Treatment of Pectoralis Trigger Points in Patients With Pseudo Angina (GT-LIC)
2026年7月22日 更新者:Muhammad Muneeb Jafar、University of Faisalabad
Comparative Effects of Graston Technique Versus Local Ischemic Compression on Trigger Points of Pectoralis Major and Minor Among Pseudo-angina Patients
Pseudo-angina is a musculoskeletal condition characterized by chest pain that resembles angina but occurs due to non-cardiac causes, particularly myofascial trigger points in the chest wall muscles.
Trigger points in the pectoralis major and minor muscles may contribute to pain, discomfort, and functional limitations by affecting muscle activity and movement.
Manual therapy techniques such as the Graston Technique and Local Ischemic Compression (LIC) are commonly used to manage soft tissue dysfunction and myofascial trigger points.
This study aims to compare the effects of the Graston Technique and Local Ischemic Compression on pain reduction and functional improvement in patients with pseudo-angina.
調査の概要
状態
まだ募集していません
詳細な説明
This is Multiple-center, randomized controlled trail.
Participants age 25-50 years with diagnosed pseudo angina will be referred from cardiology department of Aziz Fatima and Faisal hospital to Madina Teaching hospital (MTH) Physiotherapy ward and Jafar Physiotherapy Clinic.
After informed consent Participants will be randomly assign to one of two parallel groups using a random number generator.
Group A (Experimental): Receive Graston technique 3 sessions per week for total duration 4 weeks.
Group B (Active Comparator) receive the LIC 3 sessions per week for total duration 4 weeks.
Outcome measures (pain via NPRS, Shoulder Pain and Disability Index (SPADI)) are taken at baseline and end of treatment.
Data will be analyzed using Spss version 20.
研究の種類
介入
入学 (推定)
36
段階
- 適用できない
連絡先と場所
このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。
研究連絡先
- 名前:Dr. Muhammad Muneeb Jafar, PhD Physical therapy
- 電話番号:+923127000616
- メール:muneebjafar.DPT@tuf.edu.pk
研究連絡先のバックアップ
- 名前:Dr Maryam Farooq, Phd Physical therapy
- 電話番号:+923326760155
- メール:Maryamfarooq2527@gmail.com
研究場所
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Punjab Province
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Faisalābad、Punjab Province、パキスタン、38000
- The University of Faisalabad
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参加基準
研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。
適格基準
就学可能な年齢
- 大人
健康ボランティアの受け入れ
いいえ
説明
Inclusion Criteria:
- Participants which fulfill the Simon's Trigger Point Diagnostic Criteria
- Referred by Cardiologist • Patients with Trigger Points in chest Muscles and left Pectoralis Major and Minor muscles.
Exclusion Criteria:
- Spinal Deformity • Gastric Problems • Any cardiac disease • Heart Burns • Panic Attacks • Pleurisy • Pulmonary Embolism • Pericarditis.
研究計画
このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。
研究はどのように設計されていますか?
デザインの詳細
- 主な目的:処理
- 割り当て:ランダム化
- 介入モデル:並列代入
- マスキング:ダブル
武器と介入
参加者グループ / アーム |
介入・治療 |
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実験的:Graston Technique
articipants assigned to this arm received the Graston Technique, an instrument-assisted soft tissue mobilization intervention, applied to the identified myofascial trigger points of the pectoralis major and pectoralis minor muscles.
The intervention was performed after a gentle Z-stretch of the targeted muscles as baseline treatment.
A stainless-steel Graston instrument was applied using controlled strokes at approximately a 45° angle to the skin surface, following the direction of the muscle fibers and across the fibers to mobilize soft tissue restrictions.
The treatment was applied for approximately 40-120 seconds over each targeted area.
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A stainless-steel Graston instrument was applied using controlled strokes at approximately a 45° angle to the skin surface, following the direction of the muscle fibers and across the fibers to mobilize soft tissue restrictions.
