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Comparison between the effectiveness of laser therapy and graston technique on trigger points of upper trapezius

Comparison between the effectiveness of laser therapy and graston technique on trigger points of upper trapezius

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20210809052129N1
Enrollment
30
Registered
2021-10-08
Start date
2021-07-05
Completion date
Unknown
Last updated
2021-11-01

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

Conditions

Myofascial pain syndrome. Chronic widespread pain

Interventions

Intervention 1: Intervention group 1: Graston therapy. Graston tool is used for 1 minute sweeping of upper trapezius, 2 minute swiveling and fanning of Trps then 1 minute swiveling of upper trapezius.

Sponsors

The University of Faisalabad
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: Females aged 18 to 50 years old with bilateral myofascial pain syndrome of the upper trapezius muscle. As stated by Simon’s diagnostic criteria, following sings should be present: Five majors: 1. Pain in a region 2. Pain referring to another area 3. A tight muscle band 4. A tender/painful location in the tight muscle band 5. Limited ROM. One minor: 1. Pain that can be regenerated by applying pressure on the location of the tender area 2. A local twitch response in the affected area 3. With prolonged neck and/or shoulder region pain, pain relief that can be achieved with injection or stretching. Complaint of pain from at least 8 weeks. Pain score between 30mm to 80mm on VAS. Neck extension range up to 30 degrees. Neck right and left side flexion range up to 20 degrees. NDI score between 10 and 24

Exclusion criteria

Exclusion criteria: Neck or shoulder pain that has lasted less than 8 weeks Within the previous three months, local injectable physiotherapy Infection Febrile state Cervical radiculopathy symptoms Hypertension that has not been treated Coagulatory disease or anticoagulant therapy Injury to the cervical spine or surgery Implants and metal devices

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: before intervention and after 2nd, 5th intervention session and then after 5 days of 5th session. Method of measurement: Pain measurement by visual analogue scale.;Neck disability Index. Timepoint: before intervention and after 2nd, 5th intervention session and then after 5 days of 5th session. Method of measurement: Neck functioning measurement by neck disability index.

Secondary

MeasureTime frame
(1) Cervical extension ROM. Timepoint: before intervention and after 2nd, 5th intervention session and then after 5 days of 5th session. Method of measurement: Ranges of motion are measured by goniometry.;Cervical right lateral flexion ROM. Timepoint: before intervention and after 2nd, 5th intervention session and then after 5 days of 5th session. Method of measurement: Ranges of motion are measured by goniometry.;Cervical left lateral flexion ROM. Timepoint: before intervention and after 2nd, 5th intervention session and then after 5 days of 5th session. Method of measurement: Ranges of motion are measured by goniometry.

Countries

Pakistan

Contacts

Public ContactSaba Iqbal

The University of Faisalabad

sabaiqbal71263@gmail.com+92 41 2646649

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026