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Physical Activity clinical trials

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NCT ID: NCT02552355 Completed - Physical Activity Clinical Trials

Milk Protein Feeding After Aerobic Exercise in Older Adults With Pre-diabetes Taking the Biguanide Metformin

Start date: August 2015
Phase: Phase 2
Study type: Interventional

The investigators propose that post-exercise milk protein feeding will enhance the mitochondrial protein synthesis (biogenesis) response to an exercise-training program. In addition, the investigators propose that this stimulatory effect of protein feeding will overcome the potential blunting effect of metformin on exercise responses. The investigators will investigate these outcomes over a 12-week exercise-training program in older adults with pre-diabetes with or without metformin treatment.

NCT ID: NCT02552134 Recruiting - Physical Activity Clinical Trials

Standardised Regional Sport-club Based Exercise Programmes

SRS
Start date: October 2016
Phase: N/A
Study type: Interventional

Background: More than 10% of the adult population in Styria, a federal state in the south of Austria, is allotted to a stationary stay at a health resort each year. In practice approximately 50.000 adults receive these stays that are financed from the health insurance companies and that last up to 3 weeks. The target group for theses stays is the general population aged between 30 and 65 years that shows minor health deficits like back pain or risk factors for cardio-metabolic diseases. The treatment during the stays consists of exercise, nutritional and psychological interventions. Thus the increase of physical activity is an important goal that is focussed during the stationary stay. Because of the absence of regional facilities that are linked to the resorts and that provide accesses to standardised regional programmes sustainability is questionable. Methods/Design: This prospective controlled open label study compares two study groups. After a stationary stay at a health resort patient are allocated to a standardised, regional sports-club based exercise programme or to another group, where only written hand-outs are provided. The primary outcome is the weekly level of health enhancing physical activity which is objectively measured with an accelerometer and an activity log-book. Additionally, social determinants are requested, fitness and anthropometric measurements are done at baseline until 12 months. Beside the changes in measurable parameters, processes are evaluated accurately. Consequently the gateway - function of the health resort is analysed. Discussion: The structured cooperation between the health sector, where health resorts informing and assigning patients to regional sports-clubs and the sports sector potentially provides a wide network of standardised programmes. Within this study we aim to evaluate the sustainability of stationary stays and a continuing regional standardised exercise programme.

NCT ID: NCT02531763 Completed - Physical Activity Clinical Trials

Behavioral Economics Framingham Incentive Trial (BE FIT)

BEFIT
Start date: September 2015
Phase: N/A
Study type: Interventional

BE FIT (Behavioral Economics Framingham Incentive Trial) is a pilot study to test the deployment of a social incentive intervention using the Framingham Heart Study (FHS) Offspring, Generation 3, and Omni cohorts to increase physical activity (PA). The investigators will leverage the strength of FHS by recruiting trios and nuclear families to test whether social connectedness increases PA. The investigators will utilize a randomized controlled trial design. The investigators will test a social incentive intervention strategy using a team-based design in which participants work together to jointly achieve their PA goals, and a social connectedness intervention.

NCT ID: NCT02531022 Completed - Physical Activity Clinical Trials

Evaluating Increasing Physical Activity After Acute Coronary Syndrome

Start date: February 2016
Phase: N/A
Study type: Interventional

This study will use a randomized, controlled trial to test the effectiveness of a home-based physical activity program using wearable devices and financial incentives. All participants in will establish a baseline step count during the first two weeks and then proceed to a 16-week intervention period and 8-week follow-up period.

NCT ID: NCT02528669 Completed - Physical Activity Clinical Trials

Patient Ambulation in Post-Op Recovery

Start date: July 23, 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to create a platform that accurately measures and reports patient physical activity before a procedure, during the hospital stay, and after discharge from the hospital.

NCT ID: NCT02519946 Completed - Physical Activity Clinical Trials

On-Line Intervention to Lower Cardiovascular Risk in Pediatric Heart Transplant Patients

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

Pediatric heart transplant patients have a high-risk cardiovascular profile affecting their long-term outcomes and survival. Currently, no effective cardiovascular preventative care is provided for this pediatric population, in part, due to the fact that clinic-based programs are not easily accessible to children and their families. However, tele-health has been show to improve medical outcomes by making care more accessible to these patients. This study aims to meet the urgent need for an effective and sustainable delivery of preventative care to pediatric heart transplant patients using a diet and exercise intervention program delivered live over the internet direct to these patients' homes.

NCT ID: NCT02517762 Completed - Physical Activity Clinical Trials

Acute Low Back Pain: Causes, Mechanisms, Treatment and Followup

ALBP
Start date: March 2005
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate acute low back pain, its origin, mechanisms, the cause of pain, evaluation of treatments and development. Employees from a large local manufacturing company are sent for a complete orthopedic and pain evaluation immediately after onset of acute low back pain. Thereafter, the included patients are allocated either to the advice to stay as active as possible in spite of the pain or to adjust their activity to the pain. Pain intensity and physical activity are followed prospectively over seven days using a diary and a pedometer.

NCT ID: NCT02516345 Completed - Physical Activity Clinical Trials

Randomized Controlled Trial of an Incentive-based Physical Activity Program Targeting Both Children and Adults (FIT-FAM)

FIT-FAM
Start date: November 25, 2015
Phase: N/A
Study type: Interventional

This study aims to test whether incentives can motivate children to promote increased physical activity of a working parent while also increasing their own activity levels.

NCT ID: NCT02507869 Completed - Physical Activity Clinical Trials

A Trial of an Affect-Guided Physical Activity Prescription

Start date: April 2013
Phase: N/A
Study type: Interventional

Despite awareness of the benefits of engaging in regular physical activity, at least 50% of adults in the US do not meet recommended guidelines for physical activity. One potential explanation for this lack of regular physical activity is that people often experience exercise as affectively unpleasant. Evidence suggests that the more positively people experience exercise (i.e., the better they feel while exercising), the more likely they are to engage in regular physical activity. This may be especially true for people in poor cardiorespiratory condition. In this randomized trial, investigators compared the effects of an affect-guided exercise prescription (intervention) to a heart rate-guided exercise prescription (control) on change in physical activity minutes among previously underactive adults. Investigators also tested whether the effect of the intervention was moderated by differences in cardiorespiratory fitness.

NCT ID: NCT02496507 Completed - Physical Activity Clinical Trials

A Mixed-methods Evaluation of Sit-stand Workstations in an Office Setting

Start date: August 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate whether a device that allows office workers to sit or stand whilst working can reduce their sitting time at work and improve their health over 8 weeks.