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Spasticity and pain, particularly int he shoulder region, are the most common impairments experienced by subjects who had experienced a stroke. There is preliminary evidence supporting the role of dry needling for spasticity in patients who had suffered from a stroke. Few data exists on the effects on shoulder pain. In addition, it has been shown that application of dry needling induces post-needling soreness in individuals with musculoskeletal pain. No previous study has investigated the presence and the duration of post-needling soreness in individuals who had experienced a stroke.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Dry needling | Experimental | The experimental group will receive a single session of modulatory interventions combined with a single session of dry needling into the shoulder muscles which active trigger points will reproduce the shoulder pain symptoms. |
|
| Physical Therapy | Active Comparator | This group will receive a single session of modulatory interventions targeting modulation of central nervous system. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Dry Needling | Other | A single session of modulatory interventions combined with a single session of dry needling into the shoulder muscles which active trigger points will reproduce the shoulder pain symptoms. |
| Measure | Description | Time Frame |
|---|---|---|
| Changes in post-dry needling pain intensity with a numerical pain rate scale before and after the intervention | A Numerical Pain Rate Scale (NPRS, 0-10) will be used to record post-dry needling soreness in the targeted area | Baseline, 24 hours (1 day) after and 72 hours (3 days) after treatment the intervention |
| Measure | Description | Time Frame |
|---|---|---|
| Changes in spontaneous shoulder pain with a numerical pain rate scale before and after the intervention | A Numerical Pain Rate Scale (NPRS, 0-10) will be used to assess spontaneous shoulder pain | Baseline, 72 hours (3 days) and 168 hours (7 days) after treatment the intervention |
| Presence of active trigger points in the shoulder musculature |
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Inclusion Criteria:
Exclusion Criteria:
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| César Fernández-de-las-Peñas | Alcorcón | Madrid | 28922 | Spain |
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| ID | Term |
|---|---|
| D020521 | Stroke |
| ID | Term |
|---|---|
| D002561 | Cerebrovascular Disorders |
| D001927 | Brain Diseases |
| D002493 | Central Nervous System Diseases |
| D009422 | Nervous System Diseases |
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| ID | Term |
|---|---|
| D000079245 | Dry Needling |
| D026741 | Physical Therapy Modalities |
| ID | Term |
|---|---|
| D000529 | Complementary Therapies |
| D013812 | Therapeutics |
| D012046 | Rehabilitation |
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| Physical Therapy | Other | A single session of modulatory interventions targeting modulation of central nervous system. |
|
Manual palpation of active trigger points in the shoulder muscles will be conducted |
| Baseline, 72 hours (3 days) and 168 hours (7 days) after treatment the intervention |
| D014652 | Vascular Diseases |
| D002318 | Cardiovascular Diseases |