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Upper Extremity clinical trials

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NCT ID: NCT06244030 Completed - Exercise Addiction Clinical Trials

The Effect of Core Stabilization Exercises in Female Wrestlers

Start date: February 5, 2024
Phase: N/A
Study type: Interventional

This study was planned to investigate the effect of core stabilization exercise program on trunk muscle strength, spinal stability and upper extremity performance in elite wrestling athletes.

NCT ID: NCT06167382 Completed - Healthy Adults Clinical Trials

The Effect of Arm Ergometer Exercise on Dexterity

Start date: December 25, 2022
Phase: N/A
Study type: Interventional

The goal of this single group assessment study is to investigate acute effect of arm ergometer exercise intensity on dexterity and hand reaction time in healthy male or female participants aged 18-35. - Knowing the acute effect and change of hand dexterity and reaction times of individuals with arm ergometer intensities applied at different intensities provides us with data that can be processed and used in neurological, orthopedic patient groups and geriatric cases during the rehabilitation process. - The positive gains enable us to obtain effective and observable results in the rehabilitation progression of individuals and in parameters such as muscle strength and endurance, quality of life, depression, chronic pain. Participants who accepted the voluntary basis will be taken and the Physical Activity Readiness Questionnaire for Everyone (PAR-Q+) will be filled. After all evaluations were made to the participants, 3 different exercise intensities; maximum heart rates; 60%, 70%, 80% will do arm ergometer exercises. - ROM measurements - Muscle strength tests - Grip strength measurement (Jamar hand dynamometer) - Dexterity and Function tests (Nelson Hand Reaction Test - Purdue Pegboard Test - Minnesota Manual Dexterity Test) evaluation parameters will be applied before, immediately after and 15 minutes after each exercise intervention.

NCT ID: NCT05258344 Completed - Breast Cancer Clinical Trials

Reliability and Validity of The '6 Minute Pegboard and Ring Test' in Patients With Breast Cancer

Start date: March 1, 2022
Phase:
Study type: Observational

Breast cancer is one of the most common cancers among women in the world and its incidence reaches up to 16%.Although survival can be increased with early diagnosis and more effective therapies, physical complications such as lymphedema, upper extremity dysfunction and chronic pain are frequently seen during and/or after breast cancer treatments. It has been determined that lymphedema associated with breast cancer treatment is a factor that mediates and/or exacerbates the adverse effects of breast cancer treatments on upper extremity functional capacity and quality of life of patients.It was determined that the 6 Minute Pegboard and Ring Test (6PRT) score showed a clear relationship with the upper extremity daily living activities (ADLs), and it was concluded that the 6 Minute Pegboard and Ring Test (6PRT) test could be used as an appropriate test in pulmonary rehabilitation programs to predict and show the improvement of daily living activities (ADLs). Therefore, in this study; The results to be obtained by evaluating the validity and reliability of the 6 Minute Pegboard and Ring Test (6PRT) test in breast cancer patients will increase the use of this test in both testing arm endurance and arm exercise capacity in breast cancer patients, and predicting the effect on daily living activities (ADLs)

NCT ID: NCT05205278 Completed - Clinical trials for Physical Performance

Effect of Progressive Isolated Core Stability Training

Start date: September 1, 2012
Phase: N/A
Study type: Interventional

Forty-two adolescent female volleyball athletes (16.0±1.4 years) were randomly divided into two groups. Group 1 was the training group and, in addition to the routine volleyball training programmes, underwent an 8-week (3 days/week) progressive core stability training programme. Group 2 was the control group and only did routine volleyball training, with no core stability training. Main outcome measures: Shoulder IR and ER strength, medicine ball throw (MBT), modified push up (MPU) and closed kinetic chain (CKC) upper extremity stability tests were used to evaluate physical performance.

NCT ID: NCT05119803 Completed - Quality of Life Clinical Trials

The Relationship of Spine Posture and Mobility With Upper Extremity Functions in Parkinson's Patients

Start date: November 3, 2021
Phase:
Study type: Observational

The aim of this study is to investigate whether spinal alignment and spinal mobility have an effect on upper extremity functions in Parkinson's patients. In the light of the data obtained as a result, we think that our study will also contribute to determining the factors that may cause upper limb dysfunctions seen in Parkinson's patients and will guide new treatment-oriented studies to be carried out in the future.

NCT ID: NCT05114629 Completed - Electromyography Clinical Trials

Biomechanics of Adaptive Rowing in Active and Inactive Manual Wheelchair Users

Start date: September 14, 2021
Phase:
Study type: Observational

This research is being performed to characterize the rowing stroke in active and inactive individuals who use a manual wheelchair. The investigators will be looking at muscle activity of four shoulder muscles (upper trapezius, lower trapezius, serratus anterior, and posterior deltoid) and motion of the arms, shoulder blade, and trunk during rowing. This will be done for three rowing conditions (1: adapted rowing ergometer, 2: rowing ergometer from a chair, 3: standard seated row exercise using an elastic band [TheraBand]). The investigators are also looking at shoulder strength, range of motion, quality of life, and community participation.

NCT ID: NCT04669847 Completed - Clinical trials for Muscular Dystrophy, Duchenne

The Effects of Trunk Exercises on Upper Extremity and Respiratory Functions in DMD

Start date: April 7, 2018
Phase: N/A
Study type: Interventional

The aim of this study was to investigate the effects of trunk training on trunk control, upper extremity, and pulmonary function in children with Duchenne muscular dystrophy (DMD). 26 children with DMD aged 5-16 were included in the study. They were divided into two groups (study and control). The study group exercised with the trunk-oriented exercise program and the conventional exercise program under the supervision of a physiotherapist, whereas the control group underwent the conventional exercise program under the supervision of their families at home for 8 weeks. Trunk control, the upper extremity function and respiratory function test were assessed before and after the 8-week exercise program in this study.

NCT ID: NCT03378323 Completed - Upper Extremity Clinical Trials

Single Versus Multiple Injections for Axillary Plexus Block

Start date: July 1, 2018
Phase: Phase 4
Study type: Interventional

Patients will be randomized to one of two groups: 1. Multiple injection group: Axillary brachial plexus block with multiple injections, with the arm abducted, performed with the aid of ultrasound; 2. Single injection group: Axillary brachial plexus block with a single injection, with the arm placed behind the head and the elbow flexed, performed with the aid of ultrasound

NCT ID: NCT03318341 Completed - Stroke Clinical Trials

TheraBracelet Phase I

Start date: January 9, 2018
Phase: N/A
Study type: Interventional

This project aims to test a new technology that may improve hand function impaired from a stroke, thereby improving independence and quality of life.

NCT ID: NCT01075503 Completed - Upper Extremity Clinical Trials

Clinical Research of Retrograde Infraclavicular Brachial Plexus Blockade

RIBPA
Start date: March 2008
Phase: N/A
Study type: Interventional

Brachial plexus block is a frequently used technique for upper extremity surgery. All present approaches and techniques have certain advantages and disadvantages. It's necessary to develop a new approach to brachial plexus block which 1) provides reliable anesthesia, 2) is easy to perform, 3) isn't restricted by posture, 4) provides extensive sensory distribution, 5) causes as few complications as possible, 6) easily place a secured catheter for post-operative analgesia. The investigators established the retrograde infraclavicular brachial plexus block approach. The investigators compared and verified the feasibility, efficacy and safety of this new approach with other classic approaches to brachial plexus block.