Influence of Interferential Current Therapy in the Treatment of Individuals With Shoulder Impact Syndrome: A Randomized, Placebo Controlled Clinical Trial.

NCT ID: NCT02964819

Last Updated: 2017-01-18

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 45 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2016-01-31
• Study Completion Date: 2016-12-31

Brief Summary

This project will analyze the influence of interferential current therapy in an exercise program for individuals with a unilateral impact syndrome diagnosis. To that end, volunteers of both genders, aged 18-59 years, had an unilateral, unilateral pain in the shoulder with more than 3 months duration, at least grade 4 pain by the numerical scale of pain assessment, positivity In at least 2 of 3 orthopedic tests for impact syndrome, will be randomized into the following groups: exercise group, exercise + ultrasound group, exercise group + interferential current. Sixteen consecutive treatment sessions will be performed, and the volunteers will be evaluated before and after, by means of the following instruments: Numerical scale of evaluation of pain, Shoulder pain and disability index (SPADI), Pain-Related Catastrophizing Thoughts Scale, being applied the Numerical scale of evaluation of pain at the end of Each session and one month after the end of treatment.

Conditions

Shoulder Impingement Syndrome

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: DOUBLE

Study Groups

exercise group

Manual cervical traction, Myofascial release of upper trapezius muscle, 3 sets of 1 minute;Sleeper's stretch, during 3 series of 30 seconds,Punch exercise, Knee push-up plus, Prone V-raise exercise (arms abducted at 120°), rotador cuff exercise (internal rotation), rotador cuff exercise (external rotation), Rotation on the wall using a ball (internal rotation), Rotation on the wall using a ball (external rotation).

Group Type: ACTIVE_COMPARATOR

exercise

Intervention Type: OTHER

exercise + Interferential current group

Addition to the exercise protocol performed in the exercise group the interferential current. Four self-adhesive electrodes (8x5 cm), two upper and two lower ones (forming a square) will be placed around the center of the shoulder. The electrodes will be positioned crosswise, following the parameters: 4KHz (carrier frequency), 1/1 second (swing pattern), 100 Hz Frequency modulation amplitude (AMF), 50 Hz (sweep frequency), automatic vector mode, With intensity at the motor threshold of sensation, with duration of 50 minutes.

Group Type: EXPERIMENTAL

exercise

Intervention Type: OTHER

Interferential current therapy

Intervention Type: DEVICE

exercise + US group

In addition to the exercise protocol performed in the exercise group, an ultrasound device will be used. The appliance will be used off, without any individual participant having knowledge. For this, the individual will be asked to position himself in the dorsal position on the stretcher, the therapist will perform the application of the transducer head, with gel on its surface, in the anterolateral region of the affected shoulder.

Group Type: PLACEBO_COMPARATOR

exercise

Intervention Type: OTHER

Therapeutic Ultrasound

Intervention Type: DEVICE

Interventions

exercise

Intervention Type: OTHER

Interferential current therapy

Intervention Type: DEVICE

Therapeutic Ultrasound

Intervention Type: DEVICE

Eligibility Criteria

Inclusion Criteria

• History of anterolateral, unilateral pain in the shoulder with more than 3 months duration.
• Medical diagnosis,
• minimal grade 4 pain by numerical scale of pain assessment,
• positivity in at least 2 of 3 orthopedic tests for impact syndrome: Neer, Hawkins or Jobe.

Exclusion Criteria

• Fibromyalgia diagnosis,
• pregnancy,
• numbness or tingling in the upper limb
• History of shoulder trauma, other shoulder related diseases,
• ruptured tendons, ligament laxity,
• symptoms of numbness and / or Tingling in the upper limbs, history of shoulder and / or cervical surgery
• use of corticosteroid injection in the shoulder, and analgesic, anti-inflammatory or muscle relaxant use and have or have undergone physiotherapeutic treatment in the last 6 months.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 59 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

University of Nove de Julho

OTHER

Sponsor Role: lead

Responsible Party

Cid André Fidelis de Paula Gomes

Professor

Responsibility Role: PRINCIPAL_INVESTIGATOR

Locations

University of Nove de Julho

São Paulo, São Paulo, Brazil

Countries

Brazil

Other Identifiers

51675615.3.0000.5511

Identifier Type: -

Identifier Source: org_study_id