Scoliosis Idiopathic Adolescent Treatment3DSCOLIBRACENCT06785207
Rethinking Rigidity: Development of a 3D-Printed Scoliosis Brace With Varying Flexibility
A study testing 3D-printed scoliosis brace in people with Scoliosis Idiopathic Adolescent Treatment, run by Baylor College of Medicine at 2 sites in United States.
Trial summary
Scoliosis bracing is an effective treatment method for idiopathic scoliosis, but only if worn consistently for many hours a day. Unsurprisingly, brace discomfort is a significant deterrent against treatment adherence. Read more about this study
- Who is it for?
- Ages 8 to 18 years
- Conditions the study is for
- Scoliosis Idiopathic Adolescent Treatment
- What is being tested?
- 3D-printed scoliosis brace
- Type of treatment
- Medical device
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 5 participants
- Where
- 2 sitesUnited States
- Study dates
- 1 Apr 2025to 31 Oct 2026
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 8 to 18 years
- All sexes
- No healthy volunteers
- Child, Adult
Who may be able to join
- Have a diagnosis of juvenile idiopathic scoliosis or adolescent idiopathic scoliosis
- Have a Cobb angle between 20-40 degrees
- Are between ages 8-18
- Present as Risser 2+ on x-ray
- Currently wear a traditionally fabricated scoliosis brace
- Have good brace adherence in current brace (self-reported to be 75% of prescribed time)
Show all 9Show fewer
- Be an established patient of Align Clinic and Dr. Timothy Borden
- Speak English (survey and semi-structured interview will only be available in English)
- Assent and receive parental consent
Who cannot join
- Have a diagnosis other than juvenile idiopathic scoliosis or adolescent idiopathic scoliosis
- Have a Cobb angle outside the range of 20-40 degrees
- Present as Risser 0 or 1
- Do not currently wear a traditionally fabricated scoliosis brace
- Have poor adherence in their current brace
- Do not speak English
- Are not willing participate in the study
Trial locations and contacts
2 sites in 1 country. Contact the study team or a site near you to ask about taking part.
United States2 sites, 1 recruiting
- Completed
University of Texas Health Science Center at Houston
Houston, Texas, 77030
- Recruiting
Align Clinic
The Woodlands, Texas, 77380
Megan EG Castille, MS, 713-798-3098, megan.glahn@bcm.edu
About this study
Scoliosis bracing is an effective treatment method for idiopathic scoliosis, but only if worn consistently for many hours a day. Unsurprisingly, brace discomfort is a significant deterrent against treatment adherence. For decades, custom braces for idiopathic scoliosis have been fabricated using one of three materials - copolymer, polypropylene, or polyethylene. The application of the biomechanical principles behind bracing have improved over the years, but the materials have not. The investigators' goal is to expand fabrication options by testing a 3D-printed scoliosis brace with variable flexibility. The aim is to improve patients' perceived brace comfort.
After optimizing the brace design, the investigators will collect patient feedback about the design from currently braced participants. These participants understand what a standard brace feels like and will provide impactful feedback.
Read the detailed description
After optimizing the brace design, the investigators will collect patient feedback about the design from currently braced participants. Once a participant enrolls in the study, the 3D printed brace will be made using the exact same shape as their current brace. The standard fabrication process includes the following:
- Certified orthotist completes a full evaluation
- Taking a scan of the patient's body
- Modifying, or editing, the patient's body shape using Computer-Aided-Design and applying corrective pressures against the apex of the scoliotic curve
- Carving a positive foam model of the modified shape and thermoforming the polypropylene plastic over the positive foam model
These steps were already completed to make the participant's current brace, which has been deemed acceptable by their medical team, including the PI and Dr. Timothy Borden. To reduce the number of variables present, the 3D printed brace will be made using the exact same shape as their current brace. The only difference is the fabrication technique (step 4). Instead of carving a foam mode and thermoforming, the exact brace shape will be directly 3D printed. Therefore, no additional x-rays, scans, or measurements are required from the participants. The standard fabrication process and research activities are outlined in attachment titled "Fabrication Process Outline."
