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Background: Ankylosing spondylitis imposes burdens on individuals and society that AS costs 3 times higher than general population. Conventional approaches for AS have their limitation. Previous studies demonstrated acupuncture has significant therapeutic effects for AS in diminishing joint pain, enhancing functional disorders and modifying spinal deformity. Although acupuncture is effective in relieving pain in AS patients, the evidence is very limited due to methodological flaws.
Design This study will be a single-arm pilot study in patients with AS. Eligible subjects will receive electroacupuncture treatment twice per week for at least 6 weeks (12 sessions in total). The length of treatment can be extended to a maximum of 10 weeks (20 sessions in total) if participants request a prolonged treatment. The acupuncturist, who is a registered Chinese medicine practitioner, of this trial will not participate in data collection and data entry.
Objective: To explore the treatment effect of electroacupuncture for relieving pain in ankylosing spondylitis.
Setting: Hong Kong
Participants: 20 subjects with a diagnosis of ankylosing spondylitis
Main Measures: Pain Severity Numerical Rating Scale (NRS), Adverse events
Data analysis All data will be double-entered and checked for consistency before conducting the analysis. Binomial test will be used to analyze the percentage of responders to treatment compared with a reference value of 10%. Wilcoxon signed rank test will be used to compare the values of all continuous variables between baseline and post treatment. The population for safety analyses will include all subjects who receive at least one acupuncture treatment. Adverse events will be coded using the WHO Adverse Reaction Terminology Dictionary. Special attention will be given to those subjects who have discontinued treatment due to adverse events or who experience serious adverse events.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Electroacupuncture | Experimental |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Electroacupuncture | Device |
|
| Measure | Description | Time Frame |
|---|---|---|
| Change in Pain Severity Numerical Rating Scale (NRS) | week 0 and 6 |
| Measure | Description | Time Frame |
|---|---|---|
| Types and dosage of drug(s) intake | week 0, 2, 4, 6, 8, 10, 12, 14 and 18 | |
| Bath Ankylosing Spondylitis Functional Index (BASFI) | week 0, 6, 10 and 18 | |
| Bath Ankylosing Spondylitis Disease Activity Index (BASDAI) |
| Measure | Description | Time Frame |
|---|---|---|
| Number of patients withdraw and the corresponding reasons | 18 weeks | |
| Number of subjects with and corresponding types of adverse events | 18 weeks | |
| Treatment Credibility by the Credibility of Treatment Rating Scale (CTRS) |
Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Lixing LAO, Ph.D. | The University of Hong Kong | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| The University of Hong Kong | Hong Kong | Hong Kong |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 42179340 | Derived | Lam WL, Yeung WF, Lau CS, Jiang F, Chen H, Lao L. Electroacupuncture for the relief of suboptimally managed pain in ankylosing spondylitis: A single-arm pilot study. Acupunct Med. 2026 May 25:9645284261444761. doi: 10.1177/09645284261444761. Online ahead of print. |
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| ID | Term |
|---|---|
| D013167 | Spondylitis, Ankylosing |
| ID | Term |
|---|---|
| D000089183 | Axial Spondyloarthritis |
| D025242 | Spondylarthropathies |
| D025241 | Spondylarthritis |
| D013166 | Spondylitis |
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| ID | Term |
|---|---|
| D015671 | Electroacupuncture |
| ID | Term |
|---|---|
| D003131 | Combined Modality Therapy |
| D013812 | Therapeutics |
| D015670 | Acupuncture Therapy |
| D000529 | Complementary Therapies |
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| week 0, 6, 10 and 18 |
| Bath Ankylosing Spondylitis Global Index (BASGI) | week 0, 6, 10 and 18 |
| Quality of life of patients as evaluated by SF-36 | Quality of life of patients will be measured. | week 0, 6, 10 and 18 |
| Bath Ankylosing spondylitis Metrology Index (BASMI) | week 0, 6, 10 and 18 |
| Chest expansion as measured by the change in circumference at 4th intercostal level between maximal inspiration and expiration in cm | week 0, 6, 10 and 18 |
| Joints count | week 0, 6, 10 and 18 |
| C-reactive protein (CRP) | week 0, 6, 10 and 18 |
| Erythrocyte sedimentation rate (ESR) | week 0, 6, 10 and 18 |
| Change in Pain Severity Numerical Rating Scale (NRS) | week 0, 2, 4, 8, 10, 12, 14, and 18 |
| Week 0,6 and 10 |
| D013122 |
| Spinal Diseases |
| D001847 | Bone Diseases |
| D009140 | Musculoskeletal Diseases |
| D000844 | Ankylosis |
| D007592 | Joint Diseases |
| D001168 | Arthritis |
| D004599 |
| Electric Stimulation Therapy |
| D026741 | Physical Therapy Modalities |
| D012046 | Rehabilitation |
| D004561 | Transcutaneous Electric Nerve Stimulation |
| D000698 | Analgesia |
| D000760 | Anesthesia and Analgesia |
| D000758 | Anesthesia |