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Range of Motion clinical trials

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NCT ID: NCT03731507 Completed - Range of Motion Clinical Trials

KinectROM Application for Assessing Range of Motion in Upper and Lower Extremity: A Development and Validation Study

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

The aim of the study is to investigate the validity and reliability of KinectROM application for objectively evaluating range of motion (ROM)

NCT ID: NCT03622645 Completed - Range of Motion Clinical Trials

An Objective Measurement Method With The Leap Motion Sensor For Hand And Wrist's Range Of Motion

Start date: January 13, 2017
Phase: N/A
Study type: Interventional

The aim of the study was to develop a low cost, clinically easy to use measurement method with the Leap motion sensor for objectively evaluating range of motion (ROM), and to investigate the validity and reliability of this application.

NCT ID: NCT03619265 Completed - Range of Motion Clinical Trials

Evaluation of Activity Levels, Inflammatory Markers, and Overall Wellness.

114-012
Start date: July 17, 2018
Phase: N/A
Study type: Interventional

The purpose for this protocol is to perform a double-blind, randomized, placebo-controlled, parallel-arm clinical study in healthy subjects to evaluate the efficacy of a nutraceutical product on physical and mental energy levels and overall wellness.

NCT ID: NCT03322956 Completed - Quality of Life Clinical Trials

Effect of Physiotherapeutic Interventions on Quality of Life in Patients With Chronic Low Back Pain. (Study 1)

CLBP
Start date: February 9, 2017
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate the effect on QoL, PI and the AROM° in patients with non-specific chronic low back pain. This after following an episode of 6 weeks 2 times a week physiotherapeutic back rehabilitation according to the 4 times T method by orthopedic disorder ® (4MTOR®). The results in this research will be analyzed and reported. In this study, 7 dependent variables will be independently examined relative to 2 independent variables.

NCT ID: NCT03309540 Recruiting - Quality of Life Clinical Trials

Effect of Physiotherapeutic Interventions on Quality of Life in Patients With Chronic Low Back Pain. (Study 2)

CLBP
Start date: October 31, 2017
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate the effect on QoL, PI and the AROM° in patients with non-specific chronic low back pain. This after following an episode of 6 weeks 2 times a week physiotherapeutic back rehabilitation according to the 4 times T method by orthopaedic disorder ® (4MTOR®). The results in this research will be analyzed and reported. In this study, 7 dependent variables will be independently examined relative to 2 independent variables.

NCT ID: NCT03194997 Completed - Breast Cancer Clinical Trials

Pilates and Dance to Breast Cancer Patients Undergoing Treatment

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

Breast cancer is one of the most common types of cancer in Brazil, and its treatment, namely surgery, chemotherapy, radiotherapy or hormone therapy, has consequences and side effects that significantly affect the quality of life and associated physical and psychological factors. The practice of physical activity, in turn, may play a beneficial role in these factors, and help the recovery of the patient in relation to the consequences of the treatments. Two types of physical activity can be addressed in the context of breast cancer; Dance and the Pilates method. Thus, the objective of the present study will be to analyze the impact of Pilates practice and dance on quality of life and on psychological and physical factors in patients undergoing adjuvant treatment of breast cancer. Patients older than 18 years who are in adjuvant treatment, namely, chemotherapy, radiotherapy and / or hormone therapy at the Oncology Research Center - CEPON, will be invited to be part of the study. With a randomized clinical trial of three arms, the patients will be submitted to 16 weeks of intervention, and randomized in 3 groups: (A) belly dance protocol group; (B) Pilates method protocol group, and (C) control group who will continue with their routine activities. Sample randomization will be conducted in confidence by one of the researchers in a specific computer program. Information about personal and clinical characteristics, quality of life, psychological factors (depressive symptoms, body image, self-esteem, optimism, perceived stress, fatigue, pain, sexual function and sleep quality) and physical factors (cardiorespiratory fitness, balance , Posture, upper limb functionality and presence of lymphedema). All information will be collected before and after the intervention period. Statistical analysis will use the statistical package SPSS - IBM, version 20.0. Firstly, descriptive statistics (mean, standard deviation and percentage) will be used in order to know the data, and then the Anova two way test with repeated measurements and Sydak Comparison Test, in order to analyze the data. Groups of the Pilates method, of the dance and control group. Significance level of 5%.

