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Physical Activity clinical trials

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NCT ID: NCT03253406 Completed - Physical Activity Clinical Trials

Health Wearables and College Student Health

Start date: September 6, 2017
Phase: N/A
Study type: Interventional

The purpose of this pilot randomized trial is to determine (1) the effectiveness of the Polar M400, used in combination with a twice-weekly Facebook-delivered Social Cognitive Theory-based health intervention, in the promotion of more healthful physical activity and nutritious eating behaviors over 12 weeks in college students versus a comparison group; and (2) the validity and reliability of the Polar M400 in the assessment of free-living (i.e., non-laboratory based) physical activity (in this case, steps per day and daily durations of moderate and vigorous physical activity) and energy expenditure.

NCT ID: NCT03250000 Recruiting - Physical Activity Clinical Trials

Changes in Microcirculation and Functional Status During Exacerbation of COPD

COPD-EX
Start date: September 8, 2017
Phase: N/A
Study type: Observational

This study investigates the influence of acute exacerbation of chronic obstructive pulmonary disease (COPD) on retinal microcirculation, on functional status and also investigates the prognostic value of retinal vessel caliber assessment in terms of hospitalization and mortality during 2 years of follow-up.

NCT ID: NCT03248752 Completed - Physical Activity Clinical Trials

Monitoring Physical Activity (Fitbit)

Start date: July 4, 2017
Phase: N/A
Study type: Interventional

The purpose of this study is to examine the effect of monitoring and sharing physical activity outcomes (using Fitbit technology) with a domestic partner on physical activity participation. Primary research question: Does sharing physical activity outcomes from wearable technology with a participant's partner improve overall physical activity over 3 months compared to not sharing outcomes? Physical activity will be measured as minutes of moderate to vigorous physical activity per week. Hypothesis: Knowledge that physical activity outcomes are visible to a participant's partner will serve as a proxy-supervision intervention. Awareness of partner's progress will serve as further motivation. Both factors will improve physical activity adherence in comparison to participants without shared outcomes.

NCT ID: NCT03247426 Completed - Physical Activity Clinical Trials

Sleep Quality, Job Satisfaction, Quality of Life, Occupational Burnout Levels in Individuals

Start date: August 15, 2017
Phase: N/A
Study type: Observational

The aim of this study is to compare sleep quality, job satisfaction, quality of life, occupational burnout levels among individuals who do or do not do exercise.

NCT ID: NCT03245164 Completed - Physical Activity Clinical Trials

The Effects of Group Exercise and Basketball on Obese Children

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

This study aimed to compare the effects of group exercises under physiotherapist control and basketball program on body composition and motor skills of obese children. 45 obese children aged 10 years were randomly included to the physiotherapy (n=15), basketball (n:15), and control group (n:15). The children were assessed before and after 12-week study duration. Body Mass Index (BMI), the percentage of body fat, and circumference values of the children were recorded. Bruininks-Oseretsky Test of Motor Proficiency-Brief Form (BOTMP-BF) was used to determine motor skills of children.

NCT ID: NCT03244150 Completed - Obesity Clinical Trials

Youth and Sport Study

YSS
Start date: August 1, 1983
Phase: N/A
Study type: Observational

The Youth and Sport Study (YSS) is a 20-22-year follow-up study of Danish teenagers born between 1964 and 1969. Baseline data originate from two different studies carried out in 1983 and 1985, and the follow-up study was carried out in 2005.

NCT ID: NCT03241524 Completed - Physical Activity Clinical Trials

Consistency of Questionnaires to Evaluating Sexual Functions in Young Healthy Women

Start date: March 12, 2016
Phase: N/A
Study type: Interventional

The sample comprised 31 female undergraduate students attending a private University in João Pessoa, northeastern Brazil. The inclusion criteria were: age between 19 and 35 years, heterosexual, active sex life, living in a stable relationship for at least 6 months no pregnancy or parturition in the last 6 months, clinically healthy and agreeing with the terms for participating in the study. All participants gave their informed consent to take part in the study.

NCT ID: NCT03238183 Not yet recruiting - Physical Activity Clinical Trials

Effects of Dextrose on Knee Osteoarthritis

Start date: August 2017
Phase: Phase 4
Study type: Interventional

Using double blind, randomized controlled design to study the immediate, short-term and intermediate-term therapeutic effects of ultrasound guided hyaluronic acid injection and hyaluronic acid combined dextrose injection to patients with knee osteoarthritis.

NCT ID: NCT03236532 Completed - Physical Activity Clinical Trials

Effect of Supplementation With Glutamine and Exercise in Women With HIV/AIDS

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

This study aimed to investigate the effect of an exercise session with weights associated with glutamine dipeptide (GLD) supplementation on cognitive function of people living with HIV/ AIDS. The sample consisted of 10 HIV+ women, who used the Antiretroviral Therapy Highly Active. The participants were randomized in a double-blind procedure to receive seven days of supplementation GLD or placebo (PLA). At the end of this first period, the participants held a workout with weights with cognitive assessments before and immediately after the session. To evaluate oxidative stress markers blood samples were collected before and 1 hour and 2 hours after the session.Then the participants rested for 7 days for the initial stocks of glutamine return to baseline levels (washout). Following was realized the crossing of the groups, so those who had received the GLD in the first week spent extra for 7 days with PLA and vice versa, and then they repeated evaluations and exercise session. The exercise session consisted of seven resistance exercises involving different muscle groups, with three sets of 8-12 repetitions with an interval of 90 seconds between sets and 120 seconds between the exercises. Stroop test was used to cognitive assessments, which aims to assess selective attention and inhibitory control over the color of conflict and word, and the N-back test, responsible for evaluating the central executive component of working memory by stimuli visual. Oxidative stress markers (TBARS, FOX, GSH, GSSG, AOPP) were analyzed in plasma samples.

NCT ID: NCT03236363 Completed - Obesity Clinical Trials

Effectiveness of MOVI Interventions on Adiposity, Cognition and Motor Competence: MOVI-da10!

MOVI-da10!
Start date: September 19, 2017
Phase: N/A
Study type: Interventional

Project which objective is to test the effectiveness of a classroom-based physical activity intervention (MOVI-da10!) on improving, body composition, cardio-respiratory fitness and executive function.