Myofascial Pain Clinical Trial
— KT/TrP/TMDOfficial title:
Evaluation of the Effectiveness of Kinesiotaping and Inactivation of Trigger Points in Chronic Myofascial Pain of Temporomandibular Joint Dysfunction
Verified date | January 2018 |
Source | Pomeranian Medical University Szczecin |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
In patients with a long-lasting TMD syndrome, especially of a muscular nature, palpation examination can locate the trigger points of pain (TrP) in the chewing muscles, i.e., the nodules in the shape of bumps the size of rice or pea grains. Kinesiotaping (KT) is considered as an intervention method that can be used to release latent myofascial trigger points. It is a method that involves applying specific tapes to the patient's skin surface in order to use the natural self-healing processes of the body. The aim of the study was to evaluate the effect of Kinesiotaping methods and inactivation of Trigger Points on nonpharmacological elimination of pain in patients with functional disorders of the masticatory motor system.
Status | Completed |
Enrollment | 60 |
Est. completion date | September 30, 2017 |
Est. primary completion date | June 15, 2017 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 35 Years |
Eligibility |
Inclusion Criteria: - Age between 18-35 years, both male and female - Provide informed consent to participate in the study; - Having a diagnosis of muscular pain TMD(Temporomandibular Disorders) according to group -I A, axis I RDC/TMD(Research Diagnostic Criteria) - Visual analogic scale (VAS) score from 4 to 10 for 14 days - Not have history of alcohol or drugs abuse within the past 6 months as self-reported - Not use ot carbamazepine (or similar) within the past 6 months as self reported - Not have history of neurosurgery as self-reported - Not have history of major psychiatric disorders such as schizophrenia and bipolar disorder - Not have any other previously diagnosed disorder with symptoms similar to the TMD, such as fibromyalgia. Exclusion Criteria: - One absence during therapeutic sessions; |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Pomeranian Medical University Szczecin | Ministry of Health, Poland |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | 1. Patient Global Impression of Change Scale (PGICS) | The Patient Global Impression of Change Scale (PGICS) is an understandable, adequate, easy-to-use instrument capable of measuring the perception of change in health status and satisfaction with the treatment of individuals with chronic musculoskeletal pain. It is a one-dimensional measurement instrument in which individuals rate their improvement associated with intervention on a 7-item scale ranging from 1 (no change) to 7 (Much better). | 3 months | |
Primary | 1. Change from baseline in Visual Analogic Scale | The visual analogic scale allows us to convert subjective sensations as pain on numerical data. A 10cm scale where 0cm is no pain and 10cm the worse imaginable pain, will be used and the subjects will be asked to mark a point on the scale representing their pain. This instrument will be used to compare the VAS values before and after the intervention. | 14 days |
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