Study of Feasibility to Reliably Measure Functional Abilities' Changes in Nonambulant Neuromuscular Patients Without Trial Site Visiting
Assessment of Feasibility and Statistical Reliability of Functional Outcomes Measurement in Neuromuscular Patients Without Trial Site Visiting by Standard Functional Scales and by Special Autonomic Device in Double-blind, Placebo Controlled Study of Cervical Spinal Cord Transdermal Direct Current Stimulation in Patients With Spinal Muscular Atrophy
Clinical trials organization in several neuromuscular disorders (NMD) has some specific issues. Nonambulant status and difficulties with transportation are among them. Moreover a lot of patients with NMD have so poor condition that even short transportation is able to worse it. Such situation forces researchers to limit a region of recruitment for clinical trials and to exclude from trials more severe subgroup of patients, which cause additional issues especially for rare diseases.
The purpose of this study is to prove hypothesis about possibility to reliably monitor patient condition remotely, without trial site visiting. Visit-free study design is potentially able to widen eligible patient population and to decrease patient dropout rate as well as burden of numerous assessments. Meanwhile assessment frequency could be increased enabling monitoring of short fluctuations in patients' condition.
Spinal muscular atrophy (SMA) is a rare neuromuscular condition to which all mentioned above issues are completely applicable. Direct current stimulation (DCS) of neural structures is well studied and safe intervention, however, its effects on SMA patients' strength and durability has not been reported for today. The investigators suppose that investigation of DCS action in SMA patient population is an adequate model for visit-free design feasibility, reliability and sensitivity evaluation.
調査の概要
研究の種類
段階
- 適用できない
連絡先と場所
研究場所
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Kharkiv、ウクライナ、61068
- SI "Institute of Neurology, Psychiatry and Narcology of NAMS of Ukraine"
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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:
- Signed informed consent
- 5q SMA confirmed by molecular testing
Exclusion Criteria:
- Need for ventilation
- Hypersensitivity (pain or allergic reaction) to current stimulation
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:他の
- 割り当て:ランダム化
- 介入モデル:並列代入
- マスキング:4倍
武器と介入
参加者グループ / アーム |
介入・治療 |
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偽コンパレータ:Zero-strength of direct current stimulation
Sham transdermal direct current stimulation of cervical spinal cord
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10 minutes direct current stimulation of 0, 100 microamperes, 1 milliampere strengths applied through dermal electrodes to cervical spinal cord
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実験的:100 microamperes direct current stimulation
Transdermal direct current stimulation of cervical spinal cord
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10 minutes direct current stimulation of 0, 100 microamperes, 1 milliampere strengths applied through dermal electrodes to cervical spinal cord
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実験的:1 milliampere direct current stimulation
Transdermal direct current stimulation of cervical spinal cord
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10 minutes direct current stimulation of 0, 100 microamperes, 1 milliampere strengths applied through dermal electrodes to cervical spinal cord
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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 |
時間枠 |
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Strength Changes from baseline measured by handheld myometry after spinal cord direct current stimulation of different intensity
時間枠:Before and 0, 15, 30 minutes after spinal cord direct current stimulation
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Before and 0, 15, 30 minutes after spinal cord direct current stimulation
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二次結果の測定
結果測定 |
時間枠 |
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Short time fluctuations of Hammersmith Functional Motor Scale indexes
時間枠:Three times, three days consecutive measurement, every two months, assessed up to 6 months
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Three times, three days consecutive measurement, every two months, assessed up to 6 months
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協力者と研究者
捜査官
- 主任研究者:Andriy V. Shatillo, MD, PhD、State Institution "Institute of Neurology, Psychiatry and Narcology of NAMS of Ukraine"
研究記録日
主要日程の研究
研究開始 (実際)
一次修了 (実際)
研究の完了 (実際)
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 (見積もり)
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
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