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临床试验 NCT06962618 (THRIVE-CP) 针对脑瘫目前尚未招募。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。 | ||
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Home-Based Training With Feedback to Improve Outcomes in Adolescents and Young Adults With Cerebral Palsy.. (THRIVE-CP) 70 居家 真实世界证据 青少年 短期
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临床试验NCT06962618 (THRIVE-CP)是一项针对脑瘫的干预性研究试验,当前状态为尚未招募。试验尚未开始,计划于2025年12月1日开始,预计招募70名患者。该研究由哥本哈根大学主导,计划于2029年2月1日完成。试验数据来源于ClinicalTrials.gov,最后更新时间为2025年5月8日。
简要概括
This clinical trial aims to determine whether extrinsic feedback through music enhances the effects of home-based motor training for adolescents and young adults with cerebral palsy (CP) and whether feedback improves adherence to the training program.
The main questions it aims to answer are:
- Does extrinsic feedback improve real-world movement more than home training alone?
- Do participants receiving extrinsic f...
官方标题
The THRIVE-CP Trial - Targeted Home-Based Training With Real-Time Feedback to Improve Versatile Movement Behaviors and Enhance Outcomes in Adolescents and Young Adults With Cerebral Palsy: Protocol for a Randomized Controlled Trial.
疾病
脑瘫其他研究标识符
- THRIVE-CP
NCT编号
实际开始日期
2025-12-01
最近更新发布
2025-05-08
预计完成日期
2029-02-01
计划入组人数
70
研究类型
干预性研究
试验分期 (阶段)
不适用
试验状态
尚未招募
关键词
cerebral palsy
Home-based training
Extrinsic feedback
Movement behavior
Motor learning
Home-based training
Extrinsic feedback
Movement behavior
Motor learning
主要目的
治疗方法
分配方式
随机
干预模型
平行
盲法
四盲
试验组/干预措施
| 参与者组/试验组 | 干预措施/治疗方法 |
|---|---|
实验性Music Motion Group | Music Motion Group Participants will engage in personalized, home-based motor training programs tailored to their individual goals. Each will wear a wireless Inertial Measurement Unit (IMU) on the targeted body part, which transmits movement data via Bluetooth to a tablet app. The training emphasizes task specificity and intensity, with five virtual check-ins to review progress and adjust training parameters.
The intervention studied ...显示更多 |
阳性对照Control | 对照 Participants will follow personalized, home-based motor training programs designed like the Music motion group. They will wear a wireless Inertial Measurement Unit (IMU) on the targeted body part, transmitting movement data via Bluetooth to a tablet app. However, unlike the Music Motion Feedback group, participants in the Control group will not receive any extrinsic feedback during their training. |
主要终点
次要终点
| 结果指标 | 度量标准描述 | 时间框架 |
|---|---|---|
Percentage change in daytime movement of the trained extremity (right or left arm or leg) as measured by 3-axis accelerometer and gyroscope data analyzed via deep-learning neural network | Movement data will be collected using seven Inertial Measurement Units (IMUs) worn continuously for 72 hours at three time points: baseline, 12 weeks (end of intervention), and 24 weeks (follow-up).
IMUs will be attached to the sternum, wrists, thighs, and lower legs using adhesive patches and will capture 3-axis accelerometer and gyroscope data. A validated custom neural network (Novosel et al. 2023) will convert signals into images and analyze them using convolutional layers to extract features related to movement behaviors. The primary metric will be the percentage change (minutes a day) in real-world daytime movement of the trained limb, computed relative to baseline.
This outcome reflects changes in functional mobility resulting from the motor training intervention. | Baseline, at 12 weeks (end of intervention period), and at 24 weeks (long term follow up) |
| 结果指标 | 度量标准描述 | 时间框架 |
|---|---|---|
Number of daily logins to the tablet app | Attendance will be measured as the number of times participants log into the tablet app during the intervention.
Unit of Measure: Number of logins | The app stores the data during the intervention period and will be collected at 12 weeks (end of intervention period) |
Daily session duration recorded in the tablet app | Adherence will be assessed by the average length of each daily training session. This outcome reflects how long participants remain engaged with the motor training program once they log in.
