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Musculoskeletal Diseases clinical trials

View clinical trials related to Musculoskeletal Diseases.

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NCT ID: NCT04156867 Completed - Clinical trials for Orthopedic Disorder of Spine

Evaluation of Outcomes of Discectomy With Dynesys in Treatment of Lumbar Disc Herniation

Start date: August 1, 2014
Phase: N/A
Study type: Interventional

To explore the clinical outcomes of discectomy with dynamic neutralization system(Dynesys) on treatment of single-segmental lumbar disc herniation(LDH) versus simple discectomy.

NCT ID: NCT04152538 Recruiting - Clinical trials for Musculoskeletal Disorder

Changes in Quadriceps Muscular Activity in Patients After Total Knee Arthroplasty Compared to Healty Subjects

Start date: July 15, 2019
Phase:
Study type: Observational

During Total Knee Arthroplasty (TKA), joint undergo considerable stress, which causes neuromuscular activation deficits of the quadriceps femoris muscle.The aim of the study is to investigate differences in quadriceps neuromuscular activity in the acute phase after surgery.

NCT ID: NCT04138264 Completed - Orthopedic Disorder Clinical Trials

Opioid Counseling Following Orthopaedic Surgery

Start date: June 19, 2018
Phase: N/A
Study type: Interventional

Postoperative pain management and opioid consumption following outpatient orthopaedic surgery may be influenced by a number of variables including knowledge of safe opioid use. A prospective randomized study is designed to understand the effect of preoperative opioid counseling on postoperative opioid consumption and the typical opioid consumption patterns following common outpatient orthopaedic surgeries. The hypothesis was that patients who received preoperative opioid counseling will consume less postoperative opioid medication and experience greater satisfaction with pain management.

NCT ID: NCT04135976 Completed - Clinical trials for Musculoskeletal Diseases or Conditions

Applicability of the ICF in Primary Care Physiotherapy Units in the Health Service of Castille and Leon (Spain)

Start date: June 1, 2020
Phase:
Study type: Observational [Patient Registry]

The primary care physiotherapy units of the Spanish health service in Castille and Leon (SACYL) are responsible for providing physiotherapy treatments to the general population. Being part of the primary health care system, the actions of these units are aimed at the treatment of common conditions that do not involve severity, frequently musculoskeletal disorders. The work of physiotherapists is closely related to the functionality of patients and, in this sense, the World Health Organization (WHO) has proposed the International Classification of Functioning, Disability and Health (ICF) as a conceptual framework to characterize the functional status of individuals. The use of ICF in the clinical setting is not sufficiently widespread due to the the difficulties that the use of such an exhaustive classification implies in practice. In an attempt to address this problem, the WHO has encouraged the development of reduced versions aimed at responding to specific conditions or care contexts. The idea behind the development of core sets is that it is possible to select a number of categories so as to capture the essence of a given clinical process, allowing an agile use of the ICF. However, in order to put these core sets into practice, it is necessary to check that the selected categories are valid from the perspective of the participants in the clinical processes. The purpose of this research project is to determine whether the musculoskeletal core sets of the ICF are applicable in SACYL primary care physiotherapy units. This implies knowing if the categories already selected in these sets are representative of the health aspects considered as most relevant in the clinical context of physiotherapy in primary care. To achieve this, four studies will be conducted to capture the perspective of patients, physiotherapists, researchers and clinical practice. This information will be translated into the language of the ICF to obtain comparable categories with those present in the core sets. In this way, this research project will make possible to validate or adapt the core sets of the ICF for musculoskeletal conditions, in a specific clinical context of physiotherapy in primary care.

NCT ID: NCT04102059 Not yet recruiting - Work-related Injury Clinical Trials

Pattern of Work Related Musculoskeletal Disorders Among Nurses at Main Assiut University Hospital

Start date: December 2019
Phase:
Study type: Observational

The term work-related musculoskeletal disorders (WRMDs) is defined according to the World Health Organization (WHO), as a wide range of inflammatory and degenerative diseases and disorders that result in pain and functional impairment. They arise when individuals are exposed to work activities and conditions that significantly contribute to their development or exacerbation, but which may not be their sole cause (1,2). Another definition The National Institute for Occupational Safety and Health defined WRMDs as "an injury of the muscles, tendons, ligaments, nerves, joints, cartilage, bones, or blood vessels in the arms, legs, head, neck, or back that is caused or aggravated by work tasks such as lifting, pushing, and pulling(3-5). They represent the second largest cause of short‑term or temporary work disability after the common cold (6).Apart from lowering the quality of workers' life and reducing the productivity, WRMDs are the most expensive form of work disability, attributing to about 40% of all costs toward the treatment of work‑related injuries(7). It is estimated that almost one-third of all cases of sick leave among health care workers are related to musculoskeletal disorders(8).According to the Bureau of Labor Statistics (BLS) in 2013, WRMDs cases accounted for 33% of all worker injury and illness cases(9). Most WRMSDs develop over time with usually, no single cause but various factors work in combination. According to the European Occupational Safety and Health Agency (EU-OSHA), the most common physical causes and organizational risk factors of musculoskeletal disorders (MSDs) include: - Prolonged sitting or standing in the same position - Performing the same task over and over - Continuing work while injured - Awkward and static postures - Load handling, especially when bending and twisting - Repetitive or forceful movements - Vibration - Insufficient work breaks(7,10-12).

