- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT07692126
Core Stability vs Scapular Stabilization on Hand Grip Strength in Chronic Myofascial Neck Pain
Core Stability Exercises Versus Scapular Stabilization Exercises on Hand Grip Strength in Patients With Chronic Myofascial Neck Pain
연구 개요
상태
정황
상세 설명
연구 유형
등록 (추정된)
단계
- 해당 없음
연락처 및 위치
연구 연락처
- 이름: Adnan AA Gharib, PHD
- 전화번호: +201065798861
- 이메일: dradnanpts@gmail.com
연구 연락처 백업
- 이름: Magda Ramadan Zahran, Assistant Professor
- 전화번호: 01065798861
- 이메일: dradnanpts@gmail.com
연구 장소
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Giza Governorate
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Giza, Giza Governorate, 이집트, 11432
- 모병
- Cairo University
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연락하다:
- Magda Ramadan Zahran, Assistant Professor
- 전화번호: 01065798861
- 이메일: dradnanpts@gmail.com
-
연락하다:
- Adnan AA Gharib, PHD
- 전화번호: 01065798861
- 이메일: dradnanpts@gmail.com
-
수석 연구원:
- Adnan AA Gharib, PHD
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참여기준
자격 기준
공부할 수 있는 나이
- 성인
건강한 자원 봉사자를 받아들입니다
설명
Inclusion Criteria:
- Patients diagnosed with chronic myofascial neck pain depending on referral, and physical examination.
- Sixty patients diagnosed with chronic myofascial neck pain for more than six months.
- Patients age range will 25-45 years
- Patients body mass index (BMI) will be 18.5-24.9 kg/m2
- Each patient suffering from all active MTrPs in the upper trapezius muscle with painful/ tender nodule.
- Patients have a constant neck pain with positive jump sign when palpating the upper trapezius muscle.
- Patients have referred pain, and symptoms of ipsilateral hand muscle weakness.
- No history of undergoing physiotherapy modalities or corticosteroid injection therapies in the past six months before the study
Exclusion Criteria:
- Presence of signs of severe pathology such as malignancies, mainly of the cervical region.
- Fracture of the cervical spine.
- Cervical radiculopathy or myelopathy.
- Diabetes mellitus.
- Trauma, cognitive anomalies, and surgery around neck, shoulders, or hand.
- Fibromyalgia or vascular syndromes such as vertebral basilar insufficiency.
- Pregnancy.
- Having undergone physical therapy within the past three months before the study.
- Having corticosteroid injection therapies in the past 3 months before the study.
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 치료
- 할당: 무작위
- 중재 모델: 병렬 할당
- 마스킹: 네 배로
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
|---|---|
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실험적: Experimental Group A (Core Stability)
consists of 20 participants who receive core stability exercises, plus the traditional physical therapy program in the form of ischemic compression of upper trapezius muscle, strain-counter strain of upper trapezius muscle, and muscle energy technique of upper trapezius muscle, three sessions per week for 6 weeks.
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The core stability exercise protocol will be conducted to experimental group (A), only. The core stability exercise protocol will be conducted for 40-45 minutes (10 minutes worm-up 'stretch exercises', 25 minutes core stabilization exercises, and 5-10 minutes cool down exercises 'stretch exercises') 3 sections/ week for six weeks 1. Diaphragm Core '';360 degree expansion breathing, weighted breathing 2. Transverse abdominis 'Abdominal drawing in maneuver, supine vacuum, pelvic tilt'; 3. Multifidus 'quadruped altered leg/arm, bridge with leg extension'; 4. Pelvic Floor muscles/Kegel, bridging, and bridging dog, and squat Core stability exercise.
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실험적: Experimental Group B (Scapular Stabilization)
consists of 20 participants who receive scapular stabilization exercise, plus the traditional physical therapy program, three sessions per week for 6 weeks.
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The scapular stabilization exercise protocol will be conducted to experimental group (B), only. The core scapular stabilization exercise protocol will be conducted for 40-45 minutes (10 minutes worm-up 'stretch exercises', 25 minutes scapular stabilization exercises, and 5-10 minutes cool down exercises 'stretch exercises') 3 sections/ week for six weeks a. Open chain stabilization exercises 'scapular elevation/depression, upward/downward rotation', b. Static closed chain stabilization exercises 'Protected weight bearing through both hands leaning against wall', c. Dynamic closed chain stabilization exercises 'scapular retraction' |
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활성 비교기: Control Group C (Traditional Physical Therapy Program)
consists of 20 participants who receive the traditional physical therapy program, three sessions per week for 6 weeks, only
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연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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Hand Grip Strength
기간: 1. At Baseline (Pre-procedure), 2. Post-treatment (Post 6 weeks of treatment program).
