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Blood Glucose clinical trials

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NCT ID: NCT04578067 Recruiting - Physical Activity Clinical Trials

Empowering Immigrant Women for Active and Healthy Lifestyle

Start date: September 30, 2020
Phase: N/A
Study type: Interventional

The study will include overweight and obese otherwise healthy women, recruited from two main borough in Oslo with the highest population of Somali origin. The study comprises two phases: A 12-months controlled trial where the participants in the intervention borough will be compared to participants in the control borough. This is followed by a 12-months maintaining phase for the intervention borough where the control group will be given the same intervention as the intervention group received during the first 12-months.

NCT ID: NCT04451655 Completed - Blood Glucose Clinical Trials

Glycemic Stability During the Intraoperative Period Among Patients With DM Undergoing CABG Surgery

Start date: September 1, 2018
Phase: N/A
Study type: Interventional

Objectives: Intraoperative glycemic stability and control among patients with diabetes mellitus (DM) undergoing coronary artery bypass grafting (CABG) surgery remains a significant concern. In this study, the intraoperative glycemic stability among diabetic patients undergoing CABG surgery was compared between patients who received an intravenous continuous insulin infusion (CII) for tight glycemic control with those who received an CII for conventional glycemic control, during the intraoperative period. Research Design and Methods: This study implemented a quasi-experimental design with a convenience sample of 144 patients with DM undergoing CABG surgery at a major hospital in Amman, Jordan.

NCT ID: NCT04424238 Active, not recruiting - Diet Habit Clinical Trials

the Effect of Mobile Medical Used for the Standardized Management of Gestational Diabetes

Start date: March 15, 2016
Phase: N/A
Study type: Interventional

A multicenter, randomized controlled trial was conducted to investigate whether health education and life style management through WeChat group chat was more effective in controlling blood glucose (BG) than standard clinic prenatal care in women with GDM.

NCT ID: NCT04396262 Completed - Blood Glucose Clinical Trials

Effect of Processed Blueberry on Blood Glucose and Antioxidant Status in Human Adults

Start date: November 1, 2015
Phase: N/A
Study type: Interventional

Canada's Food Guide (2007) recommended 7-10 servings of fruits and vegetables per day for a normal adult population. Although fruit juice (125 ml) is considered as one serving of fruits, the consumption of some fruit juices may be limited due to their high amount of sugar. The consumption of sugary drinks can lead to a rapid rise in postprandial glycaemia. Wild blueberries, due to their high level of anthocyanins, may provide multiple health benefits including improved blood glucose control, however, the consumption of fresh berries is limited by their short seasonal availability. Hydro-Thermodynamic (HTD) processing of blueberries allows the processing of whole berries including their skin and seeds into a beverage with the amount of anthocyanins comparable with fresh berries. The objective of the study is to investigate the effect of HTD-processed blueberries on postprandial glycaemia and antioxidant activity.

NCT ID: NCT04378374 Completed - Blood Glucose Clinical Trials

The Effect of Pulse Flours on Blood Glucose, Satiety and Food Intake

Start date: September 16, 2019
Phase: N/A
Study type: Interventional

Pulse flours represent a fast-growing segment on the functional food market; however, their health effects are not well understood. The observational studies and acute trials have established the link between frequent consumption of cooked whole pulses (beans, peas, lentils and chickpeas) and healthier body weight and improved blood glucose control. However, it is not clear whether these effects still remain after the processing of pulses into flours. The investigators hypothesized that the baked food products formulated with lentil flour of the same particle size as all-purpose wheat flour may reduce postprandial glycaemia and elicit a stronger suppression of subjective appetite due to its higher content of protein and resistant carbohydrate compared to all-purpose wheat flour. The treatments will be formulated either with lentil flour or with all-purpose wheat flour of similar particle size or with their combination. The objective of the project is to test the effect of foods formulated with lentil flour and/or wheat flour on blood glucose, short-term food intake and subjective appetite.

NCT ID: NCT04260425 Completed - Blood Glucose Clinical Trials

A Pilot Study Evaluating Oat Polyphenols on Post-prandial Glucose Response

Start date: November 28, 2021
Phase: N/A
Study type: Interventional

The trial will use a two period acute double-blind cross-over design to compare the effects of a serving of oatmeal containing high or low amounts of avenanthramides (AV) on post-prandial blood glucose response in healthy adults.

NCT ID: NCT04258501 Completed - Blood Glucose Clinical Trials

Exploratory Study of Efficacy on Selected Natural Extracts Reducing Post Prandial Blood Glucose Response

Start date: November 24, 2011
Phase: N/A
Study type: Interventional

Randomized, balanced, incomplete block design exploratory study of efficacy, with 8 active treatments (4 treatments per subject; 35 or 37 subjects per treatment) compared to a reference treatment (all 72 subjects).

NCT ID: NCT04256746 Completed - Blood Glucose Clinical Trials

Dose Response Study of a Natural Extract for Reducing Post Prandial Blood Glucose

Start date: September 24, 2012
Phase: N/A
Study type: Interventional

Randomized, balanced incomplete block design dose response study of efficacy, with 4 different dosages of mulberry fruit powdered extract added to cooked rice compared to a reference treatment (cooked rice only).

NCT ID: NCT04077203 Completed - Blood Glucose Clinical Trials

Biofeedback of Glucose in Non-diabetic Participants

Start date: July 16, 2019
Phase: N/A
Study type: Interventional

This research examines whether biofeedback of glucose (i.e., knowledge of one's own glucose levels) in non-diabetic participants affects their health behaviours (e.g., eating, nutrition, exercise, etc.). This study utilizes wearable continuous glucose (CGM) technology, which provides personalized feedback to participants to allow them to self-monitor their own glucose levels.

NCT ID: NCT03985917 Completed - Depression Clinical Trials

Singing Groups for Seniors: Well-Being, Cognitive Function and Health

Sing4Health
Start date: December 5, 2018
Phase: N/A
Study type: Interventional

The researchers' implement and measure the effects of a singing group intervention program for older adults, with an RCT design, in a natural context, on the health, well-being and cognitive function of older adults.