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Neck PainNaSKNCT01500330

Home Use of Cupping Massage in Chronic Neck Pain

A study testing cupping massage and Progressive muscle relaxation in people with Neck Pain, run by Universität Duisburg-Essen at 1 site in Germany.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The purpose of this randomized controlled study is to determine the effectiveness of cupping massage as home use for patients with chronic nonspecific neck pain compared to relaxation exercise. Read more about this study

Who is it for?
Ages 18 to 75 years
Conditions the study is for
Neck Pain
What is being tested?
cupping massage and Progressive muscle relaxation
Type of treatment
Surgery or procedure
Could I receive a placebo?
No, everyone receives an active treatment
How many people
84 participants
Where
1 siteGermany
Study dates
Jan 2012to May 2012
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 75 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • mean neck pain intensity 45mm
  • neck pain for at least 3 months
  • age 18-75
  • partner or friend for the application of the massage

Who cannot join

  • specific neck pain due to trauma, neurological disorder, prolapse, operation, cancer
  • severe deformity of the spine
  • skin disease, allergy on the neck area
  • hemophilia, anticoagulation, antiplatelet disorder
  • severe psychiatric disorder
  • severe comorbidity
Show all 9Show fewer
  • regular intake of opiates and corticosteroids >10mg prednisolon
  • pregnancy
  • participation in other clinical trials

Trial locations and contacts

1 site in 1 country.

Germany1 site
  • Klinik für Naturheilkunde

    Essen

Other trials in Germany

About this study

Official title: Randomised Controlled Study on the Effectiveness of Cupping Massage for Home Use in Chronic Neck Pain [Randomisierte Kontrollierte Studie Zur Wirksamkeit Der Schröpfkopfmassage Als Heimanwendung Bei Chronischen Nackenschmerzen]

The purpose of this randomized controlled study is to determine the effectiveness of cupping massage as home use for patients with chronic nonspecific neck pain compared to relaxation exercise.

Read the detailed description

see above

Conditions
Neck Pain
Being tested
cupping massage, Progressive muscle relaxation
Medical subject headings
Neck Pain

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • cupping massageProcedure or surgery

    the upper back is covered in massage oil the cupping glass is drawn along the back muscles

  • Progressive muscle relaxationProcedure or surgery

    standardized programme on muscle relaxation according to Jacobson

Study groups in NCT01500330
Study groupRoleWhat they receive
cupping massageExperimental12 weeks home use of cupping massage (delivered by the partner or friend) twice a week for 20 minutes
Receives: Procedure: cupping massage
control groupActive comparatorprogressive muscle relaxation twice a week for 20 minutes
Receives: Procedure: Progressive muscle relaxation

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Pain Intensity

    Pain intensity on a 100mm visual analogue scale

    Measured: T2 (84 days)

Secondary outcomes (9)
  1. Pain diary

    Pain intensity on a visual analogue scale

    Measured: week 12

  2. pain intensity in motion

    Pain intensity induced by flexion, extension, lateral flexion and rotation of the head

    Measured: T2 (84 days)

  3. pain quality

    sensory and affective pain quality, questionnaire

    Measured: T2 (84 days)

  4. well being

    Well being measured by questionnaire (FEW16)

    Measured: T2 (84 days)

  5. Quality of life

    measured by the SF-36

    Measured: T2 (84 days)

  6. Stress perception

    Measured by the PSQ20

    Measured: T2 (84 days)

  7. Control belief

    measured by the GKÜ (questionnaire on control beliefs)

    Measured: T2 (84 days)

  8. Pressure pain threshold

    pressure pain threshold measured with an algometer on predefined muscles and the pain maximum

    Measured: T2 (84 days)

  9. Safety

    all adverse events are recorded

    Measured: T2(84 days)

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted28 Dec 2011 (estimated)
  2. Study startJan 2012
  3. Primary completionMay 2012
  4. Study completionMay 2012

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
84 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01500330
Sponsor's protocol ID
NaSK
Acronym
NaSK
Status last verified
Oct 2013
First submitted
22 Dec 2011
Last updated
9 Oct 2013
Results posted
No
Data monitoring committee
No

Publications

  • Lauche R, Materdey S, Cramer H, Haller H, Stange R, Dobos G, Rampp T. Effectiveness of home-based cupping massage compared to progressive muscle relaxation in patients with chronic neck pain--a randomized controlled trial. PLoS One. 2013 Jun 7;8(6):e65378. doi: 10.1371/journal.pone.0065378. Print 2013.

    PubMed 23762355

Questions about this trial

What is this clinical trial studying?

A study testing cupping massage and Progressive muscle relaxation in people with Neck Pain, run by Universität Duisburg-Essen at 1 site in Germany.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 9 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 9 Oct 2013. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Germany. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Pain Intensity (time frame: T2 (84 days)). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT01500330, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 9 Oct 2013; AzTrials last refreshed its copy on 7 Nov 2026.

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