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Clinical Evaluation for Digital Acupuncture Manipulation Therapeutic Instrument

Primary Purpose

Cervical Spondylosis

Status
Unknown status
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Digital Acupuncture Manipulation Therapeutic Instrument
Manual Acupuncture
Sham Acupuncture
Sponsored by
Shanghai University of Traditional Chinese Medicine
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Cervical Spondylosis focused on measuring digital acupuncture manipulation therapeutic instrument, cervical spondylosis

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

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

Sites / Locations

  • LongHua Hospital Shanghai University of Traditional Chinese MedicineRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Active Comparator

Sham Comparator

Arm Label

Digital Acupuncture Instrument Group

Manual Acupuncture Group

Sham Acupuncture Group

Arm Description

The needles will be stimulated manually to achieve de qi (a compositional sensation including soreness, numbness, distention and heaviness) and then paired electrodes from the digital acupuncture instrument will be attached to the needle handles and another two adjunct acupoints by the research assistant. The electric current will be increased until the needles begin to vibrate slightly.

Patients in the MA group will undergo similar procedures as the EA group except that no current will be output from the instrument.

Patients in the SA group will receive non-invasive acupuncture to avoid de qi.

Outcomes

Primary Outcome Measures

Visual Analogue scale(VAS)
A graphic scale that helps a patient to quantify pain, depression, and other subjective and otherwise unmeasurable states or conditions.
Visual Analogue scale(VAS)
A graphic scale that helps a patient to quantify pain, depression, and other subjective and otherwise unmeasurable states or conditions.

Secondary Outcome Measures

Neck Disability Index(NDI)
A scale that helps a patient to quantify neck disability.
short form 36-item questionnaire, SF-36
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.

Full Information

First Posted
August 11, 2020
Last Updated
September 1, 2021
Sponsor
Shanghai University of Traditional Chinese Medicine
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1. Study Identification

Unique Protocol Identification Number
NCT04525651
Brief Title
Clinical Evaluation for Digital Acupuncture Manipulation Therapeutic Instrument
Official Title
Clinical Evaluation for Digital Acupuncture Manipulation Therapeutic Instrument
Study Type
Interventional

2. Study Status

Record Verification Date
September 2021
Overall Recruitment Status
Unknown status
Study Start Date
January 1, 2021 (Actual)
Primary Completion Date
September 30, 2022 (Anticipated)
Study Completion Date
December 31, 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Shanghai University of Traditional Chinese Medicine

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cervical Spondylosis
Keywords
digital acupuncture manipulation therapeutic instrument, cervical spondylosis

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
150 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Digital Acupuncture Instrument Group
Arm Type
Experimental
Arm Description
The needles will be stimulated manually to achieve de qi (a compositional sensation including soreness, numbness, distention and heaviness) and then paired electrodes from the digital acupuncture instrument will be attached to the needle handles and another two adjunct acupoints by the research assistant. The electric current will be increased until the needles begin to vibrate slightly.
Arm Title
Manual Acupuncture Group
Arm Type
Active Comparator
Arm Description
Patients in the MA group will undergo similar procedures as the EA group except that no current will be output from the instrument.
Arm Title
Sham Acupuncture Group
Arm Type
Sham Comparator
Arm Description
Patients in the SA group will receive non-invasive acupuncture to avoid de qi.
Intervention Type
Device
Intervention Name(s)
Digital Acupuncture Manipulation Therapeutic Instrument
Intervention Description
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.
Intervention Type
Other
Intervention Name(s)
Manual Acupuncture
Intervention Description
Manual acupuncture to acheive de qi.
Intervention Type
Other
Intervention Name(s)
Sham Acupuncture
Intervention Description
Sham acupuncture to avoid de qi.
Primary Outcome Measure Information:
Title
Visual Analogue scale(VAS)
Description
A graphic scale that helps a patient to quantify pain, depression, and other subjective and otherwise unmeasurable states or conditions.
Time Frame
Change from baseline VAS at 4weeks
Title
Visual Analogue scale(VAS)
Description
A graphic scale that helps a patient to quantify pain, depression, and other subjective and otherwise unmeasurable states or conditions.
Time Frame
Change from baseline VAS at 8weeks
Secondary Outcome Measure Information:
Title
Neck Disability Index(NDI)
Description
A scale that helps a patient to quantify neck disability.
Time Frame
Baseline(Week 0), After treatment(Week 4), Follow-up(Week 8)
Title
short form 36-item questionnaire, SF-36
Description
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.
Time Frame
Baseline(Week 0), After treatment(Week 4), Follow-up(Week 8)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Neck pain with the diagnosis of cervical spondylotic radiculopathy; Aged between 18-70 years; Have not participated in any drug clinical trials within the last month; Voluntarily joining this study with informed consents Exclusion Criteria: A history of cervical spine trauma or have received cervical spine surgery; Accompanied by obvious dizziness and spinal cord compression symptoms or imaging findings of spinal cord compression; Cervical spondylosis in urgent need of surgery; Pregnant women and lactating women; A serious heart condition, hepatic disease, renal system disease, hematopoietic system disease, or whole-body malnutrition Anticoagulant treatments such as warfarin or heparin use of pacemakers or receiving acupuncture in the past 2 weeks
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jian Pei, Doctor
Phone
00862164385700
Ext
3534
Email
longhuaacup@aliyun.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jian Pei, Doctor
Organizational Affiliation
Shanghai University of Traditional Chinese Medicine
Official's Role
Study Chair
Facility Information:
Facility Name
LongHua Hospital Shanghai University of Traditional Chinese Medicine
City
Shanghai
State/Province
Shanghai
ZIP/Postal Code
200032
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jian Pei, Doctor
Phone
00862164385700
Ext
3534
Email
jianpei99@hotmail.com

12. IPD Sharing Statement

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Clinical Evaluation for Digital Acupuncture Manipulation Therapeutic Instrument

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