patient-ventilator interaction (BetterCare system).

NCT ID: NCT05844189 Completed - Dyspareunia; Female Clinical Trials

Physiotherapy Treatment With Capacitive Resistive Monopolar Radiofrecuency in Young Women With Dyspareunia

[CRMRF]
Start date: November 5, 2021
Phase: N/A
Study type: Interventional

The hypothesis of this study is that capacitive-resistive monopolar radiofrecuency (CRMRF) with vaginal manual physiotherapy improves sexual health in young women suffering from dyspareunia (pain during sexual intercourse). The realization of studies that help to know the therapeutic possibilities in the field of dyspareunia seems necessary, taking into account the number of women affected, as well as the deficits of scientific evidence in this field. The main objective of this study is to analyze whether the use of CRMRF brings additional benefits to the results of manual therapy on dyspareunia in young women. Likewise, it intends to analyze the data for two secondary objectives: 1. Analyze changes in different areas of women's sexual function in young people with dyspareunia through treatment (Desire, arousal, lubrication, orgasm, satisfaction and pain). 2. Study if the use of CRMRF is an added benefit in personal perception while receiving treatment.

NCT ID: NCT05843513 Completed - Dental Wear Clinical Trials

Tooth Wear Monitoring Using Intraoral Scanner

Start date: January 18, 2019
Phase:
Study type: Observational

The overall objective was to evaluate the monitoring of tooth wear using the intraoral scanner. Forty-six participants were selected according to the established inclusion and exclusion criteria. Monitoring of tooth wear, evaluation of possible aetiological factors, as well as patient satisfaction with the use of the intraoral scanner were carried out.

NCT ID: NCT05842655 Completed - Clinical trials for Dental Prosthesis Failure

Digital Technique to Analyze the Wear of Implants and Natural Tooth as Antagonist.

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

The aim of this study was to describe a novel digital technique to analyze the wear of screw-retained implant-supported metal-ceramic dental prostheses and natural tooth as antagonist. Materials and methods: Ten patients were consecutively included to rehabilitate partial edentulism by dental implants. Both the screw-retained implant-supported metal-ceramic dental prostheses and the natural tooth as antagonist were submitted to a digital impression through an intraoral scan to generate a Standard Tessellation Language digital file preoperatively (STL1), at 3 months (STL2), and 6 months (STL3) follow-up. Afterwards, an alignment procedure of the digital files (STL1-STL3) was performed on a reverse engineering morphometric software and volume changes at the screw-retained implant-supported metal-ceramic dental prostheses and the natural tooth as antagonist were analyzed using Student's t-test. Moreover, Gage R&R statistical analysis was conducted to analyze the repeatability and reproducibility of the digital technique.

NCT ID: NCT05842642 Completed - Migraine Clinical Trials

Effects of Adding an Oculomotor Therapy Treatment in Patients With Migraine

Start date: April 3, 2023
Phase: N/A
Study type: Interventional

Headaches are the fourth cause/reason for disability in the world population. Of which, headache in general accounts for 47%, 38% are tension headaches, 10% migraines and 3% for chronic headache lasting more than 15 days a month. Migraine is a neurological disease/disorder originating in the central nervous system with difficulty modulating responses to common sensory stimuli. Different studies have linked possible oculomotor problems and headaches, being an important and complex relationship. It is difficult to find a suitable and beneficial treatment for the treatment of migraine. It is hypothesized that adding a treatment of manual therapy and therapeutic exercise of the oculomotor system to an already established protocol of manual therapy and therapeutic exercise of the cervical region, has an additional benefit for patients with migraines (in relation to the quality of life, symptomatology and functionality).

NCT ID: NCT05837741 Completed - Cancer Clinical Trials

Leucine-enriched Formulas in Patients With Tumor-induced Sarcopenia

Start date: March 1, 2021
Phase: N/A
Study type: Interventional

Currently there is a lack of evidence for recommending specific oral supplements (OS) for nutritional support in patients with cancer, including leucine-enriched supplements.