Intelligent Moxibustion Robot in the Treatment of Low Back Pain

Low Back Pain Clinical Trial

Official title:

Clinical Study of Intelligent Moxibustion Robot in the Treatment of Low Back Pain: a Randomized Controlled Clinical Trial

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05704127
• Other study ID #: ShanxiAcupuncture
• Status: Recruiting
• Phase: N/A
• Start date: December 15, 2022
• Est. completion date: December 31, 2023

Study information

• Verified date: January 2023
• Source: Shanxi Acupuncture and Moxibustion Hospital
• Contact: Bosong Hou, Postgraduate
• Phone: 0086 18337320205
• Email: 904225587[@]qq.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The intelligent moxibustion robot is applied to the clinical treatment of low back pain to verify its effectiveness and safety

Description:

Shanxi Acupuncture and Moxibustion Hospital and North University of China jointly developed an "intelligent thunder-fire moxibustion" robot with six degrees of freedom mechanical arm as the core and will be applied in clinical practice to verify its clinical efficacy. In clinical practice, patients with low back pain were recruited jointly by several hospitals and divided into two groups. Intelligent thunder-fire moxibustion robot and artificial thunder-fire moxibustion were respectively used for treatment. The clinical efficacy and safety of intelligent thunder-fire moxibustion robot were evaluated through comparative analysis of outcome indexes such as VAS pain scale and serum inflammatory factors.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 160
• Est. completion date: December 31, 2023
• Est. primary completion date: October 31, 2023
• Accepts healthy volunteers: No
• Gender: All
• Age group: 25 Years to 70 Years

Eligibility

Inclusion Criteria:

• 1.It is consistent with the diagnostic criteria of low back pain and the syndrome differentiation criteria of cold and wet lumbar muscle strain.

• 2.There is no gender limitation, and the age should be between 25 and 70 years old

• 3.No treatment of traditional Chinese and western medicine related to lumbago was received in the past 2 weeks

• 4.The course of disease was controlled within 8 years

• 5.Informed consent, willing to cooperate with the whole treatment

• 6.Agree to record the scale score and volunteer to participate in this experiment

• 7.At least one contact information should be reserved for patients to receive follow-up visits

• 8.In order to reduce the rate of shedding, priority is included in hospitalized patients

Exclusion Criteria:

• 1.Patients do not meet the inclusion criteria Patients who do not meet the diagnostic inclusion criteria of this subject

• 2.The patient is in the pregnancy or lactation period

• 3.Patients are allergic to moxibustion smoke, and it is difficult to accept moxibustion treatment

• 4.The patient suffers from diseases of the blood and immune system

• 5.Patients with cardiac, liver and renal insufficiency

• 6.The patient suffers from mental illness and cannot cooperate with moxibustion

• 7.The patient suffered from lumbar spine tuberculosis, bone cancer and other diseases, which affected the experimental results

Related Conditions & MeSH terms

• Back Pain
• Low Back Pain
• Moxibustion

Intervention

Other:
• Intelligent Moxibustion Robot
The intelligent moxibustion robot holds the thunder fire moxibustion stick and conducts suspension moxibustion treatment on the points BL23, BL25, DU3 and pain points for 10 minutes in each group, a total of 40 minutes. BL23 and BL25 have one acupuncture point on each side of the spine, and the straight line reciprocating moxibustion technique is adopted. DU3, a single point, adopts the whirling moxibustion technique. Pain points,according to the number of pain points, choose straight reciprocating moxibustion or rotary moxibustion.
• Artificial moxibustion
The people hold the thunder fire moxibustion stick and conducts suspension moxibustion treatment on the points BL23, BL25, DU3 and pain points for 10 minutes in each group, a total of 40 minutes. BL23 and BL25 have one acupuncture point on each side of the spine, and the straight line reciprocating moxibustion technique is adopted. DU3, a single point, adopts the whirling moxibustion technique. Pain points,according to the number of pain points, choose straight reciprocating moxibustion or rotary moxibustion.

