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A Study to Determine the Tissue Properties, Vascular Physiology and Biochemical Milieu of Myofascial Trigger Points

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상태완료
스폰서
George Mason University
협력자
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)

키워드

요약

Determine the effect of dry needling using a 32 gauge needle on active trigger points in subjects with chronic myofascial pain.
Participants will receive treatment for active trigger points (3 on successive weeks) and will have pain, status of the trigger point and functional measures assessed at baseline, after treatment and eight weeks later.

기술

Chronic myofascial pain syndromes, such as pain associated with myofascial trigger points (MTrPs), are prevalent yet poorly understood. Our long-term goal is to determine the pathogenesis and pathophysiological mechanisms of chronic pain associated with trigger points, eventually leading to the development of objective diagnostic criteria and effective pain management strategies. We propose to achieve this goal using a new and unique integrative methodology combining microanalytic biochemical assays, ultrasound technology (imaging) and mathematical modeling. An additional component of the study plan is to learn if a standard treatment for MTrPs is associated with the biochemical and ultrasound changes we will be measuring This project has the following specific aims: 1) To understand the viscoelastic soft tissue neighborhood and vascular physiology of affected muscle at a macroscopic level using ultrasound imaging, elastography and Doppler blood flow imaging; 2) To understand the pathophysiology of myofascial trigger points at a nanotechnological level through assays of biochemical milieu using a microdialysis technique; 3) To develop mathematical models of underlying pathophysiological mechanisms based on experimental observations for quantitative hypothesis testing; 4) To determine if dry needle therapy, a standard of care for MTrPs, changes the macroscopic and/or microscopic measurements and leads to resolution of the trigger point and secondarily associated pain symptoms.. Our hypothesis is that pathogenesis of myofascial pain syndrome involves local trauma to the muscle fibers, and the biochemical response to the injury leads to sustained muscle contracture, compression of blood vessels and a local energy crisis that causes tissue hypoxia and the expression of pain-producing substances at myofascial trigger points. Relieving the trigger point through dry needle therapy

날짜

마지막 확인: 07/31/2019
처음 제출: 06/09/2016
제출 된 예상 등록: 08/01/2019
처음 게시 됨: 08/04/2019
제출 된 마지막 업데이트: 08/01/2019
마지막 업데이트 게시: 08/04/2019
실제 연구 시작 날짜: 07/31/2010
예상 기본 완료 날짜: 02/29/2016
예상 연구 완료 날짜: 02/29/2016

상태 또는 질병

Myofascial Pain

개입 / 치료

Procedure: SIngle arm

단계

-

팔 그룹

개입 / 치료
Other: SIngle arm
Single arm, intervention All recipients were treated with dry needling technique into active myofascial trigger points They received 1 treatment weekly for three weeks.
Procedure: SIngle arm
insertion of needle into active myofascial trigger point

자격 기준

공부할 수있는 연령 18 Years 에 18 Years
공부할 수있는 성별All
건강한 자원 봉사자를 받아들입니다
기준

Inclusion Criteria:

- spontaneous soft tissue pain in shoulder and neck region

Exclusion Criteria:

- recent fracture, neurological injury or history of stroke, use of opioids

결과

1 차 결과 측정

1. Verbal Analog Scale [change from baseline to 3 weeks and at 8 weeks]

scale of 0-10 as a measure of pain severity

2. Presence of myofascial trigger point [change from baseline to 3 weeks and at 8 weeks]

Digital palpation of the trigger point was performed by investigators and scored as present or absent; if present was it associated with spontaneous pain or was pain induced with palpation

3. Brief Pain Inventory [change from baseline to 3 weeks and at 8 weeks]

Validated scale of pain severity and interference

2 차 결과 측정

1. Oswestry Disability Scale [change from baseline to 3 weeks and at 8 weeks]

self-reports of disability

2. MOS-short form 36 v2 [change from baseline to 3 weeks and at 8 weeks]

self-reports of disability and health related quality of life Profile of Mood States, range of motion of neck and shoulder, manual muscle test)

3. Manual Muscle test [change from baseline to 3 weeks and at 8 weeks]

grade strength 0-5, neck and shoulder girdle muscle

4. Profile of Mood States [change from baseline to 3 weeks and at 8 weeks]

measures of mood and affect (depression and anxiety)

5. range of motion [change from baseline to 3 weeks and at 8 weeks]

shoulder and neck range of motion in degrees

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