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The Effect of Instrument Assisted Soft Tissue Mobilization in Female Patients With Myofascial Pain Syndrome

K

Kirsehir Ahi Evran Universitesi

Status

Completed

Conditions

Instrument Assisted Soft Tissue Mobilization
Myofascial Pain

Treatments

Other: Instrument Assisted Soft Tissue Mobilization
Other: Home exercises programe
Other: Sham Instrument Assisted Soft Tissue Mobilization

Study type

Interventional

Funder types

Other

Identifiers

NCT05297656
Local ethics (Other Identifier)
E-77504701-604.02.-00000386201

Details and patient eligibility

About

The primer aim of this study is to demonstrate the effecti of instrument assisted soft tissue mobilization on pain, functionality, quality of life and depression in the treatment of female patients with myofascial pain syndrome due to active trigger points in the upper trapezius muscles

Full description

Myofascial Pain Syndrome (MAS); It is a non-articular, non-inflammatory regional musculoskeletal pain syndrome characterized by myofascial trigger points located at muscle, fascia or tendon insertion sites and the spread of pain to reference areas by palpation of these points.

h The effectiveness of massage therapy in MAS is known. In this study, investigators will apply instrument assisted deep tissue mobilization (graston massage). Instrument-assisted soft tissue mobilization massage, which is a type of massage, will be applied by a physiotherapist who has a certificate on this subject and takes part as an assistant researcher in our study.

Soft tissue mobilization is a unique soft tissue mobilization combined with active mobility and stretching exercises already prescribed for patients with musculoskeletal injuries.

The various sizes and beveled edges of the stainless steel instruments allow physiotherapists to tailor treatment to different muscle structures facing myofascial constraints.

Localized increases in blood flow and soft tissue realignment lead to muscle function, increased normal joint motion, and decreased pain.

It has been investigated in the literature for many different diseases (trigger finger, nonspecific low back pain, myofascial pain syndrome) and found to be effective.CF

Enrollment

75 patients

Sex

Female

Ages

18 to 45 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Being woman and between the ages of 18-45
  2. Not to be in menopause
  3. Pain in the upper trapezius area
  4. Detection of a taut band in the upper trapezius region on examination
  5. At least one active trigger point in the tension band in the upper trapezius region on examination
  6. The pain caused by the compression of the trigger point is the pain that the patient complains about
  7. Painful restriction of cervical lateral flexion motion during stretching
  8. Pain 4 or more according to NRS

Exclusion criteria

  1. major surgery or trauma to the musculoskeletal system, especially the spine and upper extremities 2.History of any operation related to the head and neck region 3. Neuromuscular disease 4. History of rheumatic disease, malgnite in the active period 4. Cervical discopathy, cervical spondylosis, pathologies related to the shoulder joint and surrounding soft tissues, scoliosis, kyphosis, leg length difference, polio sequelae, developmental hip dysplasia 5. Psychiatric disease (Beck Depression Inventory score of 30 and above) 6.Obese (BMI≥30 kg/m2)

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

75 participants in 3 patient groups

Experimental Group
Experimental group
Description:
A total of 8 sessions of graston massage protocol will be applied to the patients in the experimental group for 4 weeks, 2 days a week for 5 minutes, at the hospital operating within the body of Kırşehir Ahi Evran University Physical Therapy and Rehabilitation Center. All patients will also receive home exercise therapy including stretching of the trapezius muscle and posture exercises
Treatment:
Other: Instrument Assisted Soft Tissue Mobilization
Other: Home exercises programe
Sham Comparator Group
Sham Comparator group
Description:
A total of 8 sessions of sham graston massage protocol will be applied to the patients in the experimental group for 4 weeks, 2 days a week for 5 minutes, at the hospital operating within the body of Kırşehir Ahi Evran University Physical Therapy and Rehabilitation Center. Sham graston massage is not a deep tissue massage, but will be performed with the device superficially, without applying pressure and mobilization. All patients will also receive home exercises.
Treatment:
Other: Sham Instrument Assisted Soft Tissue Mobilization
Other: Home exercises programe
Control group
Other group
Description:
The volunteers in the control group will be only given home exercise therapy including stretching of the trapezius muscle and posture exercises
Treatment:
Other: Home exercises programe

Trial contacts and locations

1

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Central trial contact

Basak Cigdem Karacay, Asst Prof

Data sourced from clinicaltrials.gov

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