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Effect of Dry Cupping and Ischemic Compression on the Trigger Point on the Upper Trapezius Muscle

Effect of Dry Cupping and Ischemic Compression on the Trigger Point on the Upper Trapezius Muscle

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05123105
Enrollment
25
Registered
2021-11-17
Start date
2021-01-23
Completion date
2021-03-30
Last updated
2021-11-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Trigger Point Pain, Myofascial

Keywords

ischemic compression, cupping, algometer, trapezius muscle

Brief summary

Ischemic compression is considered the fastest and most common method for providing relief in trigger point therapy, whereas cupping therapy is not a method often used for this purpose. The muscle that has a great impact on tension-type headaches and neck pain is the trapezius, whose upper fibres are where the most common trigger point in the back is located. The aim of this study was to evaluate and compare the effectiveness of single ischemic compression and single dry cupping therapy on the most common trigger point, on the descending part of the trapezius muscle.

Interventions

OTHER1) cupping therapy

The participant lay on his front on a couch. The examiner applied a plastic cup on a pre-marked trigger point, suctioned it with a mechanical pump and left it for 2 minutes. This was a stationary application with medium suction force. Therapy was performed on both sides. Measurements were taken before and 2 minutes after the therapy.

OTHER2) control test (no intervention)

The participant lay on his front on a couch for 4 minutes without any activity and without anyy intervention. Measurements were taken before and after the session.

OTHER3) ischemic compression

The participant lay on his front on a couch. The researcher applied pressure to a pre-marked trigger point using the thumb for 2 minutes until tissue resistance was felt. This included 60-second compression and after a break of a few seconds, another 60 seconds of compression. Therapies were performed on each side. Measurements were taken before and 2 minutes after the therapy.

Sponsors

Józef Piłsudski University of Physical Education
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Intervention model description

Each person participated in three tests with an interval of approximately one week between them. The following study protocol was followed; (short version) 1. cupping therapy; \- a minimum interval of 7 days; 2. control test; \- a minimum interval 7 days; 3. ischemic compression.

Eligibility

Sex/Gender
ALL
Age
18 Years to 30 Years
Healthy volunteers
Yes

Inclusion criteria

* age 18-30 * student of The Józef Piłsudski University of Physical Education in Warsaw * written consent to participate in the study

Exclusion criteria

* past or current injury to the trapezius. * past or current injury of the cervical spine limiting mobility of this segment. * broken skin at the examination site. * cardiological disease and use of blood pressure medication, histamine medication and analgesics * elevated body temperature, illness symptoms and a period of convalescence. * a missed anti-Covid procedure before each examination. * inability to find trigger points.

Design outcomes

Primary

MeasureTime frameDescription
Pain pressure threshold test (PPT)changes from baseline in pain pressure threshold at 2 minutes after the sessionThe trigger points of the upper section of the trapezius on the right and left sides were determined by palpation and were also indicated using a marker. A Wagner FDX 50 Force Gage algometer was applied to the trigger point. The pressure force was increased by 1kg/cm2/s until the patient felt pain, which was the pain pressure threshold (PPT) measured in kg/cm2. The test was performed on both sides. The test was performed twice on each side - before and 2 minutes after the session.
Cervical spine mobility testchanges from baseline in cervical spine mobility at 2 minutes after the sessionEach examination began in a sitting position with a cervical spine mobility test. The following bone points were marked on the participants' skin using a marker: spinous process of the 7th cervical vertebra, external occipital protuberance, the top of the chin, the jugular notch of the sternum, the mastoid of the temporal bone, and the acromion process of the scapula. Next, a linear measurement of the range of motion was performed using a tape measure to ascertain the distance between the marked points in the initial position and after the active movement for flexion (forward bending), extension (backward bending), lateral bending and rotation to both sides, respectively. The mobility was determined by the difference of the two measurements. The test for each movement (i.e. flexion (forward flexion), extension (backward flexion), lateral flexion and both sides rotation) was performed twice - before and 2 minutes after the session.

Secondary

MeasureTime frameDescription
HeightMeasurements were taken before the first sessionHeight measured in meters
WeightMeasurements were taken before the first sessionWeight measured in kilograms

Countries

Poland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026