Locations

Country	Name	City	State
China	Lingqiu Hospital of Traditional Chinese Medicine	Datong	Shanxi
China	Shanxi Acupuncture and moxibustion Hospital	Taiyuan	Shanxi
China	Xinghualing Hospital of Traditional Chinese Medicine	Taiyuan	Shanxi
China	Yongji Hospital of Traditional Chinese Medicine	Yuncheng	Shanxi

Sponsors (5)

Lead Sponsor	Collaborator
Shanxi Acupuncture and Moxibustion Hospital	Lingqiu Hospital of Traditional Chinese Medicine, Datong City,Shanxi Province,China, North University of China, Xinghualing Hospital of Traditional Chinese Medicine, Taiyuan City, Shanxi Province,China, Yongji Hospital of Traditional Chinese Medicine, Yuncheng City,Shanxi Province,China

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Visual analogue scale(VAS score)	visual analogue scale (VAS) was used to assess pain. It is widely used in clinical practice in China. The basic method is to use a walking scale about 10cm long, with 10 scales on one side and "0" and "10" respectively at both ends. 0 points means no pain and 10 points means the most unbearable pain.(On a scale of 0-10, the lower the score, the better the health)	Before enrollment
Primary	Visual analogue scale(VAS score)	visual analogue scale (VAS) was used to assess pain. It is widely used in clinical practice in China. The basic method is to use a walking scale about 10cm long, with 10 scales on one side and "0" and "10" respectively at both ends. 0 points means no pain and 10 points means the most unbearable pain.(On a scale of 0-10, the lower the score, the better the health)	After 5 treatments, an average of 1 week
Primary	Visual analogue scale(VAS score)	visual analogue scale (VAS) was used to assess pain. It is widely used in clinical practice in China. The basic method is to use a walking scale about 10cm long, with 10 scales on one side and "0" and "10" respectively at both ends. 0 points means no pain and 10 points means the most unbearable pain.(On a scale of 0-10, the lower the score, the better the health)	Through all treatments -- after 10 treatments, an average of 2 week
Primary	Visual analogue scale(VAS score)	visual analogue scale (VAS) was used to assess pain. It is widely used in clinical practice in China. The basic method is to use a walking scale about 10cm long, with 10 scales on one side and "0" and "10" respectively at both ends. 0 points means no pain and 10 points means the most unbearable pain.(On a scale of 0-10, the lower the score, the better the health)	2 weeks after treatment
Primary	Japanese Orthopaedic Association Score--Low Back Pain(JOA Low Back Pain Score)	The questionnaire was designed to understand the impact of patients' low back pain on daily activities. According to their own conditions, the patients choose a most consistent or close answer under each item, and ultimately by the sum of scores to judge the severity of low back pain.(On a scale of 0-29, the higher the score, the better the health)	Before enrollment
Primary	Japanese Orthopaedic Association Score--Low Back Pain(JOA Low Back Pain Score)	The questionnaire was designed to understand the impact of patients' low back pain on daily activities. According to their own conditions, the patients choose a most consistent or close answer under each item, and ultimately by the sum of scores to judge the severity of low back pain.(On a scale of 0-29, the higher the score, the better the health)	After 5 treatments, an average of 1 week
Primary	Japanese Orthopaedic Association Score--Low Back Pain(JOA Low Back Pain Score)	The questionnaire was designed to understand the impact of patients' low back pain on daily activities. According to their own conditions, the patients choose a most consistent or close answer under each item, and ultimately by the sum of scores to judge the severity of low back pain.(On a scale of 0-29, the higher the score, the better the health)	Through all treatments -- after 10 treatments, an average of 2 week
Primary	Japanese Orthopaedic Association Score--Low Back Pain(JOA Low Back Pain Score)	The questionnaire was designed to understand the impact of patients' low back pain on daily activities. According to their own conditions, the patients choose a most consistent or close answer under each item, and ultimately by the sum of scores to judge the severity of low back pain.(On a scale of 0-29, the higher the score, the better the health)	2 weeks after treatment
Primary	36-items short form health survey(SF-36)	As a concise health questionnaire, the SF-36 comprehensively summarizes the quality of life of the respondents from eight aspects: physiological function, physiological function, physical pain, general health status, energy, social function, emotional function and mental health.(On a scale of 0-149, the higher the score, the better the health)	Before enrollment
Primary	36-items short form health survey(SF-36)	As a concise health questionnaire, the SF-36 comprehensively summarizes the quality of life of the respondents from eight aspects: physiological function, physiological function, physical pain, general health status, energy, social function, emotional function and mental health.(On a scale of 0-149, the higher the score, the better the health)	After 5 treatments, an average of 1 week
