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NCT ID: NCT04717492 Completed - Clinical trials for Pulmonary Disease, Chronic Obstructive

An Observational Study of Beta-Blocker Use in Patients With COPD and Acute MI

BLOCK2
Start date: June 28, 2020
Phase:
Study type: Observational

The study is a prospective, observational study of patients admitted to the BLOCK COPD network hospitals with acute AMI and COPD to determine the prevalence of COPD in patients admitted to the hospital with an acute myocardial infarction (AMI) and to characterize the phenotypic expression and severity of their underlying lung disease. Patients with will be identified via the EMR. 571 participants will be enrolled.

NCT ID: NCT04717401 Completed - Clinical trials for Sacroiliac Joint Somatic Dysfunction

Comparison Between Strain-counterstrain and Muscle Energy Technique in Sacroiliac Joint Dysfunction

Start date: August 8, 2020
Phase: N/A
Study type: Interventional

Examine the effect of strain-counter strain (SCS) versus muscle energy technique (MET) on pain pressure threshold (PPT), functional disability, and the innominate angle tilt with SIJ dysfunction.

NCT ID: NCT04717076 Completed - Clinical trials for Reduction of Cardiovascular Risk Factors

PrevA Study - Evaluation of an App-based Nutritional Concept

PrevA
Start date: April 12, 2021
Phase: N/A
Study type: Interventional

The PrevA study is designed to evaluate our developed nutritional concept to implement a heart healthy diet. The nutritional concept based on nutrient-optimized daily menu plans for each study day. The plans are personalized according to participants age, gender, and level of physical activity. The PrevA study consists of four periods differing in the energy intake specified by the menu plans. The study is carried out in a 4-armed parallel design. In group 1, the participants receive the individualized daily plans via the app coupled with the smartwatch to record participants physical activity and heart rate. Groups 2 and 3 receive a printed version of the daily plans with or without personal nutritional advice. The fourth group serves as a control group, which receives general nutritional recommendations but no daily menu plans. During this time, blood samples and urine are collected every four weeks to analyze the study parameters.

NCT ID: NCT04716920 Completed - Clinical trials for Anatomic Stage III Breast Cancer AJCC v8

Tai Chi for Relieving Aromatase Inhibitor-Induced Arthralgia in Patients With Stage I-III Breast Cancer, the TaiChi4Joint Trial

Start date: March 11, 2020
Phase: N/A
Study type: Interventional

This trial studies new methods using Tai Chi for the relief of joint pain (arthralgia) caused by an aromatase inhibitor in patients with stage I-III breast cancer. Tai Chi is a mind-body therapy that integrates moderate physical activity, deep breathing and meditation. Tai Chi may help to reduce aromatase inhibitor-induced joint pain, and offer a promising approach to managing symptoms in cancer patients.

NCT ID: NCT04715724 Completed - Breastfeeding Clinical Trials

Comparison of Baby Dolls for Teaching Newborn Positioning and Attachment

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

In this baby doll comparison study, clinical lactation specialists will complete two back-to-back video-based simulations (telesimulations) focused on newborn positioning and attachment. Study participants will interact with a standardized patient educator (SP) wearing the Lactation Simulation Model and using two baby dolls in a randomized order.

NCT ID: NCT04715516 Completed - Clinical trials for Health Knowledge, Attitudes, Practice

Increasing Knowledge of Alcohol as a Risk Factor for Breast Cancer Among Women Attending Breast Screening Services

Health4Her
Start date: February 5, 2021
Phase: N/A
Study type: Interventional

Alcohol is a major modifiable risk factor for breast cancer in women, yet this is not widely understood by health practitioners or policy makers, let alone the general population. The investigators aim to test the effects of a targeted alcohol and lifestyle brief intervention for women attending breast screening services, to improve knowledge of alcohol as a risk factor for breast cancer and reduce harmful alcohol use.

