Effect of Cervical Stability Training on Somatosensory Evoked Potential and Cervical Spine in Forward Head Posture (FHP)
調査の概要
詳細な説明
The use of electronic tools is increasing in worldwide varieties and the attractiveness of these tools lead to variety of groups of people, especially teenagers, using them for prolonged period of time leading to increased musculoskeletal problems. Excessive use of smartphones for long period of time can lead to decreased postural control and forward head postur (FHP) as phone users maintain an abnormal alignment of the head and neck. The habit of repetitive use of computers, TV, mobile phones, and video games and even back packs forces the body to exhibit bad posture. The overall prevalence of FHP was reported to be 66% in computer based workers.
cervical stability training play a major role in treatment of forward head posture so this study will be conducted to investigate its role on craniovertebral angle, cervical range of motion, pain intensity level, functional disability, neck flexor and extensor muscles endurance, lordotic cervical curvature, somatosensory evoked potential in forward head patient.
研究の種類
入学 (予想される)
段階
- 適用できない
連絡先と場所
研究連絡先
- 名前：salah E Ahmed, master
- 電話番号：01158125773
- メール：salaheid07@gmail.com
研究場所
-
-
-
Giza、エジプト、11251
- Salah Eid Ahmed Ali
-
-
参加基準
適格基準
就学可能な年齢
健康ボランティアの受け入れ
受講資格のある性別
説明
Inclusion Criteria:
Adult participant (18-to-40years old) with forward head posture, BMI 20-to-25 kg/m², The area of mechanical neck pain will defined to the cervical region, possibly with referred pain into the occipit, nuchal muscles, and shoulders, All patients will have chronic neck pain for more than 3 months, Craniovertebral angle of ˂ 49.
Exclusion Criteria:
Signs of serious pathology (e.g., rheumatoid diseases, ankylosing spondylitis), History of cervical spine surgery, History of trauma or fractures in cervical spine, Signs of cervical radiculopathy or myelopathy, Vascular syndrome such as vertebrobasilar insufficiency.
研究計画
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 |
|---|---|
|
実験的：cervical stability training
cervical stability training will be received three times a week for eight weeks
|
cervical stability training will be contain three phases, each phase has six positions ( supine, forearms, sidelying, four point kneeling, sitting and standing position)
TENS, hot packs, stretching exercise of superficial neck muscles, and postural advice.
|
|
アクティブコンパレータ：traditional treatment
traditional treatment will be received three times a week for eight weeks
|
TENS, hot packs, stretching exercise of superficial neck muscles, and postural advice.
|
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 |
|---|---|---|
|
somatosensory evoked potential
時間枠：up to eight weeks
|
somatosensory evoked potential will be measured by electromyograph device
|
up to eight weeks
|
|
craniovertebral angle
時間枠：up to eight weeks
|
craniovertebral angle will be measured photographically by surgimap program
|
up to eight weeks
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
pain intensity level
時間枠：up to eight weeks
|
pain will be measured by visual analogue scale
|
up to eight weeks
|
|
functional disability
時間枠：up to eight weeks
|
disability will be measured by arabic neck disability index
|
up to eight weeks
|
|
cervical range of motion
時間枠：up to eight weeks
|
Phone application (clinometer) will used to measure cervical range of motion using smartphone (Infinix Note 5)
|
up to eight weeks
|
|
endurance test
時間枠：up to eight weeks
|
flexion and extension endurance will be measured using pressure biofeedback unit
|
up to eight weeks
|
|
cervical curvature
時間枠：up to eight weeks
|
digital x ray will be used to measure cervical curvature
|
up to eight weeks
|
協力者と研究者
スポンサー
研究記録日
主要日程の研究
研究開始 (予想される)
一次修了 (予想される)
研究の完了 (予想される)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (実際)
学習記録の更新
投稿された最後の更新 (実際)
QC基準を満たした最後の更新が送信されました
最終確認日
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
- P.T.REC/012/003459
医薬品およびデバイス情報、研究文書
米国FDA規制医薬品の研究
米国FDA規制機器製品の研究
この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。