Primary	36-items short form health survey(SF-36)	As a concise health questionnaire, the SF-36 comprehensively summarizes the quality of life of the respondents from eight aspects: physiological function, physiological function, physical pain, general health status, energy, social function, emotional function and mental health.(On a scale of 0-149, the higher the score, the better the health)	Through all treatments -- after 10 treatments, an average of 2 week
Primary	36-items short form health survey(SF-36)	As a concise health questionnaire, the SF-36 comprehensively summarizes the quality of life of the respondents from eight aspects: physiological function, physiological function, physical pain, general health status, energy, social function, emotional function and mental health.(On a scale of 0-149, the higher the score, the better the health)	2 weeks after treatment
Primary	Roland Morris Disability Questionnaire(RMDQ)	The questionnaire was designed to understand the impact of patients' low back pain on daily activities. Patients choose the most consistent or close answer under each item, depending on their situation. The questionnaire consisted of 24 questions closely related to low back pain. The actual score ranges from 0 to 24, with higher scores indicating more serious dysfunction.(On a scale of 0-24, the lower the score, the better the health)	Before enrollment
Primary	Roland Morris Disability Questionnaire(RMDQ)	The questionnaire was designed to understand the impact of patients' low back pain on daily activities. Patients choose the most consistent or close answer under each item, depending on their situation. The questionnaire consisted of 24 questions closely related to low back pain. The actual score ranges from 0 to 24, with higher scores indicating more serious dysfunction.(On a scale of 0-24, the lower the score, the better the health)	After 5 treatments, an average of 1 week
Primary	Roland Morris Disability Questionnaire(RMDQ)	The questionnaire was designed to understand the impact of patients' low back pain on daily activities. Patients choose the most consistent or close answer under each item, depending on their situation. The questionnaire consisted of 24 questions closely related to low back pain. The actual score ranges from 0 to 24, with higher scores indicating more serious dysfunction.(On a scale of 0-24, the lower the score, the better the health)	Through all treatments -- after 10 treatments, an average of 2 week
Primary	Roland Morris Disability Questionnaire(RMDQ)	The questionnaire was designed to understand the impact of patients' low back pain on daily activities. Patients choose the most consistent or close answer under each item, depending on their situation. The questionnaire consisted of 24 questions closely related to low back pain. The actual score ranges from 0 to 24, with higher scores indicating more serious dysfunction.(On a scale of 0-24, the lower the score, the better the health)	2 weeks after treatment
Primary	Lumbar joint range of motion	A professional protractor was used to measure the range of motion in six azimuths of waist, anterior flexion, posterior extension, left and right lateral flexion and left and right rotation in the upright position, and the degree of movement was recorded.	Before enrollment
Primary	Lumbar joint range of motion	A professional protractor was used to measure the range of motion in six azimuths of waist, anterior flexion, posterior extension, left and right lateral flexion and left and right rotation in the upright position, and the degree of movement was recorded.	Through all treatments -- after 10 treatments, an average of 2 week
Primary	Schober test	Subjects stood upright and were marked 5cm below and 10cm above the lumbosacral junction. Subjects were asked to bend forward as far as possible and the distance (cm) between the lumbosacral junction and the marker was measured. The increased distance was used to represent lumbar range of motion.	Before enrollment
Primary	Schober test	Subjects stood upright and were marked 5cm below and 10cm above the lumbosacral junction. Subjects were asked to bend forward as far as possible and the distance (cm) between the lumbosacral junction and the marker was measured. The increased distance was used to represent lumbar range of motion.	Through all treatments -- after 10 treatments, an average of 2 week
Primary	Serum inflammatory response factor	4 mL of venous blood was drawn from patients before and after treatment, and serum was separated and detected by ELISA. Serum tumor necrosis factor (TNF-a), interleukin IL-1ß, interleukin IL-6, and serum thromboxane B2 (TXB2) were measured.	Before enrollment
Primary	Serum inflammatory response factor	4 mL of venous blood was drawn from patients before and after treatment, and serum was separated and detected by ELISA. Serum tumor necrosis factor (TNF-a), interleukin IL-1ß, interleukin IL-6, and serum thromboxane B2 (TXB2) were measured.	Through all treatments -- after 10 treatments, an average of 2 week