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261. Healthy Life for Frail Malnourished Seniors Performed Together With Trained Lay Buddies

and body composition and chronic inflammation of buddies and frails are recorded before the intervention, after 10-12 weeks, and after 6 and 12 months. Discussion: To the investigators knowledge this trial is the first of its kind to provide nutrition and physical activity intervention to malnourished, frail, community-dwelling subjects by trained lay buddies, in which the health status of buddies is also expected to improve. This study assesses the effectiveness of such an intervention. If successful (...) Training in Malnourished, Frail, Community-dwelling, Elderly Subjects Carried Out by Trained Lay "Buddies" Study Start Date : January 2014 Actual Primary Completion Date : December 2015 Actual Study Completion Date : December 2015 Resource links provided by the National Library of Medicine related topics: Arms and Interventions Go to Arm Intervention/treatment No Intervention: cognitive training Participants are visited twice a week by buddies, but they do not specifically monitor the nutritional

2013 Clinical Trials

262. Effects of a Resistance Training Period on Blood Pressure of Hypertensive Elderlies: Influence of the Polymorphism of the Angiotensin Converting Enzyme

training period. Before the 16 weeks ACE gene was genotyped (PCR). Before and after 16 weeks, blood pressure (ambulatory), HDL-cholesterol, Total cholesterol, Glycemia, Triacylglycerol (colorimetric assay) and plasminogen activator inhibition (PAI-1), intercellular adhesion molecule (ICAM-1), vascular endothelial cell adhesion molecule (VCAM-1), Adiponectin, tumor necrosis factor alpha (TNF-alpha), C Reactive Protein, Angiotensin II, Angiotensin Converting Enzyme, Angiotensin 1-7, (ELISA assay) were (...) 2013 Actual Study Completion Date : April 2013 Resource links provided by the National Library of Medicine related topics: Arms and Interventions Go to Arm Intervention/treatment Experimental: Resistance training Resistance training performed three times at week for 16 weeks, in 8 exercises for the main muscles, the protocol of 3 sets of 10 repetitions with intensity of 50% of 1 maximum repetition (MR). Behavioral: Resistance training Resistance training performed three times at week for 16 weeks

2013 Clinical Trials

263. Nighttime Macronutrient Choice and Combined Resistance and High-intensity Interval Training

in Overweight and Obese Adults Study Start Date : September 2011 Actual Primary Completion Date : August 2012 Actual Study Completion Date : November 2012 Resource links provided by the National Library of Medicine available for: Arms and Interventions Go to Arm Intervention/treatment Experimental: Whey Protein and Exercise Training This arm involves 4 weeks of consuming a whey protein supplement late in the evening before bed along with combined resistance and high-intensity interval training 3 days per (...) lift 1-time through a full range of motion and all attempts and will be supervised by trained personnel Eligibility Criteria Go to Information from the National Library of Medicine Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Layout table

2013 Clinical Trials

264. Motivational Support and Meal Preparation Training to Reduce Vascular Risk After Gestational Diabetes

activity levels. However, many women find it difficult to alter their lifestyle habits, especially if they have young children. In adults with type 2 diabetes, the investigators have been studying the effects of combining nutrition education with meal preparation training and pedometer-based self-monitoring to improve eating habits and increase activity levels. The investigators have shown that such a strategy can reduce hemoglobin A1C by 0.3% and correlates with small reductions in weight (Dasgupta et (...) Motivational Support and Meal Preparation Training to Reduce Vascular Risk After Gestational Diabetes Motivational Support and Meal Preparation Training to Reduce Vascular Risk After Gestational Diabetes - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please

2013 Clinical Trials

265. Effects of Moderate Altitude Training on Metabolic Parameters in Voluntary Study Participants With Metabolic Syndrome

well be documented and compared(fasting plasma glucose, triglycerides, HDL-C, LDL-C, insulin, C-peptid, free fatty acids, adiponectin, leptin, HbA1c, Metabolon cluster, c reactive protein, vit D3). Also BMI, BIA bioimpedance analysis, blood pressure, heart rate, egg, Physical status, exercise test. Study Design Go to Layout table for study information Study Type : Interventional (Clinical Trial) Estimated Enrollment : 40 participants Allocation: Randomized Intervention Model: Single Group (...) Assignment Masking: Single (Investigator) Primary Purpose: Prevention Official Title: Randomized Controlled Trial to Analyze the Effects of Moderate Altitude Training on Metabolic Parameters in Voluntary Study Participants With Metabolic Syndrome. Study Start Date : November 2013 Actual Primary Completion Date : November 2013 Estimated Study Completion Date : December 2014 Resource links provided by the National Library of Medicine related topics: Arms and Interventions Go to Arm Intervention/treatment

2013 Clinical Trials

266. Aerobic Training and Non-Exercise Physical Activity

Type : Interventional (Clinical Trial) Actual Enrollment : 45 participants Allocation: Randomized Intervention Model: Parallel Assignment Masking: None (Open Label) Primary Purpose: Treatment Official Title: The Intervention Composed of Aerobic Training and Non-Exercise Physical Activity (I-CAN) Study Start Date : February 2014 Actual Primary Completion Date : June 2017 Actual Study Completion Date : June 2017 Resource links provided by the National Library of Medicine related topics: Arms (...) Aerobic Training and Non-Exercise Physical Activity Aerobic Training and Non-Exercise Physical Activity - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one or more studies before adding more. Aerobic Training and Non-Exercise Physical Activity (I

2013 Clinical Trials

267. Aerobic Plus Resistance Training and Insulin Sensitivity in African American Men

Aerobic Plus Resistance Training and Insulin Sensitivity in African American Men Aerobic Plus Resistance Training and Insulin Sensitivity in African American Men - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one or more studies before adding (...) more. Aerobic Plus Resistance Training and Insulin Sensitivity in African American Men (ARTIIS) The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our for details. ClinicalTrials.gov Identifier: NCT01787617 Recruitment Status : Unknown Verified May 2016 by Robert Newton, Pennington Biomedical Research Center. Recruitment status was: Active

2013 Clinical Trials

268. Chronic Effects of Two Aerobic-training Models Performed in Water and on Dry Land in Patients With Type 2 Diabetes Mellitus (T2DM).

Primary Completion Date : December 2012 Resource links provided by the National Library of Medicine related topics: Arms and Interventions Go to Arm Intervention/treatment Experimental: Aquatic exercise The aquatic aerobic training had a duration of 12 weeks and adopted the interval-training method, with intensities ranging between 85 and 100% of second ventilatory threshold (VT2) and total duration of 45 minute per session. The sessions consisted of warm up, main part and calm down. The warm-up (...) failure (GFR by MDRD <30). Muscle or joint injury that prevents physical exercises. Contacts and Locations Go to Information from the National Library of Medicine To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor. Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01956357 Locations Layout table for location information Brazil Physical Education School of Federal University of Rio

2013 Clinical Trials

269. Physical Fitness Training in Subacute Stroke (PHYS-Stroke)

, 2017 Resource links provided by the National Library of Medicine related topics: Arms and Interventions Go to Arm Intervention/treatment Experimental: physical fitness training aerobic physical fitness training Procedure: physical fitness training Active Comparator: relaxation non-aerobic training Procedure: relaxation Outcome Measures Go to Primary Outcome Measures : Gait speed and Barthel Index (BI) (co-primary endpoint) [ Time Frame: 3 months post stroke vs baseline ] comparing gait speed (m/s (...) insulin, glucose, and HbA1c in aerobic and non-aroebic training group after the 4-week intervention interval as well as after 3 and after 6 months post stroke vs baseline (before intervention) lipid profile [ Time Frame: directly after intervention; 3 months post stroke; 6 months post stroke; all vs baseline ] comparing lipide such as triglycerides, cholesterol (total, LDL,HDL, and LP(a)) in aerobic and non-aroebic training group after the 4-week intervention interval as well as after 3 and after 6

2013 Clinical Trials

270. Resistance Training as an Aid to Smoking Cessation Treatment

: Randomized Intervention Model: Single Group Assignment Masking: None (Open Label) Primary Purpose: Treatment Official Title: Resistance Training as an Aid to Smoking Cessation Treatment Study Start Date : November 2013 Estimated Primary Completion Date : March 2019 Estimated Study Completion Date : March 2019 Resource links provided by the National Library of Medicine related topics: Arms and Interventions Go to Arm Intervention/treatment Experimental: Resistance training Participants will attend two, 45 (...) Resistance Training as an Aid to Smoking Cessation Treatment Resistance Training as an Aid to Smoking Cessation Treatment - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one or more studies before adding more. Resistance Training as an Aid

