Effect of Proprioceptive Training on Cervical Sensorimotor Control and Functional Recovery in Patients With Cervical Radiculopathy (Proprioceptive)
Study purpose
The goal of this study is to investigate whether adding cervical proprioceptive training to conventional physiotherapy improves cervical sensorimotor control and functional recovery in patients with chronic cervical radiculopathy.
The study will include 58 participants, aged 35-50 years, with unilateral chronic cervical radiculopathy associated with lower cervical discogenic or spondylotic changes (C5-C6 and/or C6-C7), with symptoms lasting more than three months.
Main research questions
- Does cervical proprioceptive training, in addition to conventional physiotherapy, improve cervical joint position sense (measured by cervical joint position error) compared with conventional physiotherapy alone?
- Does adding cervical proprioceptive training lead to greater improvements in functional disability, pain intensity, functional ability, and cervical range of motion compared with conventional physiotherapy alone?
Comparison groups
Researchers will randomly allocate participants into two groups:
- Experimental group: Participants will receive conventional physiotherapy combined with a structured cervical proprioceptive training programme.
- Control group: Participants will receive conventional physiotherapy alone.
The researchers will compare the two groups to determine whether adding cervical proprioceptive training produces greater improvements in cervical sensorimotor control and functional outcomes.
What participation involves
Participants will be asked to:
- Complete baseline assessments, including the Neck Disability Index (NDI), Visual Analogue Scale (VAS), cervical joint position error (JPE), cervical range of motion (CROM), and Patient-Specific Functional Scale (PSFS).
- Attend their assigned physiotherapy programme three times per week for six weeks, with treatment sessions lasting approximately 60 minutes.
- Follow the treatment programme assigned to their group.
- Complete the same outcome assessments after the six-week intervention period to evaluate changes and compare the results between groups.
調査の概要
状態
状態
条件
条件
介入・治療
介入・治療
詳細な説明
This study is a two-arm, parallel-group randomized clinical trial designed to investigate the effects of a structured cervical proprioceptive training program in individuals with chronic cervical radiculopathy.
Following baseline assessment, participants will be randomly allocated to either an experimental group receiving cervical proprioceptive training or a control group receiving conventional physiotherapy. The intervention period will last six weeks. Treatment sessions will be conducted three times per week, with each session lasting approximately 60 minutes.
The experimental group will receive a supervised cervical proprioceptive training program intended to address impaired cervical sensorimotor control. Training will focus on cervical joint-position awareness, accurate repositioning of the head, and controlled cervical movement. Exercises will be introduced at an appropriate level of difficulty and progressed according to the participant's performance, movement accuracy, tolerance, and ability to complete the tasks with adequate control. Training will be conducted under physiotherapist supervision.
The control group will receive a conventional physiotherapy program over the same six-week treatment period. Treatment will follow the conventional physiotherapy procedures specified in the study protocol and will be delivered according to the standardized intervention plan.
Participants will undergo the planned study assessments before and after the intervention period. The treatment period, session duration, and intervention procedures will be applied consistently according to the study protocol. Attendance and intervention implementation will be monitored throughout the study.
研究の種類
研究の種類
入学 (実際)
入学
段階
段階
- 適用できない
連絡先と場所
研究場所
-
-
Giza Governorate
-
Giza、Giza Governorate、エジプト
- Faculty of physical therapy
-
-
参加基準
適格基準
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:
- Patients of both sexes, diagnosed as having unilateral cervical radiculopathy secondary to discogenic and spondylotic changes at the lower cervical spine (C5-C6 and C6-C7).
- Duration of illness more than "three" months.
- Aged between 35-50 years old.
- Body mass index (BMI) of less than 30 kg/m².
- 4-7/10 score according to VAS (Appendix I).
- Neck Disability Index (NDI) score ≥10/50.
- PSFS scoring of ≥ 5/10
Exclusion Criteria:
- Cervical myelopathy or cervical myelo-radiculopathy.
- Thoracic outlet syndrome.
- Carpal tunnel syndrome.
- Structural spinal instability such as spondylolisthesis.
- Vertebro-basilar artery insufficiency.
- Previous cervicothoracic spine surgery.
- Serious spinal pathology (e.g., tumors or infection).
- Vestibular or severe visual disorders.
- Associated other neurological diseases.
- Recent cervical physiotherapy within the last 2 months
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
アーム数
武器と介入
参加者グループ / アーム参加者グループ / アーム |
介入・治療介入・治療 |
|---|---|
|
アクティブコンパレータ：Control group
Effect of conventional therapy on control group |
Stretching of neck muscles and manual therapy and strengthening exercises |
|
実験的：Study group
Effect of proprioceptive training on stufy group |
Stretching of neck muscles and manual therapy and strengthening exercises Proprioceptive training using head mounted laser and target grids and tracking grids |
この研究は何を測定していますか？
主要な結果の測定
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Joint position error
時間枠：6 weeks
|
Deviation from normal joint position is calculated |
6 weeks
|
|
Patient specific functional scale
時間枠：6 weeks
|
Measures function of cervical radiculopathy patient |
6 weeks
|
協力者と研究者
研究記録日
主要日程の研究
研究開始 (実際)
研究開始
一次修了 (実際)
一次修了
研究の完了 (実際)
研究の完了
試験登録日
最初に提出
最初に提出
QC基準を満たした最初の提出物
QC基準を満たした最初の提出物
最初の投稿 (実際)
最初の投稿
学習記録の更新
投稿された最後の更新 (実際)
投稿された最後の更新
QC基準を満たした最後の更新が送信されました
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
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
その他の研究ID番号
- P.T.REC/012/006393
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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