ClinicalTrials.gg
Status unknownNCT00826215Updated Jan 22, 2009

Electroacupuncture for Chronic Neck Pain

A Phase 2 interventional study of electroacupuncture and Sham laser acupuncture in Neck Pain, sponsored by Hong Kong Baptist University. Status unknown. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2009-01-22.

Sponsored by Hong Kong Baptist University · Phase 2, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Jan 2009), so the status shown — last known as Active, not recruiting — may be out of date.
Phase
Phase 2
Study type
Interventional
Enrollment
200
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

Objective: The primary objective of this study is to evaluate the long-term efficacy of electroacupuncture for chronic neck pain. The secondary objective is to document any possible side effects of acupuncture.

Design and Subjects: Prospective, randomised controlled trial comparing the outcomes of treatment and placebo interventions. Subjects are 200 adult patients with chronic mechanical neck pain.

Setting: Outpatient clinics.

Interventions: Patients will be randomly allocated to one of the two groups receiving either: electroacupuncture (real treatment) or placebo (sham laser acupuncture). Each treatment will last for 45 minutes. Each patient will receive a total of nine treatments (three times per week for three weeks).

Main outcome measures:

Primary outcome measures: Neck pain disability index (Northwick Park Neck Pain Questionnaire).

Secondary outcome measures: Maximum pain related to motion on visual analogue scale. Quality of life (SF-36). Use of medication. Sick leave because of neck pain. Treatment-related adverse effects, such as pain, skin irritation, bleeding and dizziness, will also be assessed.

Assessments will be made before treatment, one month, three months and six months after the treatment course. The credibility of placebo treatment will also be assessed.

Expected results: We expect that patients in the treatment group will have significant improvements on primary and secondary outcome measures, when compared with patients in the inert placebo group.

Conclusion: This study will provide credible evidence regarding whether electroacupuncture is effective in reducing chronic neck pain. Patients, healthcare professionals, and government policy makers can make use of this information to improve clinical outcomes and reduce costs

02

Conditions studied

  • Neck Pain

Keywords

  • mechanical
  • neck pain
  • chronic
  • acupuncture
  • chronic mechanical neck pain
03

In context

Neck Pain

1,259 studies on the registry are indexed under Neck Pain; 256 are open to participants now.

This study's planned enrollment of 200 is above the median of 52 across 1,026 interventional studies indexed under Neck Pain.

Browse Neck Pain studies →

Lead sponsor

Hong Kong Baptist University is the lead sponsor of 84 studies on the registry; 23 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Adult male or female subjects age above 18 with mechanical neck pain for over three months.

Exclusion criteria

Exclusion Criteria:

  • Patients who have received acupuncture treatment for any purpose in the last 6 months.
  • Patients who will be unlikely to attend all treatment sessions.
  • Patients with systemic diseases, such as diabetes or cardiovascular disorder.
  • Patients with a history of traumatic injury of the neck or upper back from T1-T6, precious fracture or surgery to the neck, neurological deficits (e.g., muscle weakness or changes in spinal reflex jerks), a history of malignancy, congenital abnormality of the spine, or systemic bone and joint disorders (e.g., RA).
  • Patients who are seeking compensation for neck-related condition.
  • Patients who have needle phobia.
  • Pregnant and breast feeding women.
05

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Triple (Participant, Investigator, Outcomes assessor)
Enrollment
200 participants (estimated)

Study arms

  • Experimental
    1

    Electroacupuncture treatment

    Device: electroacupuncture

  • Sham comparator
    2

    Sham laser acupuncture

    Device: Sham laser acupuncture

Interventions

  • Deviceelectroacupuncture

    Nine sections of 45 minutes electroacupuncture treatment in three weeks

  • DeviceSham laser acupuncture

    Sham laser acupuncture

06

What researchers measure

Primary outcomes

  1. Change in neck pain specific disability index as measured by the Northwick Park Neck Pain Questionnaire (NPQ).

    Time frame: 6 months

Secondary outcomes

  1. i) Change in maximum pain related to motion, regardless the direction of movement. ii) Quality of life as assessed by SF-36 health survey. iii) Use of medication because of neck pain iv) Sick leave because of neck pain.

    Time frame: 6 months

  2. Adverse effects.

    Time frame: 6 months

07

Study locations

No study locations are listed for this record.

08

Timeline

Tracking since Sep 25, 2026
Not marked actual or estimatedDates not marked actual or estimated

The record gives a start of Mar 2007, a primary completion of Feb 2009 and a completion of Feb 2009. It does not say whether these dates are actual or estimated.

How these figures are worked out, and which studies are left out of them.

Registered
Jan 21, 2009
First posted
Jan 22, 2009
Start
Mar 2007
Primary completionEst.
Feb 2009
CompletionEst.
Feb 2009
Last update
Jan 22, 2009
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Jan 22, 2009, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT00826215
Lead sponsor
Hong Kong Baptist University
First posted
Jan 22, 2009
Start date
Mar 2007
Primary completion
Feb 2009 (estimated)
Completion
Feb 2009 (estimated)
Last update
Jan 22, 2009

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Jan 2009. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion