Working…
COVID-19 is an emerging, rapidly evolving situation.
Get the latest public health information from CDC: https://www.coronavirus.gov.

Get the latest research information from NIH: https://www.nih.gov/coronavirus.
ClinicalTrials.gov
ClinicalTrials.gov Menu

Efficacy of Neuromuscular Bandage Technique Against Jones Technique After the Supraespinatus Muscle Tendon Suture

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT02812381
Recruitment Status : Completed
First Posted : June 24, 2016
Last Update Posted : August 31, 2016
Sponsor:
Information provided by (Responsible Party):
Fundacion para la Investigacion Biomedica del Hospital Universitario Ramon y Cajal

Brief Summary:

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

Detailed Description:

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.

Layout table for study information
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)




Primary Outcome Measures :
  1. 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,


Secondary Outcome Measures :
  1. 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


Other Outcome Measures:
  1. 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



Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Layout table for eligibility information
Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

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 .

Information from the National Library of Medicine

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


Sponsors and Collaborators
Fundacion para la Investigacion Biomedica del Hospital Universitario Ramon y Cajal
Investigators
Layout table for investigator information
Principal Investigator: ANA ROMOJARO, THERAPIST UNIVERSIDAD DE ALCALA
Layout table for additonal information
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"
Keywords provided by Fundacion para la Investigacion Biomedica del Hospital Universitario Ramon y Cajal:
Trigger Points, movement