Effects of Hip Hinge Exercises on Pain, Range of Motion and Functional Disability in Non-specific Low Back Pain.
the effects of hip hinge exercises in non-specific low back pain patients along with that we will measure the range of motion of lumbar region. Low back pain (LBP) is a prevalent musculoskeletal condition worldwide and a leading cause of disability, affecting individuals' physical functioning and quality of life.
調査の概要
状態
条件
研究の種類
入学 (推定)
段階
- 適用できない
連絡先と場所
研究連絡先
- 名前:Imran IMRAN Amjad, PHD
- 電話番号:9233224390125
- メール:imran.amjad@riphah.edu.pk
研究場所
-
-
Punjab Province
-
Lahore、Punjab Province、パキスタン、54000
- Al Shafi Hospital Lahore
-
-
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:
- age 18-60 years
- Both genders
- Diagnosed with chronic non-specific low back pain
- Pain intensity > 4 on NPRS on baseline
Exclusion Criteria:
- Specific causes of back pain (radiculopathy, spondylolisthesis, spinal stenosis, fracture, infection, malignancy)
- History of spinal surgery in past 12 months.
- Neurological deficits affecting safe exercise performance.
- Pregnancy or unstable medical conditions.
- Participation in other structured rehabilitation programs.
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:独身
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
|
実験的:Group A
For Group A 3 session per week within pain-free limits, progressing as tolerated and 45-60 minutes time per session. |
Functional drills focusing on hip flexion with neutral spine including body weight hip hinging with dowel feedback and progression as tolerated. Exercises will emphasize gluteus activation and eccentric protocol to minimize lumbar flexion. Spine bridges and clamshells to strengthen the Gluteus Maximus and Medius, addressing posterior chain weakness commonly seen in NSLBP. Active and static stretching for hip flexors and extensors in pain free range of motion. |
|
他の:Group B
For Group B 3 sessions per week within pain free range of motion as tolerated and session last for 45- 60 minutes per session |
Core stabilization exercises such as abdominal bracing, pelvic tilts, quadruped arm/leg extensions, trunk strengthening prone back extensions and lumbar stretching. |
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 |
|---|---|---|
|
Numeric Pain Rating scale (NPRS) for pain
時間枠:6 weeks
|
The intensity of NSLBP will be measured on the Numeric pain rationg scale which will be assessed verbally by a blinded assessor. This scale is routinely utilized for NSLBP, and is valid, responsive and is easy to administer in a clinical setting. The NPRS is scored on an 11 point scale (0-10) where 0 represents no pain and 10 represents the worst imaginable pain. Excellent interrater reliability, excellent internal consistency for NPRS in participants aged 25-55 (Cronbach's alpha =0.88) |
6 weeks
|
|
Oswestry disability index (ODI)
時間枠:6 weeks
|
The Oswestry Disability Index (ODI) is a validated self-report questionnaire used to measure functional disability related to low back pain. It includes items on pain intensity, personal care, lifting, walking, sitting, standing, sleeping, social life and travel. Scores range from 0-100% where higher scores indicate greater disability. ODI is recognized as a gold standard outcome in NSLBP clinical trails and exhibits excellent reliability and responsiveness in adults with chronic low back pain. |
6 weeks
|
|
Goniometer for Lumbar Range of Motion (ROM)
時間枠:6 weeks
|
Lumbar ROM will be assessed using a manual goniometer according to standard clinical protocols. Common movements measured include lumbar flexion (forward bending), extension (backward bending), lateral flexion (side bending) and rotation. Lumbar ROM assessment has demonstrated acceptable reliability for clinical use and movement deficits have been associated with NSLBP in biomechanical studies. |
6 weeks
|
協力者と研究者
捜査官
- 主任研究者:Mehar Un Nisa Mehar Un Nisa、Riphah International University
研究記録日
主要日程の研究
研究開始 (推定)
一次修了 (推定)
研究の完了 (推定)
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
その他の研究ID番号
- S25C14G30024
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?
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
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