Effectiveness of Physiotherapy for Chronic Shoulder Pain

University of Melbourne120 enrolled

Overview

The purpose of this study is to investigate whether a physiotherapy program reduces pain and improves disability and quality-of-life in people with chronic shoulder pain. The main study hypotheses are that (i) A 10-week physiotherapy treatment will result in significantly greater reductions in pain and disability than placebo treatment in individuals with chronic shoulder pain (ii) Improvements in pain and disability following a 10-week physiotherapy treatment will be maintained at a 3-month follow-up.

Chronic rotator cuff pathology (CRCP) is a common cause of musculoskeletal morbidity in the community. Physiotherapy is often the first line of management for this condition. However, the effectiveness of physiotherapy for CRCP has not been well studied. Thus this project primarily aims to investigate the effect of a multimodality physiotherapy program to treat CRCP where effect is measured in terms of pain, disability and health-related quality of life. The secondary aim is to evaluate the cost-effectiveness of physiotherapy as a treatment for CRCP. Comparison: physiotherapy program comprising stretches, exercises, manual techniques versus placebo physiotherapy

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

DOUBLE

Enrollment

120

Conditions

Shoulder Pain

Interventions

Physiotherapy programPROCEDURE

Placebo physiotherapy treatmentPROCEDURE

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: * diagnosis of CRCP as evident by symptoms and signs including pain on active abduction or external rotation and positive impingement test; * symptoms of pain in shoulder for \> 3 months; * average movement pain \> 3 on a 10 cm visual analogue scale; * aged ≥ 18 years; * able to understand written and spoken English. Exclusion Criteria: * severe pain at rest, defined as \> 7 on a visual analogue scale; * global restriction of shoulder movements; * systemic inflammatory joint disease; * x-ray evidence of shoulder osteoarthritis or fracture; * calcification about the shoulder joint; * reason to suspect a complete rotator cuff rupture (eg. weakness of arm elevation, a positive "drop arm sign", a high riding humerus visible on x-ray or a complete tear on ultrasound); * previous shoulder surgery on affected arm; * physiotherapy, corticosteroid injection or hydrodilatation for shoulder in past 3 months; * commenced non-steroidal antiinflammatory medication (NSAIDs) or conservative intervention in past 2 weeks.

Locations (1)

University of Melbourne

Melbourne, Victoria, Australia

Outcomes

Primary Outcomes

Shoulder Pain and Disability Index

Time frame: Baseline and 11 weeks

Participant perceived global rating of change post treatment

Time frame: 11 weeks

Secondary Outcomes

Shoulder Pain and Disability Index at followup

Time frame: 22 weeks

Participant perceived global rating of change at followup

Time frame: 22 weeks

Australian Quality of Life Index at followup

Time frame: Baseline, 11 weeks and 22 weeks

Isometric Shoulder strength using manual muscle tester post treatment and followup

Time frame: Baseline, 11 weeks and 22 weeks

Participant assessment of average pain and restriction of activity post treatment and followup

Time frame: Baseline, 11 weeks and 22 weeks

Cost effectiveness analysis

Time frame: Baseline, 11 weeks and 22 weeks

Data from ClinicalTrials.gov

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