NCT06893185

Brief Summary

Cervical spondylosis is one of the common causes of chronic neck pain. It can significantly affect the quality of life, lead to disabilities, and increase the economic burden on patients. Treatment mainly includes pain relievers, non-steroidal anti-inflammatory drugs (NSAIDs), muscle relaxants or physical therapy. The condition tends to recur frequently; therefore, long-term use of medication can lead to unwanted effects on the digestive system, kidneys, and cardiovascular system. Dry cupping therapy is a non-pharmacological method that has been shown to be effective in pain management. Cupping therapy has the advantage of being applicable to patients who are afraid of needles and has a wide area of effect. Given the limitations in evaluating treatment effectiveness and safety, along with the lack of published research discussing the analgesic effects of dry cupping for neck pain caused by cervical spondylosis, the investigators conducted the study on pain reduction and safety of cupping therapy in patients with neck pain caused by cervical spondylosis.

Trial Health

35
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
82

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Jun 2025

Shorter than P25 for not_applicable

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

March 18, 2025

Completed
7 days until next milestone

First Posted

Study publicly available on registry

March 25, 2025

Completed
2 months until next milestone

Study Start

First participant enrolled

June 1, 2025

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 31, 2025

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

August 31, 2025

Completed
Last Updated

May 29, 2025

Status Verified

April 1, 2025

Enrollment Period

2 months

First QC Date

March 18, 2025

Last Update Submit

May 23, 2025

Conditions

Keywords

Neck PainCupping therapyCervical spondylosis

Outcome Measures

Primary Outcomes (1)

  • The change of the Visual Analog Scale (VAS)

    Symptom scores will be assessed based on a visual analogue scale (VAS). It usually consists of a 10 cm line anchored at each end by descriptors. Patients will be classified into 1 of 4 groups (no pain (0 cm), mild pain (1-3 cm), moderate pain (4-7 cm), severe pain (8-10 cm)).

    Assessments were conducted before intervention and after each intervention week throughout the two weeks (Week 0, Week 1, Week 2)

Secondary Outcomes (2)

  • Proportion of intervention-related adverse events

    Assessments were conducted after each intervention week throughout the two weeks.

  • Active range of motion of the cervical spine

    Assessments were conducted before intervention and after each intervention week throughout the two weeks (Week 0, Week 1, Week 2)

Study Arms (2)

Dry cupping Group

EXPERIMENTAL

Dry cupping therapy every 3 days for a total of two weeks (5 sessions)

Other: Dry cupping therapy

Electroacupuncture Group

ACTIVE COMPARATOR

Electroacupuncture five times a week for a total of two weeks (10 sessions)

Other: Electroacupuncture

Interventions

Dry cupping therapy will perform on the skin areas containing the EX-B2, A-shi, and GB21 acupuncture points every 3 days for 2 weeks.

Dry cupping Group

Electroacupuncture therapy will be performed five times a week for 2 weeks. The acupoints are the Huatuojiaji (EX-B2), A-shi, and Jianjing (GB21).

Electroacupuncture Group

Eligibility Criteria

Age20 Years - 60 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • Individuals between the ages of 20 and 60 years, outpatient treatment.
  • Individuals diagnosed with cervical spondylosis.
  • Individuals report pain intensity between 3 and 8 according to on the Visual Analogue Scale (VAS) on the screening visit day.
  • Experiencing neck pain for no longer than four weeks.
  • Individuals who volunteered to participate in the study and signed a consent form.

