Effects of the Timing of Vagus Nerve Stimulation Combined With Exercise in Chronic Neck Pain
Does Timing Matter? Effects of Transcutaneous Auricular Vagus Nerve Stimulation Before and After Exercise in Chronic Neck Pain: A Randomized Controlled Trial
This randomized controlled trial aims to investigate whether the timing of transcutaneous auricular vagus nerve stimulation (taVNS) relative to exercise influences clinical and autonomic outcomes in individuals with chronic neck pain.
Participants will be randomly allocated to one of three groups: taVNS applied before exercise, taVNS applied after exercise, or exercise alone. All groups will receive a standardized exercise program designed for chronic neck pain. The intervention will be conducted over a 6- to 8-week period.
The effects of the interventions will be evaluated using pain intensity, neck-related disability, sleep quality, heart rate variability, and exercise adherence. The study will determine whether applying taVNS before or after exercise provides additional benefits compared with exercise alone and whether the timing of stimulation influences treatment outcomes.
調査の概要
状態
条件
詳細な説明
Chronic neck pain is a common musculoskeletal condition associated with pain, functional limitations, sleep disturbances, and alterations in autonomic nervous system activity. Exercise therapy is one of the main conservative treatment approaches for chronic neck pain. Transcutaneous auricular vagus nerve stimulation (taVNS) is a non-invasive neuromodulation method that aims to stimulate the auricular branch of the vagus nerve and may influence parasympathetic activity and pain modulation.
The purpose of this randomized controlled trial is to investigate whether the timing of taVNS relative to exercise influences clinical and physiological outcomes in individuals with chronic neck pain.
A total of 81 participants with chronic neck pain will be randomly allocated to three parallel groups. Participants in the first group will receive taVNS before performing a standardized exercise program. Participants in the second group will perform the same exercise program followed by taVNS. Participants in the control group will receive the exercise program alone.
The exercise program will include postural correction exercises, deep cervical flexor activation exercises, cervical mobility exercises, scapular stabilization exercises, and stretching exercises. The intervention period will last approximately 6-8 weeks.
Participants will be evaluated before and after the intervention period. Pain intensity will be assessed using the Numeric Pain Rating Scale, neck-related disability using the Neck Disability Index, sleep quality using the Pittsburgh Sleep Quality Index, and autonomic nervous system activity using heart rate variability, particularly the root mean square of successive differences (RMSSD). Exercise adherence and session attendance will also be recorded.
The study will compare changes in these outcomes among the three groups to determine whether the timing of taVNS relative to exercise influences the effectiveness of rehabilitation in individuals with chronic neck pain.
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：Batuhan YUKSEL, Msc.
- 電話番号：00905334350996
- メール：bthanyksel13@gmail.com
研究場所
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Türkiye
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Kütahya、Türkiye、トルコ（Türkiye）、43100
- Kutahya Health Sciences University Physical Therapy and Rehabilitation Research Center
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副調査官：
- Merve Akdeniz LEBLEBİCİER, MD
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コンタクト：
- Ismail SARACOGLU, PhD
- 電話番号：1499 002742651300
- メール：ismail.saracoglu@ksbu.edu.tr
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主任研究者：
- Batuhan YUKSEL, Msc.
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参加基準
適格基準
就学可能な年齢
- 大人
- 高齢者
健康ボランティアの受け入れ
説明
Inclusion Criteria:
- Diagnosis of chronic neck pain confirmed by a physical medicine and rehabilitation physician.
- Age between 18 and 65 years.
- Neck pain persisting or recurring for at least 3 months.
- Ability to participate in the exercise program included in the study protocol.
- No contraindication to transcutaneous auricular vagus nerve stimulation.
- Willingness to provide written informed consent.
- Willingness to participate regularly in the planned exercise and assessment sessions.
Exclusion Criteria:
- Cervical radiculopathy or specific neurological findings.
- Previous cervical spine surgery.
- Serious cardiovascular disease.
- Serious neurological or systemic disease.
- Pregnancy.
- Orthopedic or musculoskeletal conditions preventing participation in exercise.
- Cognitive or communication problems that prevent completion of the assessment instruments.
- Inability or unwillingness to comply with the study protocol or attend scheduled sessions.
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：taVNS Before Exercise
Participants will receive transcutaneous auricular vagus nerve stimulation before performing the standardized exercise program.
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Transcutaneous auricular vagus nerve stimulation will be delivered non-invasively through an auricular stimulation device targeting the auricular branch of the vagus nerve.
Stimulation will be administered under researcher supervision using standardized stimulation parameters according to the device instructions and study protocol.
Participants will perform a standardized exercise program for chronic neck pain including postural correction, deep cervical flexor activation, cervical mobility, scapular stabilization, and stretching exercises.
Exercises will be performed under researcher supervision during the intervention period.
|
|
実験的：taVNS After Exercise
Participants will first perform the standardized exercise program and will subsequently receive transcutaneous auricular vagus nerve stimulation.
|
Transcutaneous auricular vagus nerve stimulation will be delivered non-invasively through an auricular stimulation device targeting the auricular branch of the vagus nerve.
Stimulation will be administered under researcher supervision using standardized stimulation parameters according to the device instructions and study protocol.
Participants will perform a standardized exercise program for chronic neck pain including postural correction, deep cervical flexor activation, cervical mobility, scapular stabilization, and stretching exercises.
Exercises will be performed under researcher supervision during the intervention period.
|
|
アクティブコンパレータ：Exercise only
Participants will receive the standardized exercise program without transcutaneous auricular vagus nerve stimulation.
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Participants will perform a standardized exercise program for chronic neck pain including postural correction, deep cervical flexor activation, cervical mobility, scapular stabilization, and stretching exercises.
Exercises will be performed under researcher supervision during the intervention period.
|
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 |
|---|---|---|
|
Change in Pain Intensity - Numeric Pain Rating Scale
時間枠：Baseline and immediately after completion of the 6 week interventions
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Pain intensity will be assessed using the Numeric Pain Rating Scale (NPRS).
Participants will rate their neck pain on an 11-point scale ranging from 0 to 10, where 0 indicates "no pain" and 10 indicates "worst imaginable pain."
Higher scores indicate greater pain intensity.
Change from baseline will be compared between groups.
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Baseline and immediately after completion of the 6 week interventions
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Change in Neck-Related Disability - Neck Disability Index
時間枠：Baseline and immediately after completion of the 6 weeks interventions.
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Neck-related disability will be assessed using the Neck Disability Index (NDI).
The questionnaire consists of 10 sections scored from 0 to 5, producing a total score ranging from 0 to 50.
Higher scores indicate greater neck-related disability.
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Baseline and immediately after completion of the 6 weeks interventions.
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Change in Sleep Quality - Pittsburgh Sleep Quality Index
時間枠：Baseline and immediately after completion of the 6 weeks intervention.
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Sleep quality will be assessed using the Pittsburgh Sleep Quality Index (PSQI).
The PSQI evaluates seven components of sleep and provides a global score ranging from 0 to 21.
Higher scores indicate poorer sleep quality.
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Baseline and immediately after completion of the 6 weeks intervention.
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二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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Exercise Adherence
時間枠：Throughout the 6-8-week intervention period.
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Exercise adherence will be assessed based on participant attendance at scheduled treatment sessions.
Adherence will be expressed as the number and/or percentage of completed sessions relative to the total number of planned sessions.
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Throughout the 6-8-week intervention period.
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Change in Heart Rate Variability - RMSSD
時間枠：Baseline and immediately after completion of the 6 weeks intervention.
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Autonomic nervous system activity will be assessed using heart rate variability.
The root mean square of successive differences between normal heartbeats (RMSSD), expressed in milliseconds, will be used as the primary heart rate variability parameter.
Higher RMSSD values generally represent greater parasympathetic/vagal activity.
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Baseline and immediately after completion of the 6 weeks intervention.
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協力者と研究者
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
追加の関連 MeSH 用語
その他の研究ID番号
- BatuPHD
個々の参加者データ (IPD) の計画
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