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Physical Activity clinical trials

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NCT ID: NCT03563027 Completed - Physical Activity Clinical Trials

Social and Financial Incentives to Increase Physical Activity Among Overweight and Obese Veterans

Start date: March 19, 2019
Phase: N/A
Study type: Interventional

In this randomized, controlled trial the investigators will compare the use of social and financial incentive-based interventions to increase physical activity among overweight and obese Veterans during a 12-week intervention with 8 weeks of follow-up.

NCT ID: NCT03551366 Completed - Physical Activity Clinical Trials

Influence of Different Physical Education Pedagogical Approaches on the Health and Development of 5-6 Year Old Children

SAMPLE-PE
Start date: January 4, 2018
Phase: N/A
Study type: Interventional

The Skill Acquisition Methods underpinning Pedagogy for LEarning in Physical Education (SAMPLE-PE) project aims to investigate the influence of different pedagogical approaches to teaching and learning in physical education (PE) on 5-6 year old children's health and development. Schools from deprived areas are invited to take part in the project and will be randomly assigned to either: (1) linear pedagogy PE curriculum programme, (2) nonlinear pedagogy PE curriculum programme or (3) carry on as normal. The linear and nonlinear pedagogy PE programmes will be underpinned by different and contrasting theories of skill acquisition and are delivered by trained coaches over 15 weeks. Children will be measured to assess their physical, psychological, cognitive, and emotional health and development, and their physical activity levels at the start of the study, immediately after the 15 week PE programme, and again after 12 months. It is expected that children taking part in the linear and nonlinear PE programmes will demonstrate greater physical development than children attending schools that carry on as normal. Furthermore, it is also anticipated that children taking part in the nonlinear PE programme will show greater gains in psychological, cognitive and emotional outcomes than the linear and usual practice programmes.

NCT ID: NCT03550105 Completed - Diabetes Mellitus Clinical Trials

Effects of Simulated Passive Jogging Device on Glucose Homeostasis, Muscle Strength and Endurance

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

Physical Inactivity and excessive sedentary behavior are risk factors for diabetes and cardiovascular disease. Movement is important for overall health. This study will assess the validity and usefulness of low risk, non-invasive wellness device, the Gentle Jogger® (GJ) that passively simulates the physical activities of jogging. The study will evaluate whether or not use of GJ modifies glycemic control and muscle strength in subjects who are known to be diabetic and those who are not. The study volunteers are subjects between the ages of 25-80yr.

NCT ID: NCT03548350 Completed - Physical Activity Clinical Trials

School Based Physical Activity Interventions and Its Impact on Wellbeing and Educational Outcomes

Start date: September 2016
Phase: Phase 1
Study type: Interventional

A school based Physical Activity intervention for pupils (8-9 years old) to promote fitness and wellbeing

NCT ID: NCT03545152 Completed - Clinical trials for Mild Cognitive Impairment

Non-pharmacological Interventions on Cognitive Functions in Older People With Mild Cognitive Impairment

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

This project is proposed to be a three-year project. The purposes of this project are to develop and examine physical activity program, cognitive rehabilitation training, and new life-style (combination of exercise and cognitive) interventions on primary outcomes (cognitive function), and secondary outcomes (physical fitness, QOL and depression) among community-dwelling elderly adults with MCI.

NCT ID: NCT03544489 Completed - Physical Activity Clinical Trials

Implementing Exercise After an (ICD)

E-ICD
Start date: July 1, 2019
Phase: N/A
Study type: Interventional

This is the first feasibility test of a highly portable home-based exercise intervention after an ICD, using technology monitoring (rather than self-report) of intervention progress and outcomes. Evidence for intervention effectiveness will inform algorithms for initiating exercise post-ICD more broadly in clinical practice. This study aligns directly with recent scientific statements that recommend testing behavioral interventions for ICD patients that are based on participant engagement, use cognitive behavioral approaches, and are readily available when most needed.

NCT ID: NCT03543332 Completed - Physical Activity Clinical Trials

Physical Activity After Cardiac Arrest; a Sub-study in the Target Temperature Management Trial 2

Start date: July 21, 2018
Phase:
Study type: Observational

The Target Temperature Management trial 2 (TTM2) is an international multi-center study, that randomize patients with OHCA of a presumed cardiac or unknown cause to target temperature management at 33°C or normothermia but avoiding fever (37.8°C) for the first 24 hours after the OHCA. The TTM2 study (clinicaltrials.gov Identifier NCT02908308) includes a detailed follow-up of functional outcome, health-related quality of life and neurocognitive function at 6 and 24 months post-arrest. This protocol describes a sub-study within the TTM2 trial that specifically focus on physical activity among the OHCA survivors.

NCT ID: NCT03539237 Completed - Physical Activity Clinical Trials

Closing the Gap Between Self-reported and Accelerometer-based Physical Activity

GAP
Start date: May 23, 2018
Phase: N/A
Study type: Interventional

This study examines the effect of a video-based intensity level demonstration on self-reported physical activity in individuals aged between 40 and 75 years. Aim of the video demonstration is to achieve a better concordance of physical activity reports with accelerometer-based measurements.

NCT ID: NCT03538834 Completed - Healthy Clinical Trials

The Effects of Dietary Intake of Cod Residual Material Meal on Lipid Regulation, Glucose Regulation and Body Composition in Physically Active Adults

COD2016
Start date: January 2016
Phase: N/A
Study type: Interventional

A high intake of fish is associated with positive health effects, including prevention and treatment of chronic non-communicable diseases, such as cardiovascular diseases (CVDs) and type 2 diabetes. These health effects have traditionally been attributed to the omega-3 fatty acids in fatty fish, but recent studies have suggested that also fish proteins may improve biomarkers of metabolic disease. Intake of cod fillet have previously shown beneficial effects on blood lipids, glucose regulation and body composition in adults with overweight or obesity. Health effect of cod residual material from fillet production (i.e., head, backbone, skin, cutoffs and entrails) have so far not been investigated, but residuals from other fish species have shown promising effects on glucose regulation in rats. The main aim of the current study is to investigate the effects of cod residual meal on serum lipids and glucose regulation in healthy, physically active adults.

NCT ID: NCT03538158 Completed - Aging Clinical Trials

A Personalized Health Behavior System

FITTLESenior
Start date: November 26, 2018
Phase: N/A
Study type: Interventional

The objectives of this study are to examine the usability and efficacy, for diverse older adults, of a new tablet-based dynamic system: the Fittle Senior System (FSS) that will provide: (1) personalized behavior-change programs for improved diet and increased physical activity and (2) online social interaction and support from small teams pursuing similar goals. The proposed study involves a two group randomized trial where participants will be randomized to the Fittle Senior System or to a paper-based psycho-educational control condition following a baseline assessment. The duration of the intervention phase will involve an active 12-week intervention phase followed by a 12-week maintenance phase. We will recruit and randomize 180 community dwelling adults aged 65+ years, who live alone and are at risk for social isolation. Participants will be assessed at baseline, 3 months post active intervention and 3 months post maintenance (6 months following active intervention) on measures of health and health behaviors, and indices of social support.