Efficacy of Neuromuscular Bandage Technique Against Jones Technique After the Supraespinatus Muscle Tendon Suture
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ClinicalTrials.gov Identifier: NCT02812381 |
Recruitment Status :
Completed
First Posted : June 24, 2016
Last Update Posted : August 31, 2016
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The suture of the supraspinatus tendon is a common surgery that requires physical therapy for back pain and functional impairment to such surgery. Kinesiotaping technique (KT) is being used to treat myofascial trigger points that appear after surgery and for the treatment of physiotherapy in the supraspinatus muscle and deltoid.
To evaluate the effectiveness of KT technique over the technique of Jones (Straincounterstrain or SCS) in patients undergoing suture the tendon of the supraspinatus muscle.
Condition or disease | Intervention/treatment | Phase |
---|---|---|
Pain | Procedure: KT Procedure: SCS | Not Applicable |
Objective: To evaluate the effectiveness of the KT technique against Jones (Strain-Counterstrain or SCS) technique in patients with the suture of the tendon of the supraspinatus muscle.
Design: Test clinically controlled, randomized, masking of intervention by double placebo and blind to the subject of the essay and the Studio analyst.
METHOD: Patients with supraspinatus tendon suture are randomly divided into two groups: a group treated with KT (n = 18) and other treated with SCS (n = 18). The treatment was applied the 1st, 4th and 8th day of physical therapy session. All patients were evaluated the 1st and the 12th day of the session with the visual analog scale of pain (VAS), with the scale of Disabilities of the arm, shoulder and hand (DASH) to assess the functionality and active direction-finding (ROM) to assess travel articulate.
Study Type : | Interventional (Clinical Trial) |
Actual Enrollment : | 36 participants |
Allocation: | Randomized |
Intervention Model: | Parallel Assignment |
Masking: | Single (Participant) |
Primary Purpose: | Treatment |
Official Title: | Efficacy of Neuromuscular Bandage Technique Against Jones Technique After the Supraespinatus Muscle Tendon Suture: a Prospective Randomized Clinical Trial |
Study Start Date : | July 2016 |
Actual Primary Completion Date : | July 2016 |
Actual Study Completion Date : | August 2016 |
Arm | Intervention/treatment |
---|---|
Active Comparator: SCS (Jones tecnique)
18 patients were treatment with straincounterstrain
|
Procedure: SCS
To aplicate strain-counterstrain above trigger point |
Sham Comparator: KT Kinesiotaping
18 patients were treatment with neuromuscular bandage
|
Procedure: KT
to aplicate neuromuscular bandage technique(KT) |
- Change in the DASH between sixth and eighth week , in patients with supraespinatus muscle tendon suture. [ Time Frame: From first day of the sixth week after surgery to twelve days after of the first medition. ]
All participants (36) has been mesured:
- First day of the sixth week after surgery with DASH,
- Four days later of the first medition , it repeated the technique asigned but it hasn´t been mesured.
- Eight days later or the first meditión, it repeated the technique asigned but it hasn´t been mesured.
- Twelve days later of the first medition , it repeated the mesured with DASH,
- Change in the VAS between sixth and eighth week , in patients with supraespinatus muscle tendon suture. [ Time Frame: From first day of the sixth week after surgery to twelve days after of the first medition. ]
All participants (36) has been mesured:
- First day of the sixth week after surgery with VAS scale.
- Four days later of the first medition , it repeated the technique asigned but it hasn´t been mesured.
- Eight days later or the first meditión, it repeated the technique asigned but it hasn´t been mesured.
- Twelve days later of the first medition , it repeated the mesured with VAS
- Change in the ROM between sixth and eighth week , in patients with supraespinatus muscle tendon suture. [ Time Frame: From first day of the sixth week after surgery to twelve days after of the first medition. ]
All participants (36) has been mesured:
- First day of the sixth week after surgery with ROM
- Four days later of the first medition , it repeated the technique asigned but it hasn´t been mesured.
- Eight days later or the first meditión, it repeated the technique asigned but it hasn´t been mesured.
- Twelve days later of the first medition , it repeated the mesured with ROM

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Ages Eligible for Study: | 18 Years and older (Adult, Older Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
- Among patients attending the 1st and 5th week after Intervention.
- Patients with age above 18 years.
- Patients of both sexes.
- Patients with a detectable with algometer trigger point in the supraspinatus and / or deltoid .
Exclusion Criteria:
- Patient with Impaired Communication .
- Patients with signs of infection .
- Patients with previous surgery on the shoulder or shoulder capsulitis submit .
- Patient scammers cervical herniated discs or brachial neuropathy .
- Patients with tumor pathology.
- Patients with fibromyalgia,
- Pregnant patients.
- Patients with central pain .
- Patients conducted simultaneously treatments .

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02812381
Principal Investigator: | ANA ROMOJARO, THERAPIST | UNIVERSIDAD DE ALCALA |
Responsible Party: | Fundacion para la Investigacion Biomedica del Hospital Universitario Ramon y Cajal |
ClinicalTrials.gov Identifier: | NCT02812381 |
Other Study ID Numbers: |
BC-2013 |
First Posted: | June 24, 2016 Key Record Dates |
Last Update Posted: | August 31, 2016 |
Last Verified: | March 2016 |
Individual Participant Data (IPD) Sharing Statement: | |
Plan to Share IPD: | Yes |
Plan Description: | The investigators would like to share in the magazine "Manual Therapy" |
Trigger Points, movement |