Noninvasive Brain Stimulation for Cervical Dystonia (NetworkStim)
The Effect of Noninvasive Brain Stimulation on Symptoms of Cervical Dystonia
The primary aim of this study is to assess whether continuous theta-burst stimulation (cTBS) can be helpful in reducing symptoms of idiopathic cervical dystonia. This will be a parallel-group, randomised, sham-controlled, double blind clinical trial. Patients and investigators measuring patient symptoms clinical scales will be blinded from allocation group, investigators delivering the intervention will not be blinded, as this is not feasible. Real cTBS will be compared to sham cTBS, with patients allocated to these two groups with a 1:1 recruitment ratio.
Bilateral cTBS will be delivered four times daily, over eight days, for a total of 32 bilateral cTBS sessions. The primary outcome is the Toronto Western Spasmodic Torticollis Rating Scale (TWSTRS). This will be administered at T1 (pre-cTBS), T2 (day 10, following days 2-9 where patients received the intervention), T3 (2 weeks post the final session of cTBS), and T4 (4-5 weeks post the final session of cTBS).
Secondary outcomes will be the TWSTRS subscales (severity, disability, pain), Quality of Life scale, Global dystonia severity rating scale (GDS), Fahn Tolosa Marin (FTM) modified (to include only questions relevant to head/neck tremor) tremor scale, kinematic data of patient's movement patterns, motor evoked potentials (MEPs), and resting-state fMRI data (fMRI).
調査の概要
状態
条件
詳細な説明
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:Daniel T Corp, PhD
- 電話番号:+393445660971
- メール:danieltcorp@gmail.com
研究連絡先のバックアップ
- 名前:Ambra Salvati
- 電話番号:+393491028595
- メール:ambra.salvati@unicampus.it
研究場所
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Roma
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Roma、Roma、イタリア、00128
- Università Campus Bio-Medico
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コンタクト:
- Vincenzo Di Lazzaro, MD
- 電話番号:+39 06225411220
- メール:v.dilazzaro@policlinicocampus.it
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コンタクト:
- Ambra Salvati, Psy.D.
- 電話番号:+39 3491028595
- メール:ambra.salvati@unicampus.it
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副調査官:
- Daniel T Corp, PhD
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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
- Aged between 18 and 85 years
- Diagnosis of idiopathic cervical dystonia made by an expert physician
- Last botulinum toxin injection administered at least two months before the start of participation in the study (Albanese, Abbruzzese et al. 2015)
Exclusion Criteria
- Head or neck trauma occurring less than 12 months before the onset of dystonia
- Acquired dystonia (e.g., drug-induced, brain lesions or trauma)
- History of major psychiatric disorders (e.g., bipolar disorder, schizophrenia, obsessive-compulsive disorder)
- History of neurological diseases other than CD (e.g., epilepsy, Parkinson's disease)
- Other contraindications for TMS or brain MRI (e.g., metal in the head)
- Pregnant or breastfeeding women
- History of substance abuse or dependence
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 |
|---|---|
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実験的:Active cTBS
The patients of this group will receive 4 sessions of bilateral somatosensory cortex cTBS per day for 8 days
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Continuous theta-burst stimulation (cTBS) will be delivered using a Magstim Rapid machine connected to a 70mm cooled coil at 80% of a participants resting motor threshold (RMT).
cTBS will consist of three-pulse bursts at 50Hz repeated every 200ms (5Hz) for 40 seconds (600 pulses total) (Huang, Edwards et al. 2005).
All cTBS procedures will be conducted bilaterally, with application first over the left hemisphere, before moving to the right (approximately one minute will separate each hemisphere).
Bilateral cTBS will be delivered four times daily, over eight days, for a total of 32 bilateral cTBS sessions.
This 4x day protocol will follow prior studies in neglect patients, delivered at time intervals of 0, 15, 60, and 75 minutes (Nyffeler, Cazzoli et al. 2008, Cazzoli, Müri et al. 2012, Nyffeler, Vanbellingen et al. 2019).
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偽コンパレータ:Sham cTBS
The patients of this group will receive 4 sessions of bilateral somatosensory cortex cTBS per day for 8 days, delivered using a sham TMS coil.
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Sham cTBS procedures will be identical to those in the active cTBS arm but applied using a 70mm sham TMS coil.
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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 |
|---|---|---|
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Symptoms of cervical dystonia - TWSTRS total score
時間枠:For a single patient, a minimum of 6 weeks and a maximum of 16 weeks
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The total score on the Toronto Western Spasmodic Torticollis Rating Scale
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For a single patient, a minimum of 6 weeks and a maximum of 16 weeks
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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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Symptoms of cervical dystonia - TWSTRS subscales
時間枠:For a single patient, a minimum of 6 weeks and a maximum of 16 weeks
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The scores on each of the subscales of the Toronto Western Spasmodic Torticollis Rating Scale (severity, disability, pain)
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For a single patient, a minimum of 6 weeks and a maximum of 16 weeks
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Symptoms of cervical dystonia - kinematic recordings
時間枠:For a single patient, 10 days. Pre and post cTBS
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Metrics of patients' head and neck movements from a wearable motion sensor
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For a single patient, 10 days. Pre and post cTBS
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Motor evoked potentials
時間枠:For a single patient, 10 days. Pre and post cTBS
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Motor evoked potential amplitudes from input-output curves, measured using surface electromyography
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For a single patient, 10 days. Pre and post cTBS
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Magnetic resonance imaging
時間枠:For a single patient, 10 days. Pre and post cTBS
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Functional connectivity changes from pre-defined regions of interest in the brain
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For a single patient, 10 days. Pre and post cTBS
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Fahn Tolosa Marin tremor scale
時間枠:For a single patient, a minimum of 6 weeks and a maximum of 16 weeks
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Measurement of head and neck tremor
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For a single patient, a minimum of 6 weeks and a maximum of 16 weeks
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Global dystonia severity rating scale
時間枠:For a single patient, a minimum of 6 weeks and a maximum of 16 weeks
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Measurement of dystonia in other body parts
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For a single patient, a minimum of 6 weeks and a maximum of 16 weeks
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協力者と研究者
捜査官
- 主任研究者:Vincenzo Di Lazzaro, MD、Campus Bio-Medico Hospital
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
キーワード
その他の研究ID番号
- NetworkStim 270.25 CET2 cbm
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?
IPD プランの説明
IPD 共有時間枠
IPD 共有アクセス基準
IPD 共有サポート情報タイプ
- STUDY_PROTOCOL
- SAP
- ICF
- ANALYTIC_CODE
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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