试验雷达 AI | ||
|---|---|---|
临床试验 NCT05901259 (EXOREG) 针对脑瘫,多发性硬化症,中风,神经系统疾病,纤维肌痛目前招募中。请查看临床试验雷达卡片视图和 AI 发现工具了解所有详情,或在此提出任何问题。 | ||
一个试验符合筛选条件
卡片视图
The EXOPULSE Study - a Database for Routine Follow-up of Clinical Outcomes (EXOREG) 200 儿科
临床试验详情主要以英语提供。然而,试验雷达 AI可以提供帮助!只需点击“试验详解”即可查看和讨论您选择的语言的试验信息。
临床试验NCT05901259 (EXOREG)是一项针对脑瘫,多发性硬化症,中风,神经系统疾病,纤维肌痛的观察研究试验,目前试验状态为招募中。试验始于2026年2月18日,计划招募200名患者。该研究由Exoneural Network AB主导,预计于2027年12月31日完成。试验数据来源于ClinicalTrials.gov,最后更新时间为2026年2月27日。
简要概括
The objective is to explore the potential short and long-term impact of the EXOPULSE Mollii Suit and EXOPULSE Suit on subjects with CP, MS, stroke, fibromyalgia or other neurologic disorders which may cause such types of symptoms, and to identify high responders among the sub-categories of the diagnoses. The primary endpoint will be improvements in the Berg/Pediatric Balance Scale (BBS/PBS) as a measurement of balanc...显示更多
详细描述
The observational study (also referred to as the 'registry') is designed to demonstrate the impact of EXOPULSE Mollii Suit and EXOPULSE Suit on relaxation of muscles, muscle activation, local blood circulation and chronic pain relief.
The subjects will serve as their own control and the data will be collected before, during and after the treatment period. As the electrical stimulation from the suit usually is above ...
显示更多官方标题
The EXOPULSE Study - a Database for Routine Follow-up of Clinical Outcomes
疾病
脑瘫多发性硬化症中风神经系统疾病纤维肌痛其他研究标识符
- EXOREG
- CIV-22-08-040366
试验组/干预措施
| 参与者组/试验组 | 干预措施/治疗方法 |
|---|---|
不适用 | EXOPULSE Mollii Suit and EXOPULSE Suit The registry is designed to demonstrate the impact of EXOPULSE Mollii Suit or EXOPULSE Suit on muscle relaxation, muscle activation, local blood circulation and/or chronic pain relief. The subjects included use the suit for 60 minutes every other day, unless other is specified by the Investigator, in their home environment for up to a maximum of 2 consecutive weeks. Qualitative and quantitative measures will be colle...显示更多 |
主要终点
次要终点
| 结果指标 | 度量标准描述 | 时间框架 |
|---|---|---|
Berg's Balance Scale | Change in balance will be assessed using the 14-item Berg Balance Scale (BBS) which has good psychometric properties in Patients with Multiple Sclerosis (concurrent validity, interrater reliability). The scale rates the balance using 56 points, with higher scores indicating better balance abilities. A score equal to or below 45 is commonly associated with risk of fall across the literature. | To be assessed at baseline, after 60 minutes stimulation (T1), and after 2 weeks of home use (T2). |
| 结果指标 | 度量标准描述 | 时间框架 |
|---|---|---|
Timed Up and Go (TUG), if applicable for the patient | Change in walking velocity will be assessed with TUG. Patients have to stand up from a chair when they hear the verbal instruction "go", walk a distance of 3 meters, turn around, walk back to the chair and sit down. Timing starts with the verbal instruction "go' and stops when the patients return to the seated position. The score consists of the time taken to complete the test activity, measured in seconds. | To be assessed at baseline, immediately after 60 minutes stimulation (T1), and after two weeks of home use (T2). |
10 m Walk Test, if applicable for the patient | The 10mWT is used to assess the change in walking speed in meters/second (m/s) over a short distance. | To be assessed at baseline, immediately after 60 minutes stimulation (T1), and after two weeks of home use (T2). |
Numeric Rating Scale (NRS), if applicable for the patient | The change in pain will be assess with NRS. NRS measures the subjective intensity of pain, where 0=no pain and 10=worst pain imaginable. | To be assessed at baseline, immediately after 60 minutes stimulation (T1), after two weeks of home use (T2) and during the two additional phone calls (T1,5 and T3 respectively). |
EQ-5D-5L, if applicable for the patient | The change in quality of life will be assessed with EQ-5D, which is an instrument that evaluates the generic quality of life. Designed as a self-completion questionnaire, it embodies two components, a health state description followed by an evaluation.The respondent classifies his or her prevailing state of health by selecting one of three different levels of problem severity within each of five health domains. | To be assessed at baseline, after two weeks of home use (T2) and during the two additional phone calls (T1,5 and T3 respectively). |
Revised Fibromyalgia Impact Questionnaire (FIQR), if applicable for the patient | The FIQR evaluates the function, overall impact and symptoms of fibromyalgia over the last 7 days.
