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CompletedNCT01233180Updated Feb 23, 2011

Effects of Gua Sha and Thermotherapy on Chronic Neck Pain

An interventional study of Gua Sha and Thermotherapy in Neck Pain, sponsored by Universität Duisburg-Essen. Completed at 1 site in Germany. Open to participants aged 18 Years to 75 Years. Per ClinicalTrials.gov, last updated 2011-02-23.

Sponsored by Universität Duisburg-Essen · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
50
Allocation
Randomized
Ages
18 Years to 75 Years
Sex
All
01

Study summary

Gua Sha massage is a traditional chinese medical treatment. It is mostly used in the treatment of the common cold and pain syndromes. Gua Sha involves pressuring the skin by a round-edged instrument until small petechiae appear. This so called "sha", considered as the removal of blood stasis by traditional practitioners, will fade within a few days. Normally, this treatment is not considered as painful, but as relaxing and easing tense muscles.

In this study, the investigators will investigate the effectivity of Gua Sha massage in treating chronic neck pain. The investigators will research effects on subjective pain intensity, neck pain specific disability and haptic perception.

02

Conditions studied

  • Neck Pain

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Keywords

  • neck pain
  • massage
  • hyperthermia, induced
  • touch perception
  • randomized controlled trial
03

In context

Neck Pain

1,232 studies on the registry are indexed under Neck Pain; 255 are open to participants now.

This study's enrollment of 50 is close to the median of 52 across 1,004 interventional studies indexed under Neck Pain.

Browse Neck Pain studies →

Lead sponsor

Universität Duisburg-Essen is the lead sponsor of 82 studies on the registry; 13 are open to participants now.

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

04

Who can participate

Ages eligible
18 Years to 75 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Chronic mechanical neck pain, at least 40 mm on a 100mm visual analog scale.
  • Pain for at least 3 months.

Exclusion criteria

Exclusion Criteria:

  • radicular symptoms
  • congenital spine deformity
  • pregnancy
  • rheumatic diseases
  • oncologic diseases
  • other severe psychiatric or somatic comorbidity
  • recent invasive or surgical treatment of the spine
  • participation in other studies
  • skin diseases in the area to be treated
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
50 participants (actual)

Study arms

  • Active comparator
    Gua Sha

    Single Gua Sha treatment of the neck and shoulder region.

    Other: Gua Sha

  • Active comparator
    Thermotherapy

    Single use of a mud heat pad on the neck and shoulder region.

    Device: Thermotherapy

Interventions

  • OtherGua Sha

    Single Gua Sha treatment of the neck and shoulder region

  • DeviceThermotherapy

    Single use of a mud heat pad on the neck and shoulder region

06

What researchers measure

Primary outcomes

  1. Neck pain intensity (100mm visual analog scale)

    Time frame: Day 4

Secondary outcomes

  1. Neck disability index (NDI)

    The Neck Disability Index is an instrument to assess neck pain complaints. Reference: Vernon H, Mior S. The Neck Disability Index: a study of reliability and validity. J Manipulative Physiol Ther 1991;14:409-415.

    Time frame: Day 4

  2. Haptic perception

    The design consists of two angle legs, of which one angle leg has to be readjusted to a given angle adjustment. This is done by haptic perception without visual feedback. The deviation of the adjusted angle from the locked angle is measured. Reference: Grunwald, M., Ettich, C., Busse, F., Assmann, B., Dähne, A., Gertz, H.-J., (2002): Angle paradigm: A new method to measure right parietal dysfunctions in anorexia nervosa. Archives of Clinical Neuropsychology , 17, pp. 485- 496

    Time frame: Day 4

07

Study locations

1 site
  • Kliniken Essen-Mitte, Knappschafts-Krankenhaus, Department for Internal and Integrative Medicine
    Essen, Northrhine-Westphalia 45276, Germany
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 23, 2011, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01233180
Lead sponsor
Universität Duisburg-Essen
First posted
Nov 3, 2010
Start date
Sep 2010
Primary completion
Feb 2011
Completion
Feb 2011
Last update
Feb 23, 2011

Oversight

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

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This study is completed, as verified in Feb 2011. You cannot join it, but the record below documents what was studied.

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