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Health Status clinical trials

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NCT ID: NCT04248478 Recruiting - Fibromyalgia Clinical Trials

Eating Behaviours in Female Patients With Fibromyalgia

Start date: January 29, 2020
Phase:
Study type: Observational

The Relationship Between Eating Behaviours and Health Status of Female Patients with Fibromyalgia

NCT ID: NCT04009564 Completed - Health Status Clinical Trials

Effect of Date Seeds Coffee on Mood and Cognitive Performance

Start date: June 20, 2019
Phase: N/A
Study type: Interventional

Limited utilizations of date seeds have previously been explored, and so previously wastage has often been the normality. However, research now indicates that several fruit seeds contain higher concentrations of beneficial total phytochemicals within their seeds in comparison to the flesh. As well as high nutritional values of date seeds for fibre, protein and micronutrients, this increased phytochemical content has been proven to be true for date seeds, with mainly phenolic acids (24.6 g k GAE) 3 and total flavonoids (3.67 g k RE). With the seeds presently being used to produce new coffee products, it raises questions on whether consumption of date seeds can alter mood and cognitive behaviour and therefore research into investigate the acute effect of date seeds coffee on mood and cognitive function on healthy young volunteers. However, to the best of the research team knowledge, this is the first human trial to investigate these effects.

NCT ID: NCT03429231 Completed - Health Status Clinical Trials

Observational Study to Evaluate the Quality of Life of Healthy Postmenopausal Women Who Take Coenzyme Q-Ubiquinol

Start date: November 23, 2017
Phase:
Study type: Observational

Observational study about quality of life in postmenopausal women taking coenzyme Q compared to another group of women of the same age who do not take it

NCT ID: NCT03254537 Enrolling by invitation - Health Status Clinical Trials

Effect of Mediterranean Diets Based on Organic and Conventional Foods

Start date: May 1, 2017
Phase: N/A
Study type: Interventional

Results from a small number of human cohort studies are also available and indicate that there are positive associations between organic food consumption and reduced risk/incidence of certain acute diseases (e.g. pre-eclampsia, hypospadias) and obesity/overweight. Results from animal dietary intervention studies suggest that (i) switching to organic food consumption results in significant changes in hormonal balances and an increase in immune system responsiveness and (ii) differences in pesticide residue, cadmium, protein and antioxidant concentrations between organic and conventional foods are major drivers for hormonal balances and immune system parameters in animals. However, there is virtually no published data from (i) long-term cohort studies focusing on chronic diseases (e.g. cardiovascular disease, diabetes, cancer and neurodegenerative conditions) and (ii) controlled human dietary intervention studies comparing effects of organic and conventional diets. It is therefore currently not possible to assess whether and estimate to what extent organic food consumption may affect human health.

NCT ID: NCT02663037 Completed - Health Status Clinical Trials

Simple Segmentation Tool to Understand Elderly Health Status and Needs

Start date: May 2016
Phase: N/A
Study type: Observational

Background: The delivery of targeted, patient-centered care for a population with heterogeneous healthcare needs while moderating costs is a key challenge in healthcare. Segmentation of patient populations based on clinically distinguishing features and social healthcare needs is currently a promising method for informing the organization of healthcare supply to these needs. Aims: In this prospective cohort study, the investigators aim to assess the Simple Segmenting Tool (SST) as a method of patient population segmentation in terms of its inter-rater reliability, as well as convergent and predictive validity. We will also revise the tool based on feedback from the validity studies should the need arises. Hypothesis: The investigators hypothesize that the SST is able to exhibit good inter-rater reliability, convergent validity and predictive validity for adverse events. Methodology: Non-critical patients aged 55 and above presenting to the Emergency Department will be screened with the SST. Raters will be paired in order to assess inter-rater reliability. To test convergent validity, the LACE, SF-12, and Clinical Frailty Scale (CFS) will also be used. Finally, predictive validity will be assessed by evaluating adverse event rates of patients in each SST category. Adverse events include all-cause mortality, length of hospital stay, emergency department visit and unplanned hospital readmission. Significance to Health Services Delivery: This study will provide evidence supporting the use of a standardized tool for evaluating the medical and social needs of patients at various sites of care. Following which, tailored packages of healthcare services can then be delivered in order to meet these needs.

NCT ID: NCT02297646 Completed - Health Status Clinical Trials

Influencing Factors on Training Efficacy in Healthy Adults

CHO
Start date: August 2012
Phase: Phase 0
Study type: Interventional

The purpose of this study is to investigate the effects of carbohydrate intake on training efficacy and health parameters of an endurance training program in healthy adults.

NCT ID: NCT01171222 Completed - Stress Clinical Trials

Health Status and Cardiovascular Stress of Veteran Soccer Players

Start date: March 2010
Phase: N/A
Study type: Observational

This study shall provide missing descriptive data on health status of veteran players and potential preventive effects of soccer at an age of 40 to 60 years. The investigation represents a cross-sectional examination of cardiovascular parameters and metabolic stress induced by training and competition. Additionally, orthopedic and other medical risks are to be revealed, and options should be developed to minimize these risks, e.g. by preventive measures included in training or rule modifications.

NCT ID: NCT00977847 Completed - Family Research Clinical Trials

Integrating Patient Generated Family Health History From Varied Electronic Health Record (EHR) Entry Portals

Start date: November 2010
Phase: N/A
Study type: Interventional

In the 21st century, the importance of family health history will increase as it will be essential to put detailed personal genetic information into the context of an individual's health, namely the context of how the shared code has played out in an individual and his/her closest relatives. These scientific developments in the investigators' understanding of genetics will demand a more comprehensive family history dataset for all patients, and the time limitations on healthcare providers demand a technology-driven solution that integrates an individual's knowledge of their family history with the medical records maintained by their health care providers. A solution does not currently exist by which most Americans can organize their family health history and then place it into their electronic health record (EHR). The investigators propose to develop and compare three different ways of proactively collecting family history information from patients using computer technology independent of a health care visit, including telephone (interactive voice response technology), tablet computers in a physician's waiting room, and a secure internet portal at home. These tools will be based on the US Surgeon General's My Family Health Portrait, an electronic family history collection tool. Family history data will be transferred and integrated with a patient's EHR in a large primary care network. This project will seek to demonstrate that family history data can be accurately reported by diverse patients using these technologies, and that these data can be integrated to tailor an individual's health care based on their familial risk.

NCT ID: NCT00940355 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Secondary Prevention of Problems in Health Status in Patients With Chronic Obstructive Pulmonary Disease (COPD)

Start date: September 2007
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the effectiveness of an intervention conducted by a pulmonary nurse in patients with COPD. The hypothesis is that in a sample of COPD patients with clinically relevant problems in health status (physiological functioning, symptoms, functional impairment and quality of life), a motivational intervention conducted by a pulmonary nurse will lead to patient-tailored treatment and an improved health status.

NCT ID: NCT00537706 Completed - Health Status Clinical Trials

Choosing Healthful Interventions

Start date: September 21, 2007
Phase: N/A
Study type: Observational

This study will identify what programs, along with traditional healthcare, low-income urban residents would choose to improve their health. The information is intended as a step toward designing public policies aimed at improving the health of low-income populations in the United States. Residents of Washington, D.C., who are between 18 and 64 years of age and are in a specified income bracket may be eligible for this study. Participants take part in audio-taped group discussions led by a trained facilitator. During a 3 hour session, participants engage in 4 cycles of choosing benefits. Participants select benefits as follows: - For themselves individually. - For their neighborhood. - For an entire city. - Once again individually.