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

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age8-18
SponsorChildren's Hospital Los Angeles

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

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.

Disqualifiers

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).

Trial design

Design model

Single group

Treatments tested in this trial

  • Momentum Application

    Device

    A mobile application to scan and predict spinal curvature. The application monitors curvature and track changes over time.

Treatment groups

100 Participants
are divided into 1 treatment group
Group A: Momentum ApplicationExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Accuracy of Scoliosis Progression

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.

Time frame
Immediately from enrollment and monthly through study completion

Secondary outcomes

1

Proportion of follow-up visits that were correctly accelerated

Accelerated visits are defined as medical appointments less than 6 months apart (sooner than routine follow-up) suggested by the Momentum Spine mobile application. When Momentum Spine detects progression on 3D models obtained at home, it suggests the clinical team see that patient sooner than the planned semi-annual visit in order to implement treatments earlier (bracing, change in brace, etc.). This endpoint will calculate the percentage of accelerated visits suggested by Momentum Spine where scoliosis progression was present as well as where a change in treatment was required.

Time frame
Immediately from enrollment through study completion, at an average of 2 years
2

Necessity of visit

Coronal curve magnitude between site-specific X-ray measurements and coronal curve magnitude predictions output by Momentum Spine will be compared . The cutoff to determine whether the predicted coronal curve magnitude will be a difference of +/- 7 degrees when compared to the average of the readings from x-rays. Progression noted via Momentum Spine and on radiographs will be compared. Necessary visit = Radiographic Progression \>7 degrees Unnecessary visit = Radiographic Progression \<7 degrees Percentage agreement between Radiographic and MS progression values, with a cutoff point of 7 degrees, will be assessed.

Time frame
Immediately from enrollment and monthly through study completion
3

Proportion of avoidable x-rays using Momentum Spine

An avoidable x-ray is defined as the percentage of radiographs obtained as part of routine semi-annual follow-up that show an absence of scoliosis progression where Momentum Spine was in agreement. This metric demonstrates that Momentum Spine is an accurate tool for determining when spinal radiographs are necessary.

Time frame
Immediately from enrollment and monthly through study completion
4

Patient Satisfaction Survey

The patient satisfaction survey consists of 6 open-ended questions to understand what the experience has been for the individual using the application.

Time frame
Only at the 6 month visit

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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Children's Hospital Los Angeles

Lead sponsor

Momentum Health Inc.

Collaborator

This trial is not recruiting at the moment. You can still explore other options: