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The Clinical Efficacy of Belting Stabilization for Shoulder Pain

S

Sunnybrook Health Sciences Centre

Status and phase

Completed
Phase 1

Conditions

Rotator Cuff Impingement Syndrome

Treatments

Procedure: Stabilization belt

Study type

Interventional

Funder types

Other

Identifiers

NCT00826293
224-2008

Details and patient eligibility

About

Application of a belt for stabilization while exercising accelerate and optimize recovery in patients diagnosed with shoulder impingement syndrome.

Full description

Stabilization through belts is commonly used as an adjunct for treatment of musculoskeletal problems. Although this treatment is popular among clinicians, there is a paucity of evidence on its use for shoulder pathology. The objective of this double-blinded longitudinal randomized controlled trial (RCT) is to determine the clinical efficacy of stabilization belting applied to patients receiving rehabilitation treatment for shoulder impingement syndrome. The study population will include patients who have been referred to the physiotherapy department of the Holland Orthopaedic & Arthritic Centre for conservative treatment. Patients will be randomized into the treatment and control groups. The primary outcome measure is the Quick Disabilities of Arm, Shoulder and Hand (QuickDASH) questionnaire.

Enrollment

64 patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Diagnosis of impingement syndrome or post-surgical stiffness with an abnormal scapulothoracic rhythm

Exclusion criteria

  • Inability to speak or read English
  • Evidence of major joint trauma causing fracture
  • Infection
  • Underlying metabolic or inflammatory disease
  • Avascular necrosis
  • Frozen shoulder
  • Major medical illness
  • Psychiatric illness that precluded informed consent

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

64 participants in 2 patient groups

True Stabilization Group
Active Comparator group
Description:
Patients will be randomized to one of the two treatment groups (true stabilization vs. sham stabilization). Patients will be exercising with a belt that is expected to reduce impingement of the rotator cuff tendons.
Treatment:
Procedure: Stabilization belt
Procedure: Stabilization belt
Sham Stabilization
Sham Comparator group
Description:
Patients receive sham stabilization. The sham procedure imitates the treatment without any true effect.
Treatment:
Procedure: Stabilization belt
Procedure: Stabilization belt

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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