The treatment was applied for approximately 40-120 seconds over each targeted area.
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実験的:Local Ischemic Compression
Participants assigned to this arm received LIC applied to the identified myofascial trigger points of the pectoralis major and pectoralis minor muscles.
Following a gentle Z-stretch of the targeted muscles as baseline treatment, sustained manual pressure was applied gradually over each trigger point until a tolerable level of discomfort was achieved.
The compression was maintained for approximately 90 seconds per trigger point and repeated 1-3 times during each treatment session according to patient tolerance and clinical response.
The technique was performed using the therapist's thumb, finger, or knuckle depending on the location and depth of the trigger point.
Participants received four physiotherapy sessions over a two-week period, with sessions conducted on alternate days.
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Sustained manual pressure was applied gradually over each trigger point until a tolerable level of discomfort was achieved.
The compression was maintained for approximately 90 seconds per trigger point and repeated 1-3 times during each treatment session according to patient tolerance and clinical response.
The technique was performed using the therapist's thumb, finger, or knuckle depending on the location and depth of the trigger point
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この研究は何を測定していますか?
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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Shoulder Pain Disability Index
時間枠:Baseline and 4 week post intervention
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The Shoulder Pain and Disability Index is a well-known neutral measure for assessing the level of pain and functional impairment experienced by people with shoulder issues.
It is frequently used in clinical and research settings to assess the severity of shoulder problems and track therapy efficacy.
It consists of 13 elements organized into two subscales.
The Pain Subscale consists of five items that determine how intense pain is in various circumstances, such as at rest or during activities.
The disability subscale consists of eight items: it assesses the level of difficulty with specific everyday shoulder-related tasks, such as lifting weights or putting on a shir
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Baseline and 4 week post intervention
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Numeric Pain Rating Scale
時間枠:Baseline and 4 week post intervention
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NPRS was used as a primary outcome measure to evaluate pain intensity in patients with pseudo-angina.
On the scale, 0 represents no discomfort and 10 represents severe pain.
At rest and while engaging in activities, participants were asked to rate their level of pain.
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Baseline and 4 week post intervention
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ここでは、この調査に関係する人々や組織を見つけることができます。
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出版物と役立つリンク
研究に関する情報を入力する責任者は、自発的にこれらの出版物を提供します。これらは、研究に関連するあらゆるものに関するものである可能性があります。
一般刊行物
- This citation will not be hyperlinked on ClinicalTrials.gov. The effectiveness of instrument- assisted soft tissue mobilization technique (ergonš technique), cupping and ischaemic pressure techniques in the treatment of amateur athletes΄ myofascial trigger points. Journal of Novel Physiotherapy S (3): 1-7.
- This citation wilnot be hyperlinked on ClinicalTrails.gov. Fousekis K, Kounavi E and Doriadis S (2016) The Effectiveness of instrument- assisted soft tissue mobilization technique, cupping and ischemic pressure techniques in the treatment of amateur athlete's myofascial trigger points. Journal of Novel Physiotherapies 3(2): 1-7.
研究記録日
これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。
主要日程の研究
研究開始 (推定)
2026年7月25日
一次修了 (推定)
2026年10月1日
研究の完了 (推定)
2026年11月1日
試験登録日
最初に提出
2026年7月22日
QC基準を満たした最初の提出物
2026年7月22日
最初の投稿 (実際)
2026年7月27日
学習記録の更新
投稿された最後の更新 (実際)
2026年7月27日
QC基準を満たした最後の更新が送信されました
2026年7月22日
最終確認日
2026年7月1日
詳しくは
本研究に関する用語
キーワード
その他の研究ID番号
- TUF/EIRB/136/2025
個々の参加者データ (IPD) の計画
個々の参加者データ (IPD) を共有する予定はありますか?
いいえ
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米国FDA規制医薬品の研究
いいえ
米国FDA規制機器製品の研究
いいえ
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