Sensorimotor Training With a Mobilized Balance Platform in Patients With Chronic Low Back Pain
2026年5月16日 更新者：Sefa Gümrük Aslan、Gaziler Physical Medicine and Rehabilitation Education and Research Hospital
Effects of a Sensorimotor Training Protocol Using a Mobilized Balance Platform on Proprioceptive System, Movement Control, and Quality of Life in Patients With Chronic Low Back Pain
This randomized controlled study aims to investigate the effects of a sensorimotor training protocol using a mobilized balance platform device on proprioceptive system function, movement control, balance, physical performance, pain severity, and quality of life in patients with chronic low back pain. A total of 44 patients with chronic low back pain will be recruited from the outpatient clinic of Gaziler Physical Medicine and Rehabilitation Training and Research Hospital.
Participants will be randomly assigned to either a sensorimotor training group or a control group. The intervention group will receive sensorimotor training using the Huber 360 balance system, while the control group will perform a home exercise program including stretching, spinal mobility, lumbopelvic control, and balance exercises.
Pain severity, proprioception, functional status, balance, physical performance, and quality of life will be assessed before and after treatment by an assessor blinded to group allocation.
調査の概要
研究の種類
介入
入学 (推定)
44
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：Sefa Gumruk Aslan
- 電話番号：+903122911503
- メール：sefagumrukk@gmail.com
研究場所
-
-
-
Ankara、トルコ（Türkiye）
- 募集
- Ankara Gaziler physical therapy and rehabilitation hospital
-
コンタクト：
- Sefa Gumruk Aslan
- 電話番号：+903122911503
- メール：sefagumrukk@gmail.com
-
-
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:
- Individuals aged between 18 and 55 years
- Presence of chronic low back pain lasting at least 3 months
- Pain intensity score of 3 or higher on the Visual Analog Scale (VAS)
- Individuals with sufficient cognitive ability to understand and follow study procedures
- Willingness to participate voluntarily in the study
Exclusion Criteria:
- Participation in a similar training program within the last 12 months
- History of lower extremity or spinal surgery
- Presence of non-mechanical low back pain, inflammatory disease, or tumor
- Uncontrolled hypertension or cardiac disease
- History of malignancy
- Presence of radicular symptoms associated with low back pain
- Progressive neurological deficits
- Neurogenic claudication
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：独身
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
|
アクティブコンパレータ：Home Exercise Program
Participants in this group will perform a home exercise program including warm-up and stretching exercises, spinal mobility exercises, lumbopelvic control exercises, and balance exercises.
The program will be performed for 30 minutes per session, twice weekly for 5 weeks.
|
Participants will perform a home exercise program including warm-up and stretching exercises, spinal mobility exercises, lumbopelvic control exercises, and balance exercises.
The program will be performed for 30 minutes per session, twice weekly for 5 weeks.
|
|
実験的：Huber 360 Sensorimotor Training
Participants in this group will receive a sensorimotor training protocol using the Huber 360 balance system.
The intervention will include progressive rotational and oscillatory exercises aimed at improving proprioception, balance, neuromuscular control, and movement control.
Sessions will be performed for 30 minutes, twice weekly for 5 weeks.
|
Participants will perform a home exercise program including warm-up and stretching exercises, spinal mobility exercises, lumbopelvic control exercises, and balance exercises.
The program will be performed for 30 minutes per session, twice weekly for 5 weeks.
Participants will receive sensorimotor training using the Huber 360 balance system.
The protocol will include progressive rotational and oscillatory exercises designed to improve proprioception, balance, neuromuscular control, and movement control in patients with chronic low back pain.
Sessions will be performed for 30 minutes, twice weekly for 5 weeks.
|
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 |
|---|---|---|
|
Lumbar Proprioception Assessment
時間枠：Before treatment and immediately after completion of the 5-week intervention program
|
Lumbar proprioception will be assessed using lumbar repositioning tests at 60 degrees flexion and 15 degrees extension.
Participants will be asked to reproduce target lumbar positions, and the angular repositioning error will be recorded.
Lower repositioning error values indicate better lumbar proprioceptive accuracy.
|
Before treatment and immediately after completion of the 5-week intervention program
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Pain Severity Assessed by Visual Analog Scale
時間枠：Before treatment and immediately after completion of the 5-week intervention program
|
Pain intensity will be assessed using a 10-cm Visual Analog Scale (VAS).
Scores range from 0 to 10, where 0 indicates no pain and 10 indicates the worst imaginable pain.
Higher scores indicate greater pain severity.
|
Before treatment and immediately after completion of the 5-week intervention program
|
|
Functional Status Assessed by Oswestry Disability Index
時間枠：Before treatment and immediately after completion of the 5-week intervention program
|
Functional disability related to low back pain will be assessed using the Oswestry Disability Index (ODI).
Higher scores indicate greater disability.
|
Before treatment and immediately after completion of the 5-week intervention program
|
|
Balance and Limits of Stability Assessed by Huber 360
時間枠：Before treatment and immediately after completion of the 5-week intervention program
|
Static balance, dynamic balance, and limits of stability will be assessed using the Huber 360 balance system.
Better balance performance and improved stability limits indicate better postural control.
|
Before treatment and immediately after completion of the 5-week intervention program
|
|
Lumbar Flexion Range of Motion
時間枠：Before treatment and immediately after completion of the 5-week intervention program
|
Physical performance will be assessed using a Physical Performance Test Battery including lumbar flexion range of motion, 50-step walking test, 5-minute walking test, five-repetition sit-to-stand test, ten-repetition trunk flexion test, and forward reaching with weight.
|
Before treatment and immediately after completion of the 5-week intervention program
|
|
Quality of Life Assessed by Short Form-36
時間枠：Before treatment and immediately after completion of the 5-week intervention program
|
Quality of life will be assessed using the Short Form-36 (SF-36).
Higher scores indicate better health-related quality of life.
|
Before treatment and immediately after completion of the 5-week intervention program
|
|
50-Step Walking Test
時間枠：Before treatment and immediately after completion of the 5-week intervention program
|
he time required to complete the 50-step walking test will be recorded in seconds
|
Before treatment and immediately after completion of the 5-week intervention program
|
|
Five-Minute Walking Test
時間枠：Before treatment and immediately after completion of the 5-week intervention program
|
The time required to complete five sit-to-stand repetitions will be recorded in seconds.
|
Before treatment and immediately after completion of the 5-week intervention program
|
|
Ten-Repetition Trunk Flexion Test
時間枠：Before treatment and immediately after completion of the 5-week intervention program
|
The time required to complete ten trunk flexion repetitions will be recorded in seconds.
|
Before treatment and immediately after completion of the 5-week intervention program
|
|
Forward Reaching with Weight Test
時間枠：Before treatment and immediately after completion of the 5-week intervention program
|
Forward reaching distance while holding weight will be measured in centimeters.
|
Before treatment and immediately after completion of the 5-week intervention program
|
協力者と研究者
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。
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 (実際)
2026年5月4日
一次修了 (推定)
2026年10月30日
研究の完了 (推定)
2026年11月30日
試験登録日
最初に提出
2026年5月3日
QC基準を満たした最初の提出物
2026年5月16日
最初の投稿 (実際)
2026年5月22日
学習記録の更新
投稿された最後の更新 (実際)
2026年5月22日
QC基準を満たした最後の更新が送信されました
2026年5月16日
最終確認日
2026年5月1日
詳しくは
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。