2013 Clinical Trials

271. Cognition and Exercise Training

: 160 participants Allocation: Randomized Intervention Model: Parallel Assignment Masking: None (Open Label) Primary Purpose: Prevention Official Title: Cerebral Oxygenation, Cardiac Output,Cognitive Function, and Exercise Training in Patients With Metabolic Syndrome, Coronary Heart Disease and Chronic Heart Failure. Actual Study Start Date : September 2013 Actual Primary Completion Date : September 2018 Estimated Study Completion Date : October 2019 Resource links provided by the National Library (...) Cognition and Exercise Training Cognition and Exercise Training - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one or more studies before adding more. Cognition and Exercise Training (COGNEX-2) The safety and scientific validity of this study

2013 Clinical Trials

272. High Intensity Interval Versus Continuous Moderate Intensity Training: Maximizing the Benefits of Exercise in Overweight Adolescents

: Interventional (Clinical Trial) Actual Enrollment : 30 participants Allocation: Randomized Intervention Model: Parallel Assignment Masking: Single (Outcomes Assessor) Primary Purpose: Prevention Official Title: High Intensity Interval Versus Continuous Moderate Intensity Training: Maximizing the Benefits of Exercise in Overweight Adolescents. Study Start Date : February 2013 Actual Primary Completion Date : October 2014 Actual Study Completion Date : December 2014 Resource links provided by the National (...) /wk for 6wks. Other: Moderate Intensity Training Outcome Measures Go to Primary Outcome Measures : Body Composition as measured by DXA [ Time Frame: Baseline and 6 weeks ] Secondary Outcome Measures : Body Weight [ Time Frame: Baseline and 6 weeks ] Blood Pressure [ Time Frame: Baseline and 6 weeks ] Body Mass Index [ Time Frame: Baseline and 6 weeks ] Peak uptake of volume of oxygen [ Time Frame: Baseline and 6 weeks ] Wingate Cycle test [ Time Frame: Baseline and 6 weeks ] LDL Cholesterol [ Time

2013 Clinical Trials

273. Effect of a High-Protein Diet and/or High-Intensity Training on Metabolic Syndrome

diet interventions have been shown to be effective in reducing triglycerides and increasing high-density lipoprotein cholesterol concentrations. Low-volume, high-intensity cycling exercise has shown to elicit positive effects on metabolic syndrome risk factors such as triglyceride concentrations. The objective of this study was to determine the combined effects of a high-protein, reduced carbohydrate diet and high-intensity interval training on metabolic syndrome risk factors in women. The second (...) Training: A Diabetes Prevention Program for Women Study Start Date : February 2012 Actual Primary Completion Date : March 2013 Actual Study Completion Date : March 2013 Resource links provided by the National Library of Medicine related topics: Arms and Interventions Go to Arm Intervention/treatment Active Comparator: Higher Protein Diet (PRO) Other: Higher PRO Diet Participants in the PRO and PRO+EX groups will meet weekly with a diet specialist on staff to monitor their intake and compliance

2012 Clinical Trials

274. Xbox Kinect Training in Men With Prostate Cancer

information Study Type : Interventional (Clinical Trial) Actual Enrollment : 46 participants Allocation: Randomized Intervention Model: Parallel Assignment Masking: Double (Investigator, Outcomes Assessor) Primary Purpose: Treatment Official Title: Xbox Kinect Training in Men With Metastatic Prostate Cancer Receiving Androgen Deprivation Therapy Actual Study Start Date : February 2015 Actual Primary Completion Date : June 2018 Actual Study Completion Date : June 2018 Resource links provided (...) Frame: Change from baseline to week 12 and week 24 ] Plasma cholesterol (mmol/L) The effect of 12 weeks systematically training with the Xbox Kinect system on metabolic parameters [ Time Frame: Change from baseline to week 12 and week 24 ] Plasma High-density lipoprotein (HDL-cholesterol) (mmol/L) The effect of 12 weeks systematically training with the Xbox Kinect system on metabolic parameters [ Time Frame: Change from baseline to week 12 and week 24 ] Plasma Low-density lipoprotein (LDL

2012 Clinical Trials

275. Nutrition Education Intervention in Adults With Type 2 Diabetes Mellitus in a Resource Poor Setting

Nutrition Education Intervention in Adults With Type 2 Diabetes Mellitus in a Resource Poor Setting Nutrition Education Intervention in Adults With Type 2 Diabetes Mellitus in a Resource Poor Setting - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please (...) remove one or more studies before adding more. Nutrition Education Intervention in Adults With Type 2 Diabetes Mellitus in a Resource Poor Setting The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our for details. ClinicalTrials.gov Identifier: NCT01095965 Recruitment Status : Completed First Posted : March 30, 2010 Last Update Posted : January 12, 2015

