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NCT ID: NCT02769052 Completed - Endometriosis Clinical Trials

TENS Self-applied in the Complementary Treatment of Deep Endometriosis

tici_mira
Start date: June 2016
Phase: N/A
Study type: Interventional

Objective: to evaluate the effectiveness of Transcutaneous Electrical Nerve Stimulation (TENS) self-applied for the treatment of pain and the impact of this therapy on quality of life and sexuality of women with deep endometriosis.

NCT ID: NCT02768480 Completed - Diabetes Mellitus Clinical Trials

Effectiveness of Phone Calls Intervention on Diabetic Patients After Ambulatory Discharge of a Tertiary Care Center

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

The study is a randomized clinical trial, controlled, open label that aimed to compare two groups after discharge of a tertiary care: type 2 diabetes patients followed exclusively by primary care (control group) and patients followed by primary care and supported by phone calls (intervention group).

NCT ID: NCT02767804 Active, not recruiting - Clinical trials for Non-small Cell Lung Cancer

eXalt3: Study Comparing X-396 (Ensartinib) to Crizotinib in ALK Positive Non-Small Cell Lung Cancer (NSCLC) Patients

Start date: June 2016
Phase: Phase 3
Study type: Interventional

The primary purpose of this study is to evaluate the efficacy and safety of X-396 (ensartinib) vs. crizotinib in patients with ALK-positive non-small cell lung cancer that have received up to 1 prior chemotherapy regimen and no prior ALK inhibitor.

NCT ID: NCT02767258 Recruiting - Dry Eye Syndromes Clinical Trials

Effect of Nursing Care on Prevention of Dry Eye

Start date: May 1, 2016
Phase: N/A
Study type: Interventional

Clinical trial for prevention, randomized controlled, parallel, double-blind, with three arms, which purpose is verify the nursing interventions (artificial tear gel and liquid artificial tears)effects to prevent dry eye in adult patients admitted in ICU.

NCT ID: NCT02766361 Active, not recruiting - Bipolar Disorder Clinical Trials

Cognitive-Behavioral Rehabilitation for Bipolar Disorder

REHABBipolar
Start date: March 2016
Phase: Phase 1/Phase 2
Study type: Interventional

The study consists of a clinical trial comparing a new structured group intervention, denominated "Cognitive-Behavioral Rehabilitation", to treatment as usual (TAU) for bipolar patients. The new approach is a combination of cognitive behavioral strategies and cognitive rehabilitation exercises, consisting of twelve weekly group sessions of 90 minutes each. To be included in the study, patients must be diagnosed with bipolar disorder, type I or II, be 18 to 55 years old, in full or partial remission and have an IQ of at least 80. A comprehensive neuropsychological battery, followed by mood, social functioning and quality of life assessments will occur in three moments: pre and post-intervention and after 12 months.

NCT ID: NCT02766036 Completed - Clinical trials for Chronic Kidney Diseases

Propolis Effects in Patients With Chronic Kidney Disease

Start date: December 1, 2016
Phase: Phase 2
Study type: Interventional

The aim of this study is to determine the impact of Propolis on proteinuria reduction and protection of the glomerular filtration rate in chronic renal failure patients.

NCT ID: NCT02765321 Recruiting - Health Behavior Clinical Trials

Populational Program of Physical Activity and Healthy Eating Promotion: the "Life of Health" Study

Life of Health
Start date: April 2016
Phase: N/A
Study type: Interventional

This is a population-based "natural experiment" study aimed to examine the effect of a multi-approach intervention focused on physical activity and healthy eating promotion to individuals living in Jaguariuna city (São Paulo, Brazil).

NCT ID: NCT02765152 Recruiting - Stroke Clinical Trials

Effects of Training Rhythmic and Discrete Aiming Movements on Arm Control and Functionality After Stroke

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

The purpose of this study is to verify the additional effects of rhythmic specific training, discrete specific training additional to conventional therapy on the upper limb after chronic stroke subjects on the outcomes: motor control and functionality.

NCT ID: NCT02764840 Completed - Clinical trials for Muscle Strength Quantitative Trait Locus 1

Muscular Resistance Test in the Elastic Tube: Reliability and Training of the Proposed Method

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

Resistance exercises from elastic tube has been used as part of the rehabilitation and maintenance of muscle tone levels in different scenarios, from disease conditions to the sports universe. There is the convenience and low cost of the instrument, which can provide impact on clinical and economic framework in case of spillage of use strategies. In a recent search, the investigators were not observed data on the reliability and reproducibility of a specific test for this tool and in this sense, it seems pertinent to undertake research on the topic. Objectives: To determine the reliability and reproducibility by comparison with a isokinetic muscle strength test located â fatigue held in elastic tube and compare the results of a training protocol for muscle strength gain in both methods, elastic tube and dynamometer. Methods: Participants will perform the muscular endurance test localized fatigue, on two occasions, with an interval of seven days between them. Everyone will accomplish so much in the elastic tube, as in the isokinetic dynamometer. It will be held evaluator analysis intra and inter evaluator. After first stage of the study to determine the reliability test, the participants will undergo three weeks of training to gain muscular endurance, distributed in two groups G1 (training in the elastic tube) and G2 (training in isokinetic dynamometer) previously randomized. It will use the intra-class correlation coefficient with 95% confidence interval to check the repeatability and the Kappa coefficient with 95% confidence interval for reproducibility. To compare the responses of training, the distribution will be made as to the normality of the data by the Kolmogorov-Smirnov test. In the case of normal distribution, the Student's t-test for unpaired data and Mann-Whitney will be adopted if there is no normal distribution.

NCT ID: NCT02764047 Recruiting - Clinical trials for Non-alcoholic Fatty Liver Disease

Probiotics in the Treatment of NAFLD

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

Evaluate the effect of supplementation of probiotics on liver changes (histological and enzymatic), lipid profile and gut microbiota of patients with nonalcoholic steatohepatitis (NASH).