The protocol of this study was published in detail during the trial[17]
Study design and participants
We designed a single-centre, three-armed, randomized, double-blind, controlled trial. Patients with a documented UESPAS were allocated and randomly assigned to three groups (a control group, a Filiform-needle acupuncture group and FFN acupuncture group) through central randomization in a 1:1:1 ratio. This trial was approved by the Ethics Review Committee of Shanghai Changhai Hospital (Approval Document No. Chec2016-107 and Chec2018-073), and was registered by the China Clinical Trial Registration Center (Registration No. ChiCTR - IOR - 17013875).
All participant were recruited in Department of Rehabilitation, Changhai hospital, and our trial was conducted from December 30, 2017 to December 31, 2019. For eligible participants who meet all reuired criteria, it was requested to sign the informed consent before randomization.
Inclusion criteria: ① patients meeting the diagnostic criteria of stroke with head CT/MRI confirmed by that cerebrovascular accident occurred in the internal carotid artery system, and vital signs stable for at least 48 hours; ② patients with unilateral spastic paralysis (that is, 0<MAS score≤3 and NIHSS score≥2) ; ③ patients with elevated muscle tone, enhanced tendon reflexes, with or without pathological reflexes and with no recent significant change in muscle tension within 2 weeks; ④ male or females 18-85 years old with the course of 2 weeks to 6 months; ⑤ patients not taking sedatives or muscle relaxants recently; ⑥ patients with informed consent signed.
Exclusion criteria: ① patients received other antispasmodic therapy that may affect the observed indicators and efficacy of this study; ② Pregnant or lactating women, or those with drug allergy history; ③ patients with cerebral apoplexy for 3 times or bilateral paralysis; ④ patients with increased muscle tension caused by noncerebrovascular disease (e.g., Brain trauma, brain tumors, brain parasitosis or heart disease); ⑤ patients with declined balance and coordination, or patients with cognitive-communication disorders; ⑥ patients with severe primary diseases(e.g., heart,liver, kidney or hematopoiesis diseases) or mental disease; ⑦ Patients with contraindications in rehabilitation, or filiform-needle, or FFN.
Data collection
Before treatment, observe and record the basic information of the included patients, such as name, gender, age, height, weight, hemiplegic side, stroke type, ID number, and subject number.All included participants were evaluated upper limb function to complete four scales including Modified Ashworth Scale(MAS),Fugl-Meyer Assessment of Upper Extremity Motor Function(FMA-UE),Activities of Daily Living(ADL),National Institutes of Health Stroke Scale(NIHSS)before treatment (T0) ,10-day (T1) and 20-day (T2) treatment and the 20th day after treatment (T3).
Randomization and blinding
Before the study, each patient will be randomly assigned one serial number generated by EXCEL 2013. Assignments were sealed in sequentially-coded and opaque envelopes, and be opened by the researchers following informed consent procedures and baseline testing. Then patients were randomly assigned to three groups according to the order of entry into the study. The assessors and statistician were blinded to the intervention. All therapists were not blinded to group assignments due to the nature of the intervention. Any premature unmasking of a participant would be noted and sent to the researchers.
Interventions
Patients randomly allocated to three different groups: (1) the Rehabilitation therapy group (R group) as the control group; (2) the Filiform-needle acupuncture group (A group); (3) the FFN acupuncture group (F group). The basic treatment of all enrolled patients was based on Guidelines for Adult Stroke Rehabilitation and Recovery[18] .
Rehabilitation treatment group (R group)
Rehabilitation training is formulated according to Guidelines for Adult Stroke Rehabilitation and Recovery of the American Heart Association/American Stroke Association[18]. Rehabilitation items of spasmodic paralysis include: physical modalities, postural training, neurodevelopmental therapy, electromyographic biofeedback and so on. The rehabilitation program was carried out 8 days in a row with 2-day break in 10 days for 20 days (that is, 16 times in total), and every time, the rehabilitation treatment lasted for approximately 30 minutes. All rehabilitation treatments were carried out by qualified professional therapists.
Filiform-needle acupuncture group (A group)
All participants in this group accepted filiform-needle acupuncture treatment on hemiplegic upper limb with the following acupoints: Jianyu(LI15), Hegu(LI4), Waiguan(SJ5), Quchi(LI11), Shousanli(LI10), Neiguan(PC6), Jiquan(HT1), Chize(LU5), Jianliao(TE-14). Skin was disinfected with 75% ethanol Before treatment, and disposable stainless steel needles (0.30×40mm, Suzhou Medical Appliance Factory, Suzhou, China) penetrate into each acupoint. After getting Deqi, a sense of acid, tingling, distension, and pain, needles should be maintained for 30 min and manipulated every 15 min. Moreover, all the filiform-needle therapy was performed by trained acupuncturists with professional qualification. The acupuncture course was the same as rehabilitation treatment.