NCT ID: NCT04715282 Completed - Clinical trials for Benign Paroxysmal Positional Vertigo

The Epley Maneuver Versus Cawthorne-Cooksey Exercises in the Treatment of Benign Paroxysmal Positional Vertigo (BPPV)

BPPV
Start date: March 2016
Phase: N/A
Study type: Interventional

Observation of the effects of Cawthorne-Cooksey exercises applied after the Epley maneuver on balance, vertigo symptoms, and quality of life in BPPV patients.

NCT ID: NCT04714736 Completed - Clinical trials for Acute Coronary Syndromes

DyeVert System and Contrast-induced Acute Kidney Injury

REMEDIALIV
Start date: February 10, 2020
Phase: N/A
Study type: Interventional

The aim of the REnal Insufficiency Following Contrast MEDIA Administration TriaL IV (REMEDIAL IV) is to test whether the use of the DyeVert system is effective in reducing CI-AKI rate in ACS patients undergoing urgent/immediate (within 2 hours) invasive diagnostic and/or interventional cardiovascular procedures. The DyeVertâ„¢ system (Osprey Medical Inc., Minnetonka, MN, USA) is a novel device designed to reduce CM volume during coronary procedures, while maintaining fluoroscopic image quality. Patients with ACS scheduled for urgent/immediate coronary angiography/angioplasty will be enrolled and randomized into 2 groups: 1) DyeVert group (CM injection will be handled by the DyeVert TM system), and 2) Control group (CM injection will be carried out by a conventional manual injection syringe).

NCT ID: NCT04714242 Completed - Clinical trials for Polypoidal Choroidal Vasculopathy

OCTA and Polypoidal Choroidal Vasculopathy

Start date: January 15, 2019
Phase:
Study type: Observational

To investigate the structural and vascular features of choroid in patients affected by PCV after Ranibizumab intravitreal injection.

NCT ID: NCT04713020 Completed - Clinical trials for Effectiveness of Application Education Intervention

Application of Educational Intervention on the Knowledge, Depression and Self-efficacy of Patients With Cerebrovascular Accident

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

Within 6 months after the occurrence of stroke, more than 25% of patients will experience severe disability. Patients and caregivers need to learn stroke self-care knowledge. Nursing personnel play the role of educator and provide self-care health education content. Traditional nursing instructions are mainly provided using leaflets and verbal health education. However, the advancement of information technology and the popularization of mobile network 3C products make it possible to provide real-time, individualized and large-capacity information, which is the most real-time and efficient way of clinical care at present. Therefore, this study investigated whether mobile device health education program provided for patients with stroke can improve their self-care knowledge and self-efficacy and reduce depression. This study enrolled patients at the wards of Division of Neurology in a certain medical center in the northern Taiwan. This study adopted two-group, pre-and-post-test, randomized, single-blind experimental research design, and calculated the samples size using G-Power. At least 35 subjects should be enrolled in the experimental group (APP education program intervention) and control group (conventional nursing), respectively. This study performed the pre-test on Day 1 of hospitalization, implemented the interventional program on Day 2, and performed the post-test before discharge. The research questionnaires included Stroke Self-care Knowledge Scale, Stroke Self-efficacy Scale, Beck Depression Inventory (BDI), VAS Health Education Satisfaction Scale. This study performed statistical analysis using the package statistical software version SPSS 20.0, and tested the distribution and homogeneity of two groups of data using the independent sample T-test. Moreover, this study also performed descriptive statistical analysis and inferential statistical analysis. For the descriptive statistical analysis, this study presented the demographic data and disease characteristics of the research subjects using frequency distribution, percentage, average mean, standard deviation, maximum and minimum. Furthermore, this study used independent sample T-test, chi-square, One-way ANOVA, Pearson product-moment correlation coefficient, and ANCOVA to compare the differences in demographic data, disease characteristics, stroke self-care knowledge, stroke self-efficacy, depression, and health education satisfaction between the two groups.