Trigger Point Pain, Myofascial Clinical Trial
Official title:
Neurophysiological, Biomechanical and Clinical Effects of Dry Needling Versus Sham Needling When Applied to the Infraspinatus Muscle in People With Chronic Shoulder Pain: a Randomized Pilot Study
Verified date | March 2020 |
Source | Université de Sherbrooke |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Up to 77% of patients with chronic shoulder pain have a trigger point (TrP) in the
infraspinatus muscle. These TrPs can lead to pain, limitation of activities and reduced
quality of life. Dry needling (DN) is gaining popularity as a treatment for TrPs in
physiotherapy. However, its clinical effects remain poorly understood mechanistically and its
neurophysiological effects little studied.
The primary objective of this study is to determine the feasibility of a larger scale study.
The secondary objective of this study is to to explore the immediate neurophysiological,
biomechanical and clinical effects of DN and sham needling when applied to TrP of the
infraspinatus muscle in people with chronic non-traumatic shoulder pain.
Status | Completed |
Enrollment | 21 |
Est. completion date | December 20, 2019 |
Est. primary completion date | December 20, 2019 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 65 Years |
Eligibility |
Inclusion Criteria: 1. Unilateral, chronic non-traumatic shoulder pain (VAS = 2/10; >3 months) 2. Localized pain in the shoulder region or referred according to the territory of the infraspinatus (Travell and Simons, 1999) 3. Presence of a palpable nodule inside a tight muscle band reproducing the patient's pain Exclusion Criteria: 1. Cancer or metastasis in organs or tissues above the pelvis (< 5 years) 2. Shoulder capsulitis 3. Shoulder, thorax or mastectomy surgeries 4. Shoulder bone fracture (< 6 months) 5. C4-C5 or C6 radiculopathy 6. Osteoporosis or excessive atrophy of the infraspinous fossa (infraspinatus <10 mm) 7. Body mass index (BMI) > 28 Exclusion (TMS security): 1. Pregnant woman 2. Neurological, psychiatric or epilepsy conditions 3. Implants (e.g. Neurostimulator, pacemaker, cerebral aneurysm clip, screw or plate), metallic foreign body in the eye 4. Head trauma with loss of consciousness |
Country | Name | City | State |
---|---|---|---|
Canada | Centre de Recherche sur le Vieillissement | Sherbrooke | Quebec |
Lead Sponsor | Collaborator |
---|---|
Université de Sherbrooke | Centre de recherche du Centre hospitalier universitaire de Sherbrooke, Ordre Professionnel de la Physiothérapie du Québec (OPPQ) |
Canada,
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* Note: There are 35 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Recruitment rate | Average number of participants recruited per month | Through study completion, an average of 10 months | |
Primary | Exclusion rate | Number of participants excluded from the study due to eligibility criteria (e.g. too narrow, are they clear) | Through study completion, an average of 10 months | |
Primary | Refusal rate | Number of participants who refused to participate (e.g. fear of needle, fear of transcranial magnetic stimulation) | Through study completion, an average of 10 months | |
Primary | Retention rate | Number of loss at follow-up | Baseline, immediately after and 24 hours post-treatment evaluation | |
Primary | Length of time of the procedure | Average time needed per participant (testing and intervention) | Baseline, immediately after and 24 hours post-treatment evaluation | |
Primary | Safety of the procedure: adverse effects | Listing of any adverse effects | Immediately after intervention to 24 hours post-treatment | |
Secondary | Corticospinal excitability of the infraspinatus | Tested with transcranial magnetic stimulation (TMS) connected to a neuronavigation device, characterized by the active motor threshold and expressed in stimulator maximum power percentage | At baseline, immediately after intervention, 24 hours after the intervention | |
Secondary | Glenohumeral arthrokinematics | Captured images are taken using ultrasound imaging (GE Logiq-e; linear array 5-12MHz) at 0° and 30° of external rotation. Measurements in cm included: 1) subacromial space (position of the humeral head relative to the acromion); 2) anteroposterior position of the humeral head relative to the glenoid. | At baseline, immediately after intervention, 24 hours after the intervention | |
Secondary | Pressure pain perceived | Obtained using an algometer (directly applied on the TrP; average of three measurements taken at 30 sec. interval), characterized by the threshold of discomfort and expressed in kg. | At baseline, immediately after intervention, 24 hours after the intervention |
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