Subacromial Impingement Clinical Trial
Official title:
Effectiveness of High Intensity Laser Therapy in the Treatment of Subacromial Impingement Syndrome
Verified date | March 2017 |
Source | University of Castilla-La Mancha |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of this study is to assess the effectiveness of high intensity laser therapy in the treatment of subacromial impingement syndrome.
Status | Completed |
Enrollment | 46 |
Est. completion date | July 2017 |
Est. primary completion date | July 2017 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 75 Years |
Eligibility |
Inclusion Criteria: - Patients between 18 and 75 years old with diagnosis of subacromial impingement syndrome or any of the pathologies that compose it (tendinosis-tendinitis supraspinatus and rest of the rotator cuff, subacromial bursitis and tendinitis of the long head of the biceps). - Visual Analogue Scale (VAS) less than or equal to 7. - Forward flexion at least of 100º Exclusion Criteria: - Calcific tendinitis - Complete rupture of the rotator cuff. - Adhesive capsulitis. - Clinical history of pathologies that without affecting the shoulder joint refer to painful shoulder symptoms (cervical root involvement, cervical surgery, cervical osteoarthritis and neurological pathologies) - Fibromyalgia - Be receiving physiotherapeutic treatment or have received it previously for this pathology one month before the start of treatment. - Patients with alterations of thermal sensitivity. - Derived from the absolute and relative contraindications of Laser Therapy: - Photosensitive patients - Neoplastic processes - Hyperthyroidism - Pregnancy - Patients with a history of epileptic seizures |
Country | Name | City | State |
---|---|---|---|
Spain | Hospital General Nuestra Señora del Prado | Talavera de la Reina | Toledo |
Lead Sponsor | Collaborator |
---|---|
University of Castilla-La Mancha | Castilla-La Mancha Health Service, Hospital General Nuestra Señora del Prado |
Spain,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Quality of life | EQ-5D™ is a standardised instrument for use as a measure of health outcome. | Baseline | |
Primary | Shoulder Pain and Disability Index (SPADI) | SPADI test | Baseline | |
Primary | Shoulder Pain and Disability Index (SPADI) | SPADI test | At the end of the laser protocol treatment (1 daily session during 15 workday -from monday to friday-) | |
Primary | Shoulder Pain and Disability Index (SPADI) | SPADI test | one month after the end of the protocol treatment | |
Primary | Shoulder Pain and Disability Index (SPADI) | SPADI test | three months after the end of the protocol treatment | |
Primary | Constant-Murley Score | Constant-Murley Score without strength section. The results will be expressed on a maximum of 75 points. | Baseline | |
Primary | Constant-Murley Score | Constant-Murley Score without strength section. The results will be expressed on a maximum of 75 points. | At the end of the laser protocol treatment (1 daily session during 15 workday -from monday to friday-) | |
Primary | Constant-Murley Score | Constant-Murley Score without strength section. The results will be expressed on a maximum of 75 points. | one month after the end of the protocol treatment | |
Primary | Constant-Murley Score | Constant-Murley Score without strength section. The results will be expressed on a maximum of 75 points. | three months after the end of the protocol treatment | |
Primary | Quick-Dash Abbreviated | Quick- Dash Abbreviated test | Baseline | |
Primary | Quick-Dash Abbreviated | Quick- Dash Abbreviated test | At the end of the laser protocol treatment (1 daily session during 15 workday -from monday to friday-) | |
Primary | Quick-Dash Abbreviated | Quick- Dash Abbreviated test | one month after the end of the protocol treatment | |
Primary | Quick-Dash Abbreviated | Quick- Dash Abbreviated test | three months after the end of the protocol treatment | |
Secondary | Painful pressure threshold | The pressure pain threshold will be measured by a pressure algometer and will be expressed in Newton. | Baseline, at the of the 15 sessions, one month after the end of the protocol treatment, three months after the end of the protocol treatment | |
Secondary | Painful pressure threshold after first session | The pressure pain threshold will be measured by a pressure algometer and will be expressed in Newton. | First session - 15 minutes after laser or sham treatment. | |
Secondary | VAS | Visual analogue scale | Baseline, at the of the 15 sessions, one month after the end of the protocol treatment, three months after the end of the protocol treatment |
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