Skip to content

Shoulder pain: To needle or not to needle? The role of acupuncture in the treatment of shoulder pain

A multicentre randomised trial comparing exercise, acupuncture and electro-acupuncture for people with shoulder pain

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN10708719
Enrollment
234
Registered
2015-07-27
Start date
2007-07-31
Completion date
Unknown
Last updated
2018-01-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Shoulder pain of musculoskeletal origin Musculoskeletal Diseases Shoulder pain

Interventions

Group 1: Shoulder exercise group Group 2: Shoulder exercise group and acupuncture Group 3: Shoulder exercise group and electro-acupuncture

Sponsors

Chelsea and Westminster Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patients referred to physiotherapy departments who have pain in the region of their shoulder 2. Minimum duration of symptoms being 3 months 2. Being able fully communicate in English 3. A minimum age of 18 years

Exclusion criteria

Exclusion criteria: 1. Pain referred from the cervical spine 2. A history of shoulder instability, subluxations, dislocations 3. Un-united fractures involving the shoulder 4. Malunion or non-union of fractures 5. Inability to participate in an exercise programme 6. Systemic diseases such as rheumatoid arthritis, diabetes, uncontrolled blood pressure, cardiac disease, renal insufficiency, cardiac pacemakers, hearing aids 7. Women who are pregnant, attempting to become pregnant 8. Fear of needles (participants may be randomised to a group where acupuncture needles will be used). 9. Infections (systemic or local) 10. Fragile, swollen, thin or inflamed skin 11. Post-surgical lymphoedema 12. Known allergy to metals 13. Recent oral steroid therapy or shoulder injections 14. Epilepsy 15. Patients on anti-coagulation therapy 16. Patients with Hemophilia

Design outcomes

Primary

MeasureTime frame
1. Oxford Shoulder Score (a validated 12 question questionnaire which requires tick box responses relating to the patients symptoms and level of disability) Outcome measurements will be taken (1) before the commencement of the programme, (2) immediately after the programme, (3) at 6 months and (4) at 12 months.

Secondary

MeasureTime frame
1. Shoulder Pain and Disability Index (SPADI), another validated shoulder questionnaire which also includes Visual Analogue Scales for pain 2. Shoulder range of movement (shoulder flexion, abduction, external rotation and internal rotation) measured with goniometers and tape measurer 3. Shoulder strength measured with a validated shoulder strength testing dynanometer. 4. Global impression of change Outcome measurements will be taken (1) before the commencement of the programme, (2) immediately after the programme, (3) at 6 months and (4) at 12 months.

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026