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Clinical Evaluation for Digital Acupuncture Manipulation Therapeutic Instrument

Clinical Evaluation for Digital Acupuncture Manipulation Therapeutic Instrument

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04525651
Enrollment
150
Registered
2020-08-25
Start date
2021-01-01
Completion date
2022-12-31
Last updated
2021-09-10

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

Conditions

Cervical Spondylosis

Keywords

digital acupuncture manipulation therapeutic instrument, cervical spondylosis

Brief summary

The investigators design a randomized, control study to evaluate the therapeutic effect of digital acupuncture instrument in cervical spondylotic radiculopathy patients using the following outcomes: the Visual analogue scale(VAS), neck disability index scale (NDI) and short form 36-item questionnaire (SF-36).

Detailed description

Based on the digital acupuncture manipulation therapeutic instrument developed in the previous stage, the acupuncture manipulation acquisition system is used to compare and analyze the analog waves output by the experts' acupuncture manipulation and the manipulative therapeutic apparatus in the system data analysis module, in order to verify the consistency of bioelectric signals of different reinforcing and reducing manipulation of acupuncture and experts' manipulation. The biocompatibility of shock wave was detected by Massachusetts General Hospital Needle sensation scale ((Massachusetts General Hospital Acupuncture Sensation Scale, MASS)). The visual analogue pain score ((Visual analogue scale, VAS)), neck disability index scale ((Neck Disability Index,NDI) and short form 36-item questionnaire (SF-36) were used to evaluate the clinical efficacy and safety of the instrument in the treatment of cervical pain in cervical Spondylotic radiculopathy, and the appropriate syndrome type of the scheme was studied.

Interventions

DEVICEDigital Acupuncture Manipulation Therapeutic Instrument

The device is based on the characteristics of traditional acupuncture manipulation of Shanghai School of Traditional Chinese Medicine, and absorbs the information of the techniques of famous experts, modulates the stimulation waveform of the electroacupuncture device by modulating the signal, and realizes the digitization of acupuncture technique information.

Manual acupuncture to acheive de qi.

OTHERSham Acupuncture

Sham acupuncture to avoid de qi.

Sponsors

Shanghai University of Traditional Chinese Medicine
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
Yes

Inclusion criteria

1. Neck pain with the diagnosis of cervical spondylotic radiculopathy; 2. Aged between 18-70 years; 3. Have not participated in any drug clinical trials within the last month; 4. Voluntarily joining this study with informed consents

Exclusion criteria

1. A history of cervical spine trauma or have received cervical spine surgery; 2. Accompanied by obvious dizziness and spinal cord compression symptoms or imaging findings of spinal cord compression; 3. Cervical spondylosis in urgent need of surgery; 4. Pregnant women and lactating women; 5. A serious heart condition, hepatic disease, renal system disease, hematopoietic system disease, or whole-body malnutrition 6. Anticoagulant treatments such as warfarin or heparin use of pacemakers or receiving acupuncture in the past 2 weeks

Design outcomes

Primary

MeasureTime frameDescription
Visual Analogue scale(VAS)Change from baseline VAS at 4weeksA graphic scale that helps a patient to quantify pain, depression, and other subjective and otherwise unmeasurable states or conditions.

Secondary

MeasureTime frameDescription
Neck Disability Index(NDI)Baseline(Week 0), After treatment(Week 4), Follow-up(Week 8)A scale that helps a patient to quantify neck disability.
short form 36-item questionnaire, SF-36Baseline(Week 0), After treatment(Week 4), Follow-up(Week 8)a set of 36 questions abstracted from the much longer set of several hundred used in household interview surveys of the U.S. National Health Survey. The SF36 questions are a convenient abbreviation, used for screening purposes to assess the physical function, social function, role limitation, mental health, energy, vitality, pain, and subjective perception of health status. They have been tested and found to be valid and reliable.

Countries

China

Contacts

Primary ContactJian Pei, Doctor
longhuaacup@aliyun.com00862164385700

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026