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Muscle Pain clinical trials

View clinical trials related to Muscle Pain.

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NCT ID: NCT06006481 Completed - Muscle Pain Clinical Trials

Musculoskeletal Problems and Strategies Developed by Physiotherapists to Cope With Them

Start date: September 1, 2023
Phase:
Study type: Observational

The aim of this study is to investigate whether there is a difference in areas such as occupational musculoskeletal injuries and strategies developed by physiotherapists working in different fields, burnout and occupational satisfaction.

NCT ID: NCT05812209 Completed - Pain Clinical Trials

Stellate Ganglion Block to Treat Long COVID 19 Case Series

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

An assessment of the effectiveness of Stellate Ganglion Block in alleviating symptoms of Long COVID-19.

NCT ID: NCT05625945 Completed - Clinical trials for Cardiovascular Diseases

Physical Activity Levels and Statin Therapy

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

Rationale: Combining statin treatment and physical activity is very effective for the prevention of cardiovascular diseases. Statins are well-tolerated by most patients, but may cause statin-associated muscle symptoms (SAMS). Objective: To identify predictors for SAMS in statin users and to objectively assess physical activity levels and sedentary time between symptomatic and asymptomatic statin users.

NCT ID: NCT05601843 Completed - Acute Pain Clinical Trials

Transcutaneous Electrical Nerve Stimulation for Back Pain in the Emergency Department (TENS-ED)

TENS-ED
Start date: May 8, 2023
Phase: N/A
Study type: Interventional

The effectiveness of Transcutaneous Electrical Nerve Stimulation (TENS) to reduce pain scores for patients with acute back pain in an ambulatory emergency department (ED) population will be examined in this dual-center, cluster randomized, controlled, open-label study.

NCT ID: NCT05378984 Completed - Muscle Pain Clinical Trials

Cocoa Intake and Muscle Pain Sensation

Start date: March 1, 2020
Phase: N/A
Study type: Interventional

This experimental randomized, double-blind, and controlled study included fifteen young, healthy, and pain-free men and 15 age-matched women. It lasted for three visits with at least one-week washout. Pain was experimentally induced, twice at each visit, with intramuscular injections of 0.2 mL hypertonic saline (5%), before and after intake of one of the different chocolate-types; white (30% cocoa-content), milk (34% cocoa-content), dark (70% cocoa-content). Pain duration, pain area, peak pain, and pressure pain threshold were assessed every fifth minute after each injection, between the time-points 5 to 30 min. Prior to inclusion, all participants underwent an examination in a dental chair. This included a clinical examination of the orofacial region according to the Diagnostic Criteria for temporomandibular disorders (DC/TMD) by a blinded examiner. Participants were also examined regarding their psychosocial status prior to inclusion, this included depression, somatization, anxiety, pain catastrophizing and stress.

NCT ID: NCT04717518 Completed - Neck Pain Clinical Trials

Anchoring Patients Pain Scores in the Emergency Department

Start date: August 24, 2020
Phase:
Study type: Observational

The proposed research will be a prospective, observational study to test the hypothesis that anchoring will affect verbal pain scores in the emergency department. There will be a small retrospective aspect to this study to obtain patient satisfaction ratings.

NCT ID: NCT04453215 Completed - Clinical trials for Systemic Lupus Erythematosus

Laser Therapy for Patients With Systemic Lupus Erythematosus

Start date: January 12, 2019
Phase: N/A
Study type: Interventional

Systemic lupus erythematosus (SLE) is a chronic, autoimmune disease that has detrimental effects on connective tissue and other organs. The musculoskeletal system is one of the most affected systems in this group of patients including the temporomandibular joint. The most common symptoms when muscle involvement in SLE are muscle atrophy decreased muscle strength and myopathy. SLE activity and long-term corticosteroid use are thought to be responsible for these symptoms, thus, SLE patients are accepted to be at higher risk for temporomandibular joint disorders (TMD). Low-level laser therapy(LLLT) is frequently used in the treatment of TMD due to its pain relief and anti-inflammatory effect. Thus, in this study, LLLT has been used to evaluate this treatment modality on the chewing function and pain values of SLE patients with myogenic TMD.

NCT ID: NCT04390438 Completed - Knee Pain Chronic Clinical Trials

Efficacy of High and Low Intensity Percutaneous Electrolysis for the Treatment of Myofascial Pain Syndrome

Start date: February 17, 2020
Phase: N/A
Study type: Interventional

Muscle pain is frequently attributed to myofascial pain syndrome (MPS) in which myofascial trigger points (MTrP) are a characteristic feature. Dry needling is a frequent clinical practice to manage MPS but few evidence is published about percutaneous electrolysis effects for the treatment of MPS. This is a randomized clinical trial with 3 parallel groups: 1) High intensity-short time percutaneous electrolysis; 2) Low intensity-long time percutaneous electrolysis; 3) dry needling control group.

NCT ID: NCT03831737 Completed - Muscle Pain Clinical Trials

Team-based Ergonomics Educational Model for Workplace WELLNESS Improvement: A Pilot Study

TEEM WELLNESS
Start date: February 11, 2019
Phase: N/A
Study type: Interventional

This research is being done to explore the potential benefit of a physical therapist-guided stretching program on musculoskeletal pain and well-being.

NCT ID: NCT03044106 Completed - Muscle Weakness Clinical Trials

Cranial Laser Reflex Technique for Hamstring Function

CLRTHam
Start date: March 4, 2017
Phase: N/A
Study type: Interventional

Purpose: To conduct a pilot study of the effect of Cranial Laser Reflex Technique (CLRT) compared with sham laser on hamstring muscle flexibility, strength, and pain pressure threshold. Participants: Active, young adults ages 18 to 35. Procedures: A two-visit, assessor and participant-blinded crossover study with 1-week washout. Subjects will complete three functional hamstring tests before and after CLRT and sham laser treatment. Subjects will also complete questionnaires to assess their expectations and perceptions of the interventions.