Once the 3D printed brace has been fabricated, the participant will come in to be fit with the brace. A standard fitting involves trimming the brace, adding straps, heating and flaring to improve comfort, and potentially adding padding. The PI is a scoliosis bracing specialist and will be the lead orthotist during the fitting process to ensure that best practices are followed.
Following the fitting, the participant will provide test out the 3D printed brace for comfort by performing a series of tasks. The activities will include the following: sitting in a chair, picking an item up from the floor while standing, picking an item up from the floor while sitting, stepping onto a stool, jogging in place for 10s, performing the hula hoop Wii-fit game, lying down on an exam table, and donning shoes. All data collection will take place via the survey platform Qualtrics.
If the participants feel comfortable in the brace and pass a skin check, the participants will then take the brace home and wear it for 1 week. They will return for the 1-week follow-up appointment and complete the study at this time. They will provide feedback about the 3D printed brace through a semi-structured interview (recorded using BCM Zoom Platform) and complete a survey (Qualtrics). They will return the brace, marking the end of the study.
Total duration of study participation ranges from 2 weeks - 6 weeks. The time commitment required from the participant is no more than 8 hours. The timelines are outlined below:
- Participant enrollment during appointment at Align Clinic (complete consent forms, demographic survey, baseline testing). Study-related activities will take approximately 30-60 minutes
- 3D printed brace fabrication. Nothing required of participants. Fabrication will take roughly 1-4 weeks
- Brace fitting. Participant will come to the office to be fit with the 3D-printed brace. Fitting will take roughly 1-4 hours
- Activity series in 3D printed brace. Will occur on the same day as the fitting. Testing will take approximately 30 minutes
- Follow-up appointment one week after the fitting. 3D printed brace is returned, marking the end of the study. Study activities (semi-structured interview, survey) will take 30-60 minutes.
Standard of care will be maintained throughout the study. The only activities outside of the standard of care are the semi-structured interview, study surveys, and performance of tasks. While the goal of the study is to elevate the 3D printed materials, the investigators will still be following the standard of care for 3D printing.
- Being tested
- 3D-printed scoliosis brace
- Keywords
- 3D-printed scoliosis brace, scoliosis brace, scoliosis bracing, 3D-printing
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
3D-printed scoliosis braceDevice
Scoliosis brace will be 3D printed using a Filament Innovations Icarus printer and the material CPX. There will be corrugations where extra strength is needed. The brace will be made using the same shape as the participant's current brace to minimize variables at play.
According to Sec. 890.3490 of the Code of Federal Regulations Title 21, scoliosis braces are Class I devices, requiring only general controls. This device is exempt from the premarket notification procedures in subpart E of part 807 of this chapter, subject to the limitations in § 890.9. The device is also exempt from the current good manufacturing practice requirements of the quality system regulation in part 820 of this chapter, with the exception of § 820.180, regarding general requirements concerning records and § 820.198, regarding complaint files.
| Study group | Role | What they receive |
|---|---|---|
| 3D-printed brace | Experimental | Enrolled participants will be fit with a 3D printed brace. The brace will be made using the exact same shape as their current brace. The fitting procedures will also remain the same. Receives: Device: 3D-printed scoliosis brace |
What is being measured
The primary outcome is the main question the study is designed to answer.
Perceived brace comfort
Participants will complete a series of tasks (sitting down, putting shoes on, stepping onto stool, etc.) in their current brace and in the 3D-printed scoliosis brace. Each task will be completed three times and researchers will be blinded to participant responses. A Wilcoxon signed-rank test will compare 3D printed brace comfort to baseline measures.
Measured: Comparing baseline comfort measures at enrollment (current brace) to comfort measures in 3D-printed brace at fitting (roughly 4 weeks after enrollment)
Secondary outcomes (1)
Semi-structured interview
A semi-structured interview will be performed to understand the differences between the two braces. Systematic coding procedures (e.g., open, axial, and selective coding) will be conducted by the research team.
Measured: Conducted at one-week follow-up appointment
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted21 Jan 2025
- Study start1 Apr 2025
- Primary completion31 Oct 2026 (estimated)
- Study completion31 Oct 2026 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (2)Papers the sponsor has linked to this study