Clinical Trial of Electroacupuncture in Axial Spondyloarthritis (E-AcuSpA)

N/AUnknownNCT04519866

Singapore General Hospital100 enrolled

Overview

Axial spondyloarthritis (AxSpA) is a chronic disease that causes severe disability and poor quality of life. Current treatment options are limited and there are still significant non-responders to current western medications. Manual acupuncture has been shown to reduce pain in patients with AxSpA. There have been reports of electroacupuncture demonstrating more sustained pain relief. Therefore, the investigators aim to determine the clinical effectiveness, safety and cost-effectiveness of electroacupuncture as compared to manual acupuncture for patients with AxSpA through a randomized controlled trial.

Patients with active axial spondyloarthritis despite non-steroidal anti-inflammatory drugs (NSAIDs) or biologics, will be randomly allocated to receive electroacupuncture or manual acupuncture on a 1:1 basis via random permuted block randomization. All patients will receive their standard of care (drug therapy and physiotherapy) as background therapy. This study will not be investigating any therapeutic or medicinal products (drugs). Primary outcome would be the mean difference in Bath Ankylosing Spondylitis Disease Activity Index (BASDAI) score between the 2 groups over 12 weeks (as assessed at weeks 0, 3, 6, 9, 12) adjusted for baseline covariate and other potential confounders. Patients will be followed up for BASDAI, other clinical, quality of life (QoL), economic outcomes as well as Traditional Chinese Medicine (TCM) syndrome scores over time for secondary and exploratory outcomes. A cost-effectiveness analysis will be performed. Adverse events will be recorded. The primary hypothesis is that electroacupuncture may result in better disease activity control in patients with AxSpA as compared to manual acupuncture over 12 weeks, while secondary hypothesis is that electroacupuncture may result in greater improvements in other clinical and quality of life outcomes as compared to those receiving manual acupuncture over 24 weeks. The investigators also hypothesize that there is no difference in safety between both arms.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

Interventions

ElectroacupunctureOTHER

Manual acupuncture (see procedures below) will be administered first to obtain the "de qi" sensation. After "de qi" is obtained, the electroacupuncture unit will be connected to 1-3 pairs of acupoints. Current intensity used will be based on the tolerance of each patient. Needles with electrical stimulation will be retained for 30 min. Main acupoints will be Jingjin points (meridian sinews) along the Bladder meridian of Foot - Taiyang, such as Shenshuci, as well as Jingjin points (meridian sinews) at transverse process from L2 to L4, iliac crest and spinous process from S1 to S4. Secondary acupoints will also be selected based on patients' syndromes and symptoms.

Manual acupunctureOTHER

After disinfecting the acupuncture points, acupuncture will be performed with the patient lying prone. Depending on the acupuncture points, 0.25mm X 25-75 mm sterile acupuncture needle will be used. Needles will be inserted 10-50 mm and either rotating manipulation or lifting-thrusting manipulation will be used to achieve "de qi" (a compositional sensation including soreness, numbness, distention and heaviness). Acupoints used will be similar to those mentioned for electroacupuncture (see above).

Eligibility

Sex: ALLMin age: 21 YearsMax age: 100 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Aged 21 years of age or older * Diagnosed with AxSpA according to the 2009 Assessment of Spondyloarthritis International Society (ASAS) criteria * Bath AS Disease Activity Index (BASDAI) score ≥4 on a 11-point Numerical Rating Scale (NRS) * Failed 2 sequential NSAIDs (including cyclooxygenase-2 inhibitor) at maximal tolerated doses for ≥4 weeks in total * Patients on concomitant biological therapy (e.g. tumour necrosis factor inhibitor therapy, anti-interleukin 17) or non-biologic disease-modifying antirheumatic drugs (DMARDs) (e.g. methotrexate (MTX) or sulfasalazine (SSZ) or leflunomide (LEF)) at study entry must be on the drug for ≥12 weeks and at stable dose for ≥4 weeks prior to randomisation * Patients taking systemic corticosteroids have to be on stable dose of ≤10mg/day prednisolone or equivalent for at least two weeks before randomisation. Exclusion Criteria: * Pregnant or breastfeeding women * With bleeding disorders * With blood-borne communicable diseases (e.g. hepatitis B, hepatitis C, human immunodeficiency virus, etc) * With implantable electrical device (e.g. pacemaker) * Suffering from impaired skin sensation or serious skin lesions along the vertebrae

Outcomes

Primary Outcomes

Mean difference in Bath Ankylosing Spondylitis Disease Activity Index (BASDAI) score between both groups

Mean difference in BASDAI score between both groups from baseline to weeks 3, 6, 9 and 12. BASDAI score ranges from 0-10, with higher scores indicating higher disease activity.

Time frame: Week 3, 6, 9, 12

Secondary Outcomes

Mean difference in Bath Ankylosing Spondylitis Functional Index (BASFI) score between both groups

Mean difference in BASFI score between both groups from baseline to weeks 6, 12 and 24. BASFI score ranges from 0-10, with higher scores indicating poorer functioning.

Time frame: Week 6, 12, 24

Mean difference in Bath Ankylosing Spondylitis Patient Global score (BAS-G) between both groups

Mean difference in BAS-G score between both groups from baseline to weeks 6, 12 and 24. BAS-G score ranges from 0-10, with higher scores reflecting poorer well-being.

Time frame: Week 6, 12, 24

Mean difference in Assessment of Spondyloarthritis International Society Health Index (ASAS HI) score between both groups

Mean difference in ASAS HI score between both groups from baseline to weeks 6, 12 and 24. ASAS HI score ranges from 0-17, with higher scores indicating poorer health status.

Time frame: Week 6, 12, 24

Mean difference in Ankylosing Spondylitis Quality of Life (ASQoL) score between both groups

Mean difference in ASQoL score between both groups from baseline to weeks 6, 12 and 24. ASQoL score ranges from 0-18, with higher scores indicating worse quality of life.

Time frame: Week 6, 12, 24

Mean difference in EuroQol- 5 Dimension (EQ-5D) score between both groups

Mean difference in EQ-5D score between both groups from baseline to weeks 6, 12 and 24. EQ-5D consists of a descriptive system and a visual analogue scale. The descriptive system covers 5 dimensions: mobility, self-care, usual activities, pain/ discomfort and anxiety/ depression. Each dimension has a minimum and maximum score of 1 and 5 respectively, with higher scores representing a greater problem in that dimension. The visual analogue scale ranges from 0-100, with lower scores indicating poorer health status.

Time frame: Week 6, 12, 24

Mean difference in Work Productivity and Activity Impairment (WPAI) score between both groups

Mean difference in WPAI score between both groups from baseline to weeks 6, 12 and 24. WPAI measures absenteeism, presenteeism, work productivity loss and activity impairment. These are expressed as percentages, from 0-100, with higher numbers indicating greater impairment and less productivity.

Time frame: Week 6, 12, 24

Mean difference in healthcare costs between both groups

Mean difference in healthcare costs will be assessed for both groups at weeks 6, 12 and 24.

Time frame: Week 6, 12, 24

Mean difference in Bath Ankylosing Spondylitis Disease Activity Index (BASDAI) score between both groups

Mean difference in BASDAI score between both groups from baseline to week 24. BASDAI score ranges from 0-10, with higher scores indicating higher disease activity.

Time frame: Week 24

Clinical Trial of Electroacupuncture in Axial Spondyloarthritis (E-AcuSpA)

Overview

Conditions

Interventions

Eligibility

Locations (1)

Outcomes

Primary Outcomes

Secondary Outcomes

Central Contacts