NCT ID: NCT04093856 Completed - Obesity Clinical Trials

Determinants of Bone and Muscle Quality and Strength in Obesity With and Without Diabetes

BODI2
Start date: January 14, 2020
Phase:
Study type: Observational

Background: Osteoporotic fractures are a major public health issue. They cause substantial disability, loss of autonomy, morbidity and excess mortality. Diabetes is also associated with increased risk for falls and fractures through a direct impact of elevated blood glucose on the skeleton and on muscles. Research project overview: The investigators propose a cross-sectional study that will involve 2 research centers in the province of Quebec. The investigators will recruit 20 obese participants, without diabetes, who have not undergone bariatric surgery, for one-time measurements to be compared with baseline measurements (pre-surgery) from participants in the bariatric obese diabetic groups with type II diabetes mellitus from the ongoing study BODI study (NCT03455868). Bone Mineral Density as well as muscle quality, strength and function will be evaluated at a single study visit. Relevance: This data will permit the evaluation of the bone-muscle unit in patients with obesity with and without diabetes, and assess whether the presence and duration of diabetes impacts further on clinical and functional musculoskeletal outcomes (falls, fractures and mobility and strength) in this population. AGEs, if associated with muscle and bone deterioration, might become an easily accessible biomarker of musculoskeletal health in the clinical setting.

NCT ID: NCT04092946 Completed - Clinical trials for Musculoskeletal Diseases

Digital Home-based Rehabilitation for Musculoskeletal Disorders

Start date: June 16, 2020
Phase: N/A
Study type: Interventional

The purpose of this study is to assess the acceptance, engagement and outcomes of a digital care program for acute and chronic musculoskeletal conditions affecting the shoulder, elbow, hip, knee, ankle and spine.

NCT ID: NCT04090372 Completed - Orthopedic Disorder Clinical Trials

Digital Preop-planning of Total Hip Arthroplasties

PLANORTHO
Start date: January 8, 2020
Phase: N/A
Study type: Interventional

Residual leg length discrepancy is a common issue after total hip arthroplasty(THA). Digital preoperative planning may improve the accuracy of the surgical procedure and may help the surgeon to precisely predict implants sizes

NCT ID: NCT04078880 Completed - Anemia Clinical Trials

Iron Supplementation in Hip/Knee Surgery

Start date: December 4, 2018
Phase: N/A
Study type: Interventional

Randomized controlled trial to evaluate the efficacy of oral iron supplementation in reducing the prevalence of preoperative anemia in a cohort of 82 patients undergoing elective prosthetic hip or knee surgery.

NCT ID: NCT04074382 Active, not recruiting - Surgery Clinical Trials

FIT Study (Functional Outcomes In Trauma Study)

Start date: August 10, 2020
Phase:
Study type: Observational [Patient Registry]

Why? There is not much information in the UK on how well patients who sustain major trauma function afterwards. Major trauma is defined as significant injuries with a calculated 'injury severity score' (ISS) over 15. The ISS is calculated based on how many parts of the body are injured and how badly injured these are, up to a maximum score of 75 (fatal). We feel that learning more about how these people cope afterwards, and what influences this will allow us to improve the care we can deliver in the future, which will hopefully lead to better outcomes. What? We propose to implement the FIT (Functional outcomes In Trauma) study to assess how well patients function physically, psychologically and socially, and get back to activities of daily living, work and participation in recreational activities following major trauma. Who? Major trauma patients: 2 cohorts: prospectively going forwards in time (from baseline to 12 months after trauma) and retrospectively going backwards in time (patients between 2-10 years after trauma). Where? Leeds General Infirmary. How? We will do this by collecting data from questionnaires completed by patients (also known as PROMS, or Patient Reported Outcome Measures), using an online questionnaire service developed at the University of Leeds, called QTool. These will offer the participants the chance to tell us how they are doing across lots of areas, with both tick-box multiple choice questions and open-ended questions to explain how they are doing and what influences this. We will also interview a random selection of patients in further detail to discuss how their trauma has affected them, how they found the study, how we could improve it. Afterwards we will send participants a copy of what we have learnt from the study and aim to publish it in a scientific journal. Timeline/Phase overview: The FIT Study will consist of 2 phases. Phase 1 will last for 2 years in total (12 months for prospective study cohort recruitment and 12 months follow-up for these patients) during which time data will be collected from the retrospective cohort as well. Following this there will be a full analysis of the data, after which phase 2 of the FIT Study will begin. Patients enrolled into phase 1 of the study will be given the option of consenting to being contacted annually to complete the same set of online PROMs, which will comprise phase 2 of the study. We will also continue active recruitment into both prospective and retrospective arms of the study in phase 2. We plan to continue data collection on an annual basis up to 10 years post trauma in phase 2 of the study for patients in both cohorts. We hope to incorporate elements of the FIT Study into future routine care with what we learn from the FIT Study, and develop our own unique Patient Reported Outcome Measure tool, with the overall aim of improving patient care and outcomes.