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Hand-held Dynamometer (SAMMONS PRESTON, INC.
Bolingbrook, IL604404989) will be used to measure it.
The patient will sit on a standard height chair with no armrest with his/ her forearm in a neutral position, and shoulder in adducted and neutral rotation, with elbow flexed 90 degrees (°).
The patient will be requested to squeeze the ipsilateral hand on the hand grip dynamometer handle accordingly to the ordered verbs 'i.e., one, two, three, squeeze…harder, harder'.
Three measures will be conducted with one minute a break in between, then the average will be recorded in value score.
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1. At Baseline (Pre-procedure), 2. Post-treatment (Post 6 weeks of treatment program).
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Pinch Grip Strength
기간: 1. At Baseline (Pre-procedure), 2. Post-treatment (Post 6 weeks of treatment program).
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The pinch gauge (FEI, White plains, NY 10602, USA) will be used to measure the pinch grip strength, it is a valid and reliable tool.
The patient will sit on a standard height chair with no armrest with his/ her shoulder, elbow, forearm, and wrist in a neutral position.
The patient will be requested to squeeze the thumb pad as firm as possible against the lateral aspect of index fingers' middle phalanx, while the examiner will hold the distal end of the pinch gauge.
Three measures will be conducted with one minute a break in between, then the average will be recorded in a score value.
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1. At Baseline (Pre-procedure), 2. Post-treatment (Post 6 weeks of treatment program).
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2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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Chronic Myofascial Neck Pain Intensity assessment using Numerical Pain Rating Scale:
기간: 1. At Baseline (Pre-procedure), 2. Post-treatment (Post 6 weeks of treatment program).
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Numerical Pain Rating Scale will be used to assess chronic myofascial neck pain intensity, The patient will be in a relaxed position then will be given the appendix which contains numerical pain rating scale.
It involves a 0-10 scale, where 0 represents "no pain" and 10 represents "the worst pain imaginable" The patient will be instructed to place a vertical mark on the line to indicate his/her pain.
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1. At Baseline (Pre-procedure), 2. Post-treatment (Post 6 weeks of treatment program).
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Pressure Pain Threshold using electronic pressure algometer
기간: 1. At Baseline (Pre-procedure), 2. Post-treatment (Post 6 weeks of treatment program).
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The electronic pressure algometer 'force one gauge model FDI' (Wagner instruments, Greenwash, CT, USA) will be used to measure it, it is a valid and reliable tool.
Over trigger point recognized via jump sign clinically, a dial-style pressure algometry will be installed while a steady vertical pressure will be applied.
When the patient reported only mild pain, the patient will be asked to raise hand to indicate it.
Three measures will be conducted with one minute a break in between, then average will be recorded in value.
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1. At Baseline (Pre-procedure), 2. Post-treatment (Post 6 weeks of treatment program).
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Whole Upper Extremity Functional Level using Arabic-Q-DASH scale
기간: 1. At Baseline (Pre-procedure), 2. Post-treatment (Post 6 weeks of treatment program).
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The whole upper extremity functional level will be evaluated using Arabic-Q-DASH it is a valid and reliable tool.
The Arabic-Q-DASH is like the original questionnaire.
Items have a rating scale ranged from 1 to 5. The patient will be instructed to place a score that the examiner will transform it into a value between 0 and 100.
The high score indicates better hand function outcomes with exception of pain, where high value indicates more intense pain score.
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1. At Baseline (Pre-procedure), 2. Post-treatment (Post 6 weeks of treatment program).
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공동 작업자 및 조사자
스폰서
수사관
- 연구 책임자: Sohair Shehata Rezkallah, Professor, Cairo University; Faculty of Physical Therapy
연구 기록 날짜
연구 주요 날짜
연구 시작 (실제)
기본 완료 (추정된)
연구 완료 (추정된)
연구 등록 날짜
최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (실제)
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
추가 정보
이 연구와 관련된 용어
키워드
기타 연구 ID 번호
- P.T.REC/012/006550
개별 참가자 데이터(IPD) 계획
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