跳至主要内容
临床试验/NCT06825611
NCT06825611尚未招募不适用

Detecting and Monitoring Scoliosis Without Radiography: Standard Radiographic Monitoring Program Versus Self-Screening with Momentum SpineTM

Children's Hospital Los Angeles0 个研究点目标入组 100 人开始时间: 2025年3月15日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
尚未招募
入组人数
100
主要终点
Accuracy of Scoliosis Progression

研究概览

简要总结

The goal of this clinical trial is for the Momentum SpineTM application to accurately detect scoliosis progression, including accuracy, margin of error, sensitivity, specificity, AUC, and overall agreement with radiographs in 8-18 year olds with adolescent idiopathic scoliosis. The main question it aims to answer [is/are]:

  • Based on previous data it is hypothesize that Momentum SpineTM imaging software will be able to accurately detect scoliosis progression (>= 7 degrees), including accuracy, margin of error, sensitivity, specificity, AUC, and overall agreement with radiographs.
  • Based on the above hypothesis that Momentum SpineTM is able to accurately detect scoliosis and curve progression (>= 7 degrees).
  • It is hypothesized there will be indications for accelerated clinical visits based on at home detection of progression, and that these visits will be accurate and necessary.
  • It is hypothesized that there will be a proportion of standard care visits that are deemed unnecessary, and that the application is able to accurately predict these visits.

Participants will:

  • Use Momentum SpineTM assessment from home to perform body scans at 1-month intervals on personal device and during the clinical visit.
  • Received monthly scans that will be evaluated by the provider using the application.
  • Receive additional scans as warranted.
  • Complete net promoter score (NPS) within the application following completion of a body scan.
  • Complete a patient satisfaction survey following 6 months of application usage.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Supportive Care
盲法
None

入排标准

年龄范围
8 Years 至 18 Years(Child, Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Children between the ages of 8-18 years of age
  • •Confirmed radiographic diagnosis of adolescent idiopathic scoliosis
  • •No history of spinal/ chest surgery.
  • •Participants who have had spine x-rays ±1 week as baseline visit at CHLA will be included in the study.
  • •Participants who have identifiable markings such as tattoos or birthmarks can be included in the study, though their markings will be covered with tape.

排除标准

  • •Participants who have had x-rays in a brace will not be included.
  • •Participants who have had an x-ray from another institution will not be included in the study. X-rays from out of community are typically done with a different and lower quality machine then the one at our institution. Additionally, we do not have consent from outside institutions to use their x-rays for research purposes.
  • •Participants with a confirmed pregnancy will not be included. Pregnancy status will be self-reported by participants.
  • •Participants with the existence of a second deformity which may affect topographic assessment will be excluded (e.g. Limb length discrepancy greater than 2cm).
  • •Families who do not speak English and Spanish will be unable to participate as the application is only available in English and Spanish at this time.
  • •Families who do not have access to their own compatible personal smart phone device will be unable to participate in the study.

研究组 & 干预措施

Momentum Application

Experimental

Patients diagnosed with scoliosis between 8-18 years of age

干预措施: Momentum Application (Device)

结局指标

主要结局

Accuracy of Scoliosis Progression

时间窗: Immediately from enrollment and monthly through study completion

Progression will be defined as a change of greater than or equal to 7 degrees. The progression between the application will be compared to the radiographs done manually, with evaluation of the margin of error, sensitivity, specificity, AUC, and overall agreement with the radiographs.

次要结局

  • Proportion of follow-up visits that were correctly accelerated(Immediately from enrollment through study completion, at an average of 2 years)
  • Necessity of visit(Immediately from enrollment and monthly through study completion)
  • Proportion of avoidable x-rays using Momentum Spine(Immediately from enrollment and monthly through study completion)
  • Patient Satisfaction Survey(Only at the 6 month visit)
  • Net Promoter Score(Immediately from enrollment and monthly through study completion)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Lindsay Andras

Attending Physician

Children's Hospital Los Angeles

相似试验