2010 Clinical Trials

276. Sotagliflozin with insulin for treating type 1 diabetes

that is evidence based, quality assured, delivered by trained educators and includes information about diabetic ketoacidosis, such as: how to recognise its risk factors, signs and symptoms how and when to monitor blood ketone levels what actions to take for elevated blood ketones and treatment is started and supervised by a consultant physician specialising in endocrinology and diabetes treatment, and haemoglobin A1c (HbA1c) levels are assessed after 6 months and regularly after this. 1.2 Stop sotagliflozin (...) of treatment outweighs the risk of diabetic ketoacidosis and this would require specialist knowledge. Low insulin need is defined as less than 0.5 units of insulin/kg of body weight/day in NICE's technology appraisal guidance on dapagliflozin with insulin for type 1 diabetes. In the same guidance, the clinical population consisted of people: with a BMI of 27 kg/m 2 or more who have completed a structured education programme with insulin needs of 0.5 units/kg of body weight/day or more with inadequate

2020 National Institute for Health and Clinical Excellence - Technology Appraisals

277. Hypertension in adults: diagnosis and management

. However, the committee noted that implementation of the 2011 recommendations on ABPM has been challenging and that there is still variation in practice. A change in practice and additional resources and training will be needed in areas where there is currently no access to ABPM devices. However, ABPM was found to be the most cost-effective method of diagnosis, and it is anticipated that the long-term benefits of accurate diagnosis and treatment (such as avoiding over diagnosis and unnecessary (...) pressure targets 28 Step 1 treatment 31 Step 2 and 3 treatment 33 Step 4 treatment 34 Identifying who to refer for same-day specialist review 35 Context 38 Finding more information and resources 39 Update information 40 Hypertension in adults: diagnosis and management (NG136) © NICE 2019. All rights reserved. Subject to Notice of rights (https://www.nice.org.uk/terms-and- conditions#notice-of-rights). Page 3 of 40This guideline replaces CG127. This guideline partially replaces NG28. This guideline

2019 National Institute for Health and Clinical Excellence - Clinical Guidelines

278. Stroke and transient ischaemic attack in over 16s: diagnosis and initial management

or acute non-disabling stroke 24 Thrombectomy for people with acute ischaemic stroke 25 Blood pressure control for people with acute intracerebral haemorrhage 28 Optimal positioning for people with acute stroke 30 Early mobilisation for people with acute stroke 30 Decompressive hemicraniectomy for people with acute stroke 31 Context 34 Finding more information and resources 36 Update information 37 Stroke and transient ischaemic attack in over 16s: diagnosis and initial management (NG128) © NICE 2019 (...) and referred urgently for carotid endarterectomy to a service following current national standards [1] receive best medical treatment (control of blood pressure, antiplatelet agents, cholesterol lowering through diet and drugs, lifestyle advice). [2008, amended 2019] [2008, amended 2019] 1.2.5 Ensure that people with stable neurological symptoms from acute non-disabling stroke or TIA who have symptomatic carotid stenosis of less than 50% according to the NASCET criteria, or less than 70% according

2019 National Institute for Health and Clinical Excellence - Clinical Guidelines

279. Effects of Niacin on Good Cholesterol in People With Peripheral Arterial Disease

Effects of Niacin on Good Cholesterol in People With Peripheral Arterial Disease Effects of Niacin on Good Cholesterol in People With Peripheral Arterial Disease - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one or more studies before adding (...) more. Effects of Niacin on Good Cholesterol in People With Peripheral Arterial Disease The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our for details. ClinicalTrials.gov Identifier: NCT01391377 Recruitment Status : Terminated (Tredaptive has been suspended worldwide) First Posted : July 12, 2011 Last Update Posted : February 27, 2013 Sponsor

2011 Clinical Trials

280. A Safety and Efficacy Study of DRL-17822, a Cholesteryl Ester Transfer Protein (CETP) Inhibitor, in Patients With Abnormal Cholesterol Levels

A Safety and Efficacy Study of DRL-17822, a Cholesteryl Ester Transfer Protein (CETP) Inhibitor, in Patients With Abnormal Cholesterol Levels A Safety and Efficacy Study of DRL-17822, a Cholesteryl Ester Transfer Protein (CETP) Inhibitor, in Patients With Abnormal Cholesterol Levels - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save (...) this study Warning You have reached the maximum number of saved studies (100). Please remove one or more studies before adding more. A Safety and Efficacy Study of DRL-17822, a Cholesteryl Ester Transfer Protein (CETP) Inhibitor, in Patients With Abnormal Cholesterol Levels The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our for details

2011 Clinical Trials

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