Filiform-fire-needle acupuncture group (F group)
This group will accept FFN acupuncture treatment on the affected upper limb using the same acupoints used in A group. After skin sterilized, disposable stainless steel needles were heated until turning red, and swiftly inserted each acupoint to a depth of 15-25mm, and then pulled out quickly, which lasted less than 0.5 seconds. After each acupoint penetrated, pressure is applied to the insertion site with a alcohol cotton ball. For the acupuncturists performing FFN therapy, they should receive special training to achieve a sound understanding of FFN acupuncture intervention and to normalize the practices across different acupuncturists. The treatment was given every other day in 20 days (that is, 10 times in total).
Abnormal situation of acupuncture and its treatment measures
If abnormal conditions such as dizzy needles, bleeding and hematoma occur in the course of treatment, the treatment should be stopped immediately, the cause should be found, the degree should be evaluated, and targeted measures should be taken to eliminate the patient's discomfort, as detailed in schedule 1(Schedule 1).
Outcomes measures
The observation period covered the day before treatment (T0) to 10-day (T1) and 20-day (T2) treatment. Follow-ups were conducted at the 20th day after treatment (T3).
Primary outcome
-Modified Ashworth Scale(MAS)[19]
MAS can be used to assess the spasm and resistance of relaxed limbs to rapid passive stretching.In this study,the Modified Ashworth Scale is used to grade the upper limb spasticity. This is a 6-level rating scale with ratings from 0 to Ⅳ.A score of 0 indicates normal or slightly increased muscle tone,while IV indicates stiff limbs unable to move.
Refer to the "Guiding Principles for Clinical Research of New Chinese Medicines (Trial Version)" published by the Ministry of Health in 2002, and evaluate the efficacy according to the changes in the MAS rating, as follows (Table 1):
Secondary outcomes
-Fugl-Meyer Assessment of Upper Extremity Motor Function(FMA-UE)[20]
FMA-UR is the earliest and most widely used quantitative assessment scale for stroke motor function in the world, with high reliability and validity. It is divided into upper and lower limbs. The FMA-UE used in this study is the upper limb motor function part of FMA, including 10 major items and 33 small items, with a full score of 66 points. Evaluate the recovery of upper limb function from the aspects of fine movement, tendon reflex, coordination ability.The lower the total score, the worse the upper limb function.
-Activity of Daily Living Scale (ADL)[21]
ADL consists of the Physical Self-maintenance Scale and the instrument activity of Daily Living Scale, which are used to assess participants’ ability to perform tasks of daily living. ADL includes 14 main items, with a maximum score of 64. The evaluation results can be analyzed according to the total score, scale score and individual items. The total score is less than 16 points as completely normal, and the total score is greater than 16 points as functional decline. This study used the Barthel Index (BI) scale for evaluation, which is very important for evaluating the disability level of patients, assisting in the formulation of rehabilitation plans, and quantifying functional changes.
-National Institutes of Health Stroke Scale(NIHSS) [22]
NIHSS can comprehensively assess stroke symptoms, and is mainly used for disease judgment, plan formulation, efficacy evaluation and outcome prediction, including 13 meaningful items selected from the Toronto Stroke Scale, the Oxbury Initial Severity Scale and the Cincinnati Stroke Scale. The scale evaluates patients with 13 items in 11 aspects including level of consciousness, gaze, visual field, facial paralysis, limb movement, ataxia, sensation, speech, and neglect. Divided into three levels: light, medium and heavy (light = 0-4 points; medium: = 5-10 points; heavy 11 points)
Safety evaluation
A self-made abnormal observation table was used (Schedule 1). After each treatment, if adverse events or adverse reactions occur during the trial, the category, degree, duration, treatment measures, treatment results, etc., should be recorded in detail, and on the basis of comprehensive consideration of complications and combined use of drugs, evaluate its correlation with treatment measures. In addition, when adverse events and adverse reactions are found, the person in charge of the study can determine whether to stop the trial according to the condition, and follow up the cases that stop treatment due to adverse events and adverse reactions.
Statistical analysis
A sample size calculation was determined based on our previous study, in which the effective rates were 83.3%, 60.0% and 50.0%. To detect a significant difference between any two groups with a 80%-power of 80% and a two-side 5% significance, these relevant parameters (83.3%, 60.0%, 50.0%; α = 0.05, 1 -β = 0.9) were input into NCSS-PASS 11, and the calculated number of patients was about 36 per treatment group. Considering an estimated dropout rate of 20%, the total sample size needs 129 initial patients with 60 per group.
SPSS 21.0 software was used to analyze the collected data. Data are expressed as mean ± standard deviation ± s) or median (interval). Analysis of variance, chi-square test,and rank sum test were used to test the balance of the general information of the three groups of patients (including age, gender, BMI, etc。) . Generalized estimation equations or repeated measurement data analysis of variance were used to compare the scores of each scale between time-points.Data were tested for normality and variance homogeneity before further analysis. P<0.05 was considered to indicate a statistically significant difference.The statistical analysis of data is done by professionals independently who are not participate in the recruitment and treatment of patients, and the researchers and operators work.