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NCT ID: NCT06179914 Completed - Childhood Cancer Clinical Trials

Resilience Models in Adolescence and Youth With Cancer in Taiwan

Start date: November 2, 2020
Phase:
Study type: Observational [Patient Registry]

Validation of Resilience Models about Cancer in Adolescence and Youth in Taiwan

NCT ID: NCT06176404 Completed - Clinical trials for Cognitive Impairment

Stellate Ganglion Block in Patients With Cerebral Small Vessel Disease

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

A prospective study was conducted on 84 CSVD patients with dysphagia and cognitive impairment. They were divided into the comparison group and observation group evenly. All the patients were provided with routine therapy, while the patients in the observation group were given SGB. The swallowing function, cognitive function and activities of daily living of the two groups of patients before and after treatment were evaluated by Penetration-Aspiration Scale, Mini-mental state examination and modified Barthel index.

NCT ID: NCT06175260 Completed - Healthy Clinical Trials

Investigation on the Efficacy of Oral Carnitine Challenge Test Based on a Gut Microbiota Functional Test

Start date: June 5, 2019
Phase:
Study type: Observational

This study seeks to enlist healthy volunteers to form a validation cohort. The purpose is to confirm the observed correlations between the gut microbiome and the capacity to produce trimethylamine N-oxide (TMAO), which will be assessed using the oral carnitine challenge test (OCCT).

NCT ID: NCT06167122 Completed - Clinical trials for Craniofacial Fibrous Dysplasia

Treatment Protocol and Long-Term Outcomes in Craniofacial Fibrous Dysplasia

CFD
Start date: March 1, 2020
Phase:
Study type: Observational

Craniofacial fibrous dysplasia (CFD) is a nonneoplastic disease characterized by fibro-osseous lesions in the affected bones. Treatment is mainly surgical and is stratified based on four different anatomical zones. This study aimed to evaluate the long-term outcomes and refine the algorithm for CFD.

NCT ID: NCT06167031 Completed - Child Abuse Clinical Trials

Chatbot Facilitated Education on Child and Adolescent Abuse

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

Background: Child and adolescent abuse and neglect (CAAN) cases are increasing both in Taiwan and worldwide. As the first healthcare professionals who come in contact with CAAN cases, nurses play a crucial role. Studies show that the lack of professional knowledge and ability of nursing staff on CAAN affects the effectiveness of timely identification and notification. Therefore, it is extremely important to improve the knowledge and ability of nursing staff to assess and report CAAN. With advancements in technology, continuing education for nurses is now more extensive than traditional lecture teaching. Online education, which breaks down the barriers of time and space in learning, has thrived after the COVID-19 pandemic. Chatbots are an option for individual learning and can increase accessibility and convenience for nurses learning how to recognize and report CAAN. Objective: The aims of the study are to evaluate the effectiveness of using chatbots as teaching aids to assist nursing personnel in preventing child abuse. This evaluation will be the impact of learning on CAAN competency. Method: The study utilizes an experimental design in which participants are purposively sampled and subsequently randomized into either the experimental or control group. The experimental group will use "chatbot" to facilitate teaching. The control group only receives lecture-based teaching. The course content is comprised of two main subjects: "CAAN" and "Nurses' Roles and Functions in CAAN," which was developed using the ADDIE model. The study employs the CAAN Knowledge and Competency Scale which retrieves from the Child abuse report intention scale (CARIS) by Feng and Wu (2005). Additionally, the learning effect is assessed at three different time points: before the course, one week after, and four weeks after. Expected Results: The study predicts that the learning effects of the experimental group, which used chatbots, will be better than those of the control group. It is expected that these results will be able to implement in various educational fields, including CAAN and interdisciplinary teams.

NCT ID: NCT06165796 Completed - Cataract Senile Clinical Trials

The Effect of LASIK on the Calibration of IOL Formula Calculation: a Comparative Study

Start date: January 1, 2022
Phase:
Study type: Observational

Direct comparison study between previous LASIK or non-LASIK cataract eyes, the performance between non-LASIK and LASIK patients were (i) Ophthalmic examinations: UDVA, CDVA and uncorrected near visual acuity (UNVA) (40cm) and (ii) Refractive prediction error: defined as difference between postoperative sphere and target refraction.

NCT ID: NCT06151327 Completed - Pressure Injury Clinical Trials

Alternating Pressure Air Mattress and Pressure Injury Prevalence

APAM
Start date: October 20, 2023
Phase:
Study type: Observational

explore the correlation of accurate implementation of APAM and pressure injury prevalence

NCT ID: NCT06136975 Completed - Vaginal Atrophy Clinical Trials

Low-level Laser Therapy for Genitourinary Syndromes and Stress Urinary Incontinence

Start date: September 30, 2022
Phase:
Study type: Observational

Genitourinary syndrome of menopause (GSM) and stress urinary incontinence (SUI) are common for women. Low-level laser therapy (LLLT) was applied for wound healing, but there was no study regarding treatment effect of GSM and SUI. This retrospective study aims to assess the efficacy of LLLT in alleviating GSM and SUI.

NCT ID: NCT06136338 Completed - Anxiety Clinical Trials

A Pilot Study of Mindfulness Intervention to the Timing of Labor Admission, Uncertainty and Anxiety

MI
Start date: March 23, 2020
Phase: N/A
Study type: Interventional

The goal of this quasi-experienmental study is to investigate the effectiveness of mindfulness-based intervention in the level of uncertainty and anxiety, and determintation towards hospital admission among pregnant women. The main questions : • Do pregnant women in intervention group reduce anxiety and uncertainty? • Do pregnant women in intervention group increase self-determintation ability towards hospital admission? Women in the intervention group participated 4 weeks mindfulness-based intervention online courses, Researchers have seen effectiveness of mindfulness-based intervention in the level of uncertainty, anxiety, and determintation towards hospital admission among pregnant women.

NCT ID: NCT06133205 Completed - Acupuncture Clinical Trials

Efficacy of Abdominal Catgut Embedding Combined With Auricular Acupressure Therapy for Obese Patients

Start date: December 9, 2021
Phase: N/A
Study type: Interventional

Objective: obesity is an important risk factor of chronic diseases, which not only threatens people's health, but also an important topic of public health. The purpose of this study is to define obesity according to the norms of the World Health Organization, and to explore whether combined weight loss methods have an impact on weight loss. Methods: In this study, Combined treatment of abdominal acupoint catgut embedding was combined with auricular pellet acupressure, The wire used for catgut embedding in the experiment was polydioxanone (PDO) 。 This experiment was divided into two groups: the experimental group A and the control group B 。 The reference measurement basis is the data obtained by "Inbody" instrument, including height and weight, body mass index (BMI), basic metallic rate (BMR), Body Fat Percentage BFP) , waist hip ratio and the data of total cholesterol (TC) and triglycerides (TG) obtained from biochemical blood examination, through the comparison before and after the test, we can judge whether the method of this test can achieve a certain degree of curative effect on weight loss.