RecruitingNot ApplicableNCT05951933

Transcranial Electrical Stimulation in Subacromial Pain Syndrome

Effectiveness of Transcranial Electrical Stimulation in the Functional Recovery of Subjects with Subacromial Pain Syndrome: Randomized Clinical Trial.


Sponsor

University of Valencia

Enrollment

74 participants

Start Date

Nov 23, 2023

Study Type

INTERVENTIONAL

Conditions

Summary

The goal of this clinical trial is to analyze whether a physiotherapy protocol based on strengthening exercises to the shoulder girdle muscles carried on during anodal transcranial electrical stimulation (a-TES) is more effective on the symptoms and functionality of subjects with subacromial pain syndrome than an isolated strengthening program. The main questions it aims to answer are: * Is the strengthening + a-TES protocol effective on functionality? * Is the strengthening + a-TES protocol effective on quality of life? * Is the strengthening + a-TES protocol effective on pain? * Is the strengthening + a-TES protocol effective on muscle strength? * Is the strengthening + a-TES protocol effective on active range of movement? * Is the strengthening + a-TES protocol effective on proprioception? * Is the strengthening + a-TES protocol effective on posture? * Is the strengthening + a-TES protocol effective on glenohumeral and scapulothoracic kinematics? Participants will perform an 8 weeks-3 days/week shoulder strengthening protocol for the rotator cuff and scapulothoracic muscles using elastic bands and dumbbells. The rotator cuff exercises will be performed while they receive a-TES using a neoprene helmet with the electrodes placed in the opposite hemisphere to the affected side. The scapulothoracic exercises will be performed without the transcranial stimulation. The experimental group will receive real a-TES, and will be compared with a control group that will perform the same therapeutic exercises but with placebo a-TES to see the effectiveness of the a-TES on the outcomes cited above.


Eligibility

Min Age: 18 YearsMax Age: 65 Years

Inclusion Criteria9

  • Subjects will be evaluated during a first consultation by a physiotherapist with experience in shoulder musculoskeletal pathology, following the algorithm for the diagnosis of shoulder problems, recommended by the British Elbow \& Shoulder Society with the aim of detecting possible "flags red" and as a guide to rule out other shoulder pathologies that do not fit into the SDS. However, other tests will be added to ensure diagnostic accuracy, and these are described below.
  • Age between 18 and 65 years.
  • Duration of pain greater than or equal to 3 months.
  • Presence of 3 or more of the following positive clinical tests:
  • painful arc
  • External rotation test against isometric resistance
  • Neer's test
  • Jobe test or empty can test
  • Hawkins-Kennedy test

Exclusion Criteria22

  • Previous shoulder or neck surgery.
  • History of shoulder fracture or dislocation.
  • Medical diagnosis of shoulder osteoarthritis.
  • Adhesive capsulitis
  • Cervicobrachialgia or reproducible shoulder pain with neck movements.
  • Clinical signs of total tear of the rotator cuff.
  • Corticosteroid injection in the previous 6 weeks.
  • Inflammatory disease, autoimmune or rheumatic, systemic (arthritis, lupus, myopathies).
  • Cognitive or behavioral problems that make it impossible to understand and follow the intervention (score less than 24 on the Mini-Mental State Examination Score) (73).
  • Any neurological or neoplastic disease.
  • Also those who present contraindications for transcranial electrical stimulation. For this, the recommendations of the checklist of Thair et al. which includes:
  • personal and family history of epilepsy
  • metal implants in the head
  • implanted medication pump
  • pacemaker
  • recurring headaches
  • skin diseases of the scalp (psoriasis, eczema)
  • head injuries
  • serious head surgeries
  • pregnancy
  • heart diseases
  • medications (psychotropics or antihistamines).

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Interventions

OTHERStrenghtening + TES

Strenghtening of rotator cuff and scapulothoracic muscles protocol with the incorporation of anodal transcranial direct stimulation (real if experimental or sham if control)


Locations(1)

University of Valencia

Valencia, Valencia, Spain

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NCT05951933


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