You may not qualify if:

  • Patients diagnosed with acute or chronic neck pain due to specific causes or with root compression syndrome, spinal cord compression syndrome, or vertebral artery syndrome.
  • Patients loss of normal cervical curvature or deformity.
  • Individuals with a history of neck trauma, cervical vertebra fracture, or cervical spine surgery, congenital spinal abnormalities, systemic bone and joint diseases.
  • Patients have undergone cupping therapy, plastering, or drug inhalation within one week prior to participating in the study.
  • Patients used of medications that could affect research outcomes within one week: Pain relievers, muscle relaxants, traditional medicines for treating neck pain.
  • Patients suffer from a mental illness or lacks consciousness.
  • Patients have a pacemaker, or any metal devices such as screws or plates.
  • Patients currently using anticoagulant medications or has a bleeding disorder.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Related Publications (8)

  • Kim S, Kim E, Jung G, Lee S, Kim JG. The hemodynamic changes during cupping therapy monitored by using an optical sensor embedded cup. J Biophotonics. 2019 May;12(5):e201800286. doi: 10.1002/jbio.201800286. Epub 2019 Jan 28.

    PMID: 30604505BACKGROUND
  • Gao C, Wang M, He L, He Y, Li T. Alternations of hemodynamic parameters during Chinese cupping therapy assessed by an embedded near-infrared spectroscopy monitor. Biomed Opt Express. 2018 Dec 12;10(1):196-203. doi: 10.1364/BOE.10.000196. eCollection 2019 Jan 1.

    PMID: 30775093BACKGROUND
  • Kolenkiewicz M, Wlodarczyk A, Wojtkiewicz J. Diagnosis and Incidence of Spondylosis and Cervical Disc Disorders in the University Clinical Hospital in Olsztyn, in Years 2011-2015. Biomed Res Int. 2018 Mar 25;2018:5643839. doi: 10.1155/2018/5643839. eCollection 2018.

    PMID: 29770333BACKGROUND
  • Peng AT, Behar S, Yue SJ. Long-term therapeutic effects of electro-acupuncture for chronic neck and shoulder pain--a double blind study. Acupunct Electrother Res. 1987;12(1):37-44. doi: 10.3727/036012987816358922.

    PMID: 2883835BACKGROUND
  • Zhang SP, Chiu TT, Chiu SN. Long-term efficacy of electroacupuncture for chronic neck pain: a randomised controlled trial. Hong Kong Med J. 2013 Dec;19 Suppl 9:36-9.

    PMID: 24473589BACKGROUND
  • Chi LM, Lin LM, Chen CL, Wang SF, Lai HL, Peng TC. The Effectiveness of Cupping Therapy on Relieving Chronic Neck and Shoulder Pain: A Randomized Controlled Trial. Evid Based Complement Alternat Med. 2016;2016:7358918. doi: 10.1155/2016/7358918. Epub 2016 Mar 17.

    PMID: 27073404BACKGROUND
  • Kim S, Lee SH, Kim MR, Kim EJ, Hwang DS, Lee J, Shin JS, Ha IH, Lee YJ. Is cupping therapy effective in patients with neck pain? A systematic review and meta-analysis. BMJ Open. 2018 Nov 5;8(11):e021070. doi: 10.1136/bmjopen-2017-021070.

    PMID: 30397006BACKGROUND
  • Haldeman S, Carroll L, Cassidy JD. Findings from the bone and joint decade 2000 to 2010 task force on neck pain and its associated disorders. J Occup Environ Med. 2010 Apr;52(4):424-7. doi: 10.1097/JOM.0b013e3181d44f3b.

    PMID: 20357682BACKGROUND

MeSH Terms

Conditions

Neck PainSpondylosis

Interventions

Electroacupuncture

Condition Hierarchy (Ancestors)

PainNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and SymptomsSpinal DiseasesBone DiseasesMusculoskeletal Diseases

Intervention Hierarchy (Ancestors)

Combined Modality TherapyTherapeuticsAcupuncture TherapyComplementary TherapiesElectric Stimulation TherapyPhysical Therapy ModalitiesRehabilitationTranscutaneous Electric Nerve StimulationAnalgesiaAnesthesia and AnalgesiaAnesthesia

Central Study Contacts

Phuong Ngoc Ha Dang

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

March 18, 2025

First Posted

March 25, 2025

Study Start

June 1, 2025

Primary Completion

July 31, 2025

Study Completion

August 31, 2025

Last Updated

May 29, 2025

Record last verified: 2025-04