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Comparison the effects of 5-week myofascial self-release and massage therapy in women with myofascial pain syndrome of Trapezius muscle: clinical trials

Comparison the effects of 5-week myofascial self-release and massage therapy in women with myofascial pain syndrome of Trapezius muscle: clinical trials

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20230914059432N1
Enrollment
45
Registered
2024-03-29
Start date
2023-09-29
Completion date
Unknown
Last updated
2024-05-27

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

Conditions

myofascial pain syndrome. Other chronic pain

Interventions

Intervention 1: The first intervention group: myofascial release massage for 2 days a week with variable times (gradual increase each week) for 5 weeks in which Swedish massage techniques will be used

Sponsors

Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 30 Years

Inclusion criteria

Inclusion criteria: Having active trigger points in the trapezius muscle Not using an exercise program or any other modalities which can effects persons pain experience caused by trigger points during the research period. Female gender Absence of pregnancy induvial must not any history of surgery or disorder in the cervical and thoracic spine Not having skin diseases and open wounds Not having an allergy to massage oils The minimum age is 20 and the maximum is 30

Exclusion criteria

Exclusion criteria: Use of alcohol and other drugs Not participating in massage sessions or training for two consecutive sessions Dissatisfaction with the continuation of the activity and cooperation in the current research Absence of individual during the pre-test and post-test session

Design outcomes

Primary

MeasureTime frame
Trigger points pain. Timepoint: Pain measurement will be done at the beginning of the study during the pre-test stage and at the end of the study in the post-test stage. Method of measurement: Using The visual analog scale (VAS) and The Brief Pain Inventory (BPI).;Neck range of motion in flexion, extension, rotation, and lateral flexion movements. Timepoint: Range of motion measurement will be done at the beginning of the study during the pre-test stage and at the end of the study in the post-test stage. Method of measurement: Using Goniometer.;Shoulder range of motion in flexion, extension, abduction, internal and external rotation. Timepoint: Range of motion measurement will be done at the beginning of the study during the pre-test stage and at the end of the study in the post-test stage. Method of measurement: Using Goniometer.;Hand and shoulder performance quality. Timepoint: Hand and shoulder performance quality will be measured at the beginning of the study during the pre-test stage and at the end of the study in the post-test stage. Method of measurement: The disabilities of the arm, shoulder and hand (DASH) questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSara Matinfard

Shahid Beheshti University Faculty of Sports Sciences and Health

s.matinfard@sbu.ac.ir+98 51 4222 6487

Outcome results

None listed

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