The Fibromyalgia Impact Questionnaire (FIQ) is a well-established and commonly used instrument to evaluate Fibromyalgia patients. The FIQR is a revised version of the FIQ, that has the same 3 domains, i.e. function, overall impact and symptoms. The FIQR also consists of modified function questions as well as questions on memory, tenderness, balance and environmental sensitivity. All questions are graded on a 0-10 numeric scale. | To be assessed at baseline, after 2 weeks of home use and during the two additional phone calls (T1,5 and T3 respectively). |
Box and Block Test (BBT), if applicable to the patient | The Box and Block Test (BBT) measures unilateral gross manual dexterity in patients with neurological diagnoses. Patients are scored based on the number of blocks transferred from one compartment to the other compartment in 60 seconds | To be assessed at baseline, immediately after 60 minutes stimulation (T1) and after two weeks of home use (T2) |
12-item Multiple Sclerosis Walking Scale (MSWS-12) , if applicable for the patient | The MSWS-12 is a self-report measure of the impact of MS on the individual's walking ability. It contains 12 questions with Likert-type responses and has a recall period of 2 weeks. The psychometric properties of the MSWS-12 have been extensively evaluated in diverse MS populations in both community and hospital settings, with demonstration of internal consistency, high reliability and validity, and good generalizability. The MSWS-12 is less prone to floor and ceiling effects than are other tools, suggesting adequate assessment of the impact of walking impairment across the range of disability. | To be assessed at baseline, after two weeks of home use (T2) and during the two additional phone calls (T1,5 and T3 respectively). |
Widespread Pain Index (WPI) , if applicable for the patient | The WPI is based on a standardized questionnaire. Patients are asked in which regions of the body they have experienced pain in the past seven days. In total, the WPI measures pain in 19 defined body regions or pain zones. It is supposed to be used in combination with the Symptom Severity Scale. | To be assessed at baseline, immediately after 60 minutes stimulation (T1), after two weeks of home use (T2) and and during the two additional phone calls (T1,5 and T3 respectively). |
Symptom Severity Scale (SSS) , if applicable for the patient | SSS calculates severity scores of a number of Fibromyalgia-related symptoms. Together, the WPI and SSS can be used as diagnostic criteria for Fibromyalgia. | To be assessed at baseline, after two weeks of home use (T2) and during the two additional phone calls (T1,5 and T3 respectively). |
参与助手
资格标准
适龄参与研究
儿童, 成人, 老年人
最低年龄要求
2 Years
适龄性别
全部
- Diagnosed with CP, MS, stroke, fibromyalgia or other neurologic disorder that may cause such type of symptoms.
- Diagnosed >6 months prior to inclusion in case of MS or stroke as well as >1 month prior to inclusion in the case of fibromyalgia.
- Give written informed consent
- Cognitively able to understand and follow verbal and/or written instructions
- A minimum age of 2 years
- Any of the contraindications listed in the instructions for use of the EXOPULSE Mollii Suit or EXOPULSE Suit
- Being introduced to any new medication affecting the neuromuscular activity during the study period
- Using botulinum toxin <3 month before or during the study period
- Subjects <100 cm and <13 kg
- Subjects >205 cm and >115 kg
研究中心联系人
联系人: Milana Mileusnic, PhD, +43 6648415079, [email protected]
联系人: Sanna Dünesius, MSc, +46 706243064, [email protected]
1 位于 1 个国家/地区的研究中心
Stockholm County
Ottobock Care Sverige, Bergshamra, Stockholm County, 170 73, Sweden
Ines Cunha, 联系人, [email protected]
招募中