Unit of Measure: Minutes | The app stores the data during the intervention period and will be collectedThe app stores the data during the intervention period and will be collected at 12 weeks (end of intervention period) |
Time spent moving the targeted extremity during training recorded in the tablet app | This measure reflects adherence by quantifying the active movement time of the trained extremity during each training session.
Unit of Measure: Minutes | The app stores the data during the intervention period and will be collected The app stores the data during the intervention period and will be collected at 12 weeks (end of intervention period) |
Time spent within target movement intensity threshold recorded in the tablet app | For participants in the Music Motion Feedback group, adherence will also be evaluated by measuring the time spent at or above a predefined movement intensity threshold.
Unit of Measure: Minutes | The app stores the data during the intervention period and will be collected The app stores the data during the intervention period and will be collected at 12 weeks (end of intervention period) |
Action Research Arm Test (ARAT) total score - (Upper Extremity) | In participants engaged in upper extremity training, the ARAT will be used to evaluate upper extremity functional capacity. It consists of 19 items assessing grasp, grip, pinch, and gross movement. Scores range from 0 to 57, with higher scores indicating better arm function.
Time Frame: Baseline, 12 weeks (end of intervention), and 24 weeks (follow-up) Unit of Measure: ARAT total score (0-57) | Baseline, at 12 weeks (end of intervention period), and at 24 weeks (long term follow up) |
Maximum isometric arm strength - (Upper Extremity) | Participants engaged in upper extremity training will have the isometric strength of the targeted upper extremity measured using a handheld dynamometer. They will perform maximum voluntary contractions against resistance, and the peak force will be recorded.
Unit of Measure: Kilograms of force (kgf) | Baseline, at 12 weeks (end of intervention period), and at 24 weeks (long term follow up) |
Maximum grip strength - (Upper Extremity) | Participants who are engaged in upper extremity training will have their grip strength of the targeted upper limb measured using a hand dynamometer. The highest of three attempts will be recorded.
Unit of Measure: Kilograms of force (kgf) | Baseline, at 12 weeks (end of intervention period), and at 24 weeks (long term follow up) |
Gross Motor Function Measure-66 (GMFM-66) total score - (Lower Extremity) | In participants who are engaged in lower extremity training the GMFM-66 will be used to assess gross motor function. It evaluates activities such as standing, walking, and running. Scores range from 0 to 100, with higher scores indicating better function.
Unit of Measure: GMFM-66 total score (0-100) | Baseline, at 12 weeks (end of intervention period), and at 24 weeks (long term follow up) |
Maximum isometric leg strength - (Lower Extremity) | The isometric strength of the trained leg will be assessed using a handheld dynamometer. Participants will perform maximum voluntary contractions, and peak force will be recorded.
Unit of Measure: Kilograms of force (kgf) | Baseline, at 12 weeks (end of intervention period), and at 24 weeks (long term follow up) |
Distance walked during the Six-Minute Walk Test (6MWT) - (Lower Extremity) | The 6MWT will be used to evaluate walking endurance and aerobic capacity. Participants engaged in lower extremity training will walk as far as possible in six minutes along a flat, indoor course.
Time Frame: Baseline, 12 weeks, and 24 weeks Unit of Measure: Meters walked | Baseline, at 12 weeks (end of intervention period), and at 24 weeks (long term follow up) |
参与助手
资格标准
适龄参与研究
儿童, 成人
最低年龄要求
15 Years
适龄性别
全部
- Clinical diagnosis of cerebral palsy
- Sensorimotor deficits in at least one limb
- Demonstrated motivation to develop or regain motor skills, indicated by the expression of specific goals
- Ability to follow instructions independently or with caregiver support
- Ability to provide informed consent
- Diagnosis of dyskinetic cerebral palsy
- Presence of significant health risks that could interfere with participation
- Surgery or first Botox injection within one month before the trial or during the trial period
研究责任方
Ivana Bardino Novosel, 主要研究者, Principal Investigator, University of Copenhagen
研究中心联系人
联系人: Ivana B Novosel, PhD student, 27328961, [email protected]
联系人: Jakob Lorentzen, Professor, +4531521131, [email protected]
1 位于 1 个国家/地区的研究中心
CP Youth Clinic, Copenhagen University Hospital - Rigshospitalet, Copenhagen, Denmark
Jakob Lorentzen, Professor, 联系人, [email protected]