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Upper Extremity Problem clinical trials

View clinical trials related to Upper Extremity Problem.

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NCT ID: NCT06269887 Completed - Clinical trials for Upper Extremity Problem

Dominant Non-Dominant Upper Extremity in Gender

Start date: November 7, 2023
Phase:
Study type: Observational

There are strength and functional differences between non-dominant and dominant extremities. This is important in the hand and extremity rehabilitation process. This situation also differs between genders. Comparison of the dominant and non-dominant limb can provide important clinical or rehabilitation field-related information. It is reported in the literature that manual dexterity, grip strength and joint position sense may differ between extremities. However, the relationship between this situation and the difference between genders has not been explained. It is thought that examining this difference can be extremely useful in determining achievable goals in hand rehabilitation and in customizing care for different groups.

NCT ID: NCT06155617 Completed - Clinical trials for Upper Extremity Problem

Pain, Range of Motion, Edema, Sensibility, Strength (PRESS) & Self-reported Function Create a Comprehensive Score

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

The aim of this study is to examine the development of a conceptual framework and provide evidence for reliability of a comprehensive hand therapy evaluation score. This approach provides a new standardized tool for upper extremity (UE) evaluation. Components of Pain, Range of Motion (ROM), Edema, Sensibility, Strength (PRESS), and self-reported Function were combined to create a baseline. Each assessment tool used for the PRESS to Function Approach assists in determining appropriate interventions.

NCT ID: NCT06122740 Completed - Stroke Clinical Trials

Reliability and Validity Studies of Turkish Version of Manual Ability Measure-36

Start date: July 15, 2016
Phase:
Study type: Observational [Patient Registry]

This study aim was to investigate the validity and reliability of Turkish version of Manual Ability Measure-36 (MAM-36) in patients with neurological disease.

NCT ID: NCT06004648 Completed - Clinical trials for Upper Extremity Problem

Comparison of Selective Trunk and Supraclavicular Brachial Plexus Blocks

Start date: July 28, 2022
Phase:
Study type: Observational

There are different methods in brachial plexus blocks for hand, wrist, forearm, and elbow operations. In this study, the anesthetic efficacy of the ultrasound-guided selective truncus methods and the supraclavicular methods for brachial plexus blocks in upper extremity surgeries will be compared.

NCT ID: NCT05980078 Completed - Clinical trials for Upper Extremity Problem

Interactive Informed Consent and Decision Conflict

Start date: November 1, 2017
Phase: N/A
Study type: Interventional

Informed consent for surgery can address the legal aspects while also being simple, informative, and empathic. It can help people confirm that the potential harms are acceptable in light of the potential benefits. Standard consent forms just document this process, while a computer-based, interactive consent process can also standardize and potentially enhance it.

NCT ID: NCT05872646 Completed - Clinical trials for Cognitive Impairment

The Effect of Cognitive Functions on Upper Extremity Functionality in Parkinson's Patients

Start date: February 8, 2018
Phase: N/A
Study type: Interventional

Parkinson's Disease (PD), first described by James Parkinson in 1817, is a progressive movement disorder that develops mainly as a result of the destruction of nigrostriatal dopaminergic neurons. The aim of our study is to determine the effect of cognitive functions on upper extremity functionality in individuals with Parkinson's Disease.

NCT ID: NCT05821257 Completed - Multiple Sclerosis Clinical Trials

Arm Swing During Walking in Early Multiple Sclerosis

Start date: December 1, 2021
Phase:
Study type: Observational

Multiple sclerosis (MS) is the most common central nervous system inflammatory demyelinating disease which causes motor and sensory deficits, cerebellar symptoms, and balance problems. Due to these symptoms, gait abnormalities are common in MS, even in patients with low degrees of impairment. The upper limb has an important role on postural control and gait stability. Affected arm swing movement and asymmetry during gait are common in neurological disorders such as Parkinson's disease (PD) even in early stages of the disease and arm swing treatment has been acknowledged to enhance gait and normalize arm swing in individuals with PD. The presence of arm swing changes during walking in MS patients, similar to PD, especially in the early period, may be an indicator of balance problems, this was, however, not investigated as such. Therefore, the aim of the current study is to assess the arm swing during gait in people with MS shortly after their diagnosis in early MS.

NCT ID: NCT05662878 Completed - Stroke Clinical Trials

Evaluation of Hand Strength and Spasticity in Hemiplegic Patients

Start date: October 15, 2022
Phase:
Study type: Observational

The aim in this study is to evaluate spasticity and hand grip strength with a finger hand robot in the Turkish population.

NCT ID: NCT05274555 Completed - Clinical trials for Duchenne Muscular Dystrophy

Reliability and Validity of the Turkish Version of the Upper Limb Short Questionnaire in Duchenne Muscular Dystrophy

Start date: March 27, 2019
Phase:
Study type: Observational

Purpose: This study aimed to evaluate the construct validity and reliability of the Turkish version of the Upper Limb Short Questionnaire (ULSQ) in Duchenne muscular dystrophy (DMD). Materials and methods: A total of 41 children with DMD have participated in the study. Upper and lower extremities functional levels were assessed with Vignos Scale and Brooke Upper Extremity Functional Rating Scale, respectively. The construct validity of the questionnaire was determined using the correlation between the ULSQ and ABILHAND-Kids. The Cronbach alpha value was calculated to determine internal consistency. To determine test-retest reliability, 17 randomly selected children were evaluated seven days after the first evaluation, and the "Intraclass Correlation Coefficient (ICC)" value was calculated.

NCT ID: NCT05239520 Completed - Shoulder Pain Clinical Trials

Understanding Control and Mechanisms of Shoulder Instability in FSHD

Start date: March 25, 2022
Phase:
Study type: Observational

The aim of this study is to identify factors for shoulder instability in people with Facioscapulohumeral dystrophy (FSHD). FSHD is a non-life limiting condition with symptoms presenting in the second decade of life (Evangelista et al., 2016). Between 2500 to 3000 people are diagnosed with FSHD in the UK and it is the third most common dystrophy. The overall prevalence is 1: 20,000 and on average 52 people are newly diagnosed with FSHD each year (Emery, 1991; Padberg et al., 1995; UK, 2020) As the disease progresses, patients lose the ability to adequately control muscles around the shoulder girdle, possibly contributing to the development of shoulder instability i.e. partial or complete dislocation of the shoulder joint (Bergsma, Cup, Geurts, & De Groot, 2015; Bergsma, Cup, Janssen, Geurts, & de Groot, 2017; Mul et al., 2016). Loss of control around the shoulder is also thought to contribute to pain and a reduced capacity to perform tasks above shoulder height. Additionally, the development of fatigue and chronic pain further limit patient's abilities and engagement with rehabilitation. If we better understand the mechanisms associated with instability, we can better target physiotherapy interventions to improve rehabilitation. If we identify specific patterns of activity associated with instability, these could be addressed through personalised and improved exercise prescription and rehabilitation. Additionally, we may identify causes of instability for which physiotherapy or exercise programmes may not be appropriate, therefore ensuring patients are referred to the correct service in a timely manner, improving patient outcomes and allocating resources more appropriately.