NCT ID: NCT02478606 Completed - Range of Motion Clinical Trials

Passive Static Stretching and Proprioceptive Neuromuscular Facilitation in Musculoskeletal Aspects

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

This study investigates the influence of two different stretching techniques on the flexibility of the muscles that are in the posterior thigh, after a training period. The study will last for six weeks where the volunteers need to go to the lab twice for evaluation, and for four weeks, three times a week for the application of stretching training. Evaluation before and after the training period consists of applying hip and knee flexibility tests, evaluation of strength, muscle activation and muscle architecture. The Flexibility tests are: (1) Straight Leg Raise Flexibility Test (SLR), where the volunteer will be positioned supine on a stretcher. Then the appraiser will perform hip flexion keeping the knee extended and relaxed foot to the angle at which the person refer discomfort while the contralateral limb remain firmly leaning on the table; (2) Modified Passive knee extension (TEJ), where the volunteer will be positioned supine on a stretcher. The assessor shall determine the hip member to be rated at 90º and perform knee extension to the angle at which the person refer discomfort. The contralateral limb remain firmly leaning on the table. For the evaluation of muscle strength the volunteer had sat on equipment, makes five repetitions of bending and straightening the knee to familiarize yourself with the equipment and after will make other five replicates doing maximum strength. To evaluate the electrical activity will be the depilation of the skin with a razor and cleaning with an alcohol swab after adhesive electrodes will be placed for collection of muscle activity, the electrodes do not emit shocks. The muscle architecture will be assessed via a ultrasound , to its use the use of a water soluble gel to improve the machine's skin contact is required. For the intervention, the stretching will be held in both legs, where the volunteer will remain lying on a stretcher with fixed trunk with velcro straps and the researcher will carry out the elongation raising the leg drawn to the moment of discomfort the volunteer will refer and will remain for 30 seconds (s) in case he belongs to passive static stretching group, if the stretching group of proprioceptive neuromuscular facilitation, will be in the same position, but before the 30s of stretching, he you will have to push against during 6s to lower leg against the researcher. If he belongs to the control group, have only two trips to the laboratory for testing, will make an initial assessment and after four weeks will return to perform the tests again, in the period between assessments will not need to go to the lab because it does not make intervention elongation. It is possible that there discomfort during flexibility testing, strength testing and stretching training. After the tests can still experience muscle pain should disappear within 48 hours. The risks of research are minimal, not exceeding those of a strength training session and stretching.

NCT ID: NCT02180360 Completed - Range of Motion Clinical Trials

Capoeira Training and Flexibility

Start date: February 2012
Phase: N/A
Study type: Interventional

Background: Nowadays, a commonly used sport that helps enhancing physical fitness components, including flexibility, is Capoeira. This modality is defined as an athletic sport composed by an individual attack and defensive system, which was originally created in colonial Brazil. Capoeira is characterized by its main movement, the "ginga", and by other several dodging, unbalancing, traumatizing and acrobatic movements. The literature empirically discusses that Capoeira contributes in general physical fitness by modulating several variables of human movement. Among these variables it is possible to highlight the influence of Capoeira in the amplitude of movement of the practitioner's joints. However, no study with a control group has investigated the alterations in flexibility of beginners using an experimental protocol based exclusively in basic techniques of Capoeira, without applying any usual stretching exercises that are commonly used, independently of the specificity of the sport. Objective: To analyze the effects of eight weeks of basic training in Capoeira on the flexibility of beginners in the sport. Methods: Twenty-one individuals, divided in two groups [Capoeira, n=13; 26.1±7.2 years; 22.7±2.7 kg.m2(-1) and Control, n=8; 27.1±0.5 years; 24.3±3.3 kg.m2(-1)] participated in the study. The Capoeira group performed eight weeks of basic training (two sessions per week lasting 60 minutes each). The experimental protocol used was exclusively based in basic techniques of a programmed Capoeira training system. Before and after the intervention measurements were performed aiming to analyze: trunk flexion flexibility, through a sit-and-reach test using a Wells' Bench (WBtf); and passive tension (PThf) and maximum amplitude of hip flexion (MAhf) through goniometry. The hypothesis of this study is that the group Capoeira (beginners) will increase the linear and angular flexibility after eight weeks of basic training in the sport.

NCT ID: NCT01241071 Completed - Low Back Pain Clinical Trials

Effects of Myofascial Release on Pain, Disability and Electromyography of Erector Spinae in Chronic Low Back Pain

Start date: January 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether myofascial release techniques are effective in the improvement of pain, disability and electromyography response of lumbar muscles in patients with chronic low back pain.

NCT ID: NCT00859365 Completed - Anxiety Clinical Trials

Acupuncture for Back and Neck Pain in an Emergency Room Setting

ABNP
Start date: January 2009
Phase: Phase 1/Phase 2
Study type: Interventional

This study aims to examine the efficacy of an Integrative approach utilizing Acupuncture as an add-on therapy for the treatment back and neck pain in an emergency department setting Acupuncture is well established as an effective treatment for back pain. The investigators cumulative experience in Asaf Harofeh Medical Center has shown Acupuncture to be an Effective therapy for simple back and neck pain in an ER setting. This study will examine weather Acupuncture can decrease pain, increase range of motion and decrease anxiety in patients admitted to the Emergency Room with simple back and neck pain without neurological findings. Acupuncture will be performed as an add on therapy on top of analgesic therapy.