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

NCT ID: NCT02812381

Last Updated: 2016-08-31

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

36 participants

Study Classification

INTERVENTIONAL

Study Start Date

2016-07-31

Study Completion Date

2016-08-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

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.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

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.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Pain

Keywords

Explore important study keywords that can help with search, categorization, and topic discovery.

Trigger Points, movement

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Participants

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

SCS (Jones tecnique)

18 patients were treatment with straincounterstrain

Group Type ACTIVE_COMPARATOR

SCS

Intervention Type PROCEDURE

To aplicate strain-counterstrain above trigger point

KT Kinesiotaping

18 patients were treatment with neuromuscular bandage

Group Type SHAM_COMPARATOR

KT

Intervention Type PROCEDURE

to aplicate neuromuscular bandage technique(KT)

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

KT

to aplicate neuromuscular bandage technique(KT)

Intervention Type PROCEDURE

SCS

To aplicate strain-counterstrain above trigger point

Intervention Type PROCEDURE

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

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 .
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Fundacion para la Investigacion Biomedica del Hospital Universitario Ramon y Cajal

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

ANA ROMOJARO, THERAPIST

Role: PRINCIPAL_INVESTIGATOR

UNIVERSIDAD DE ALCALA

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

BC-2013

Identifier Type: -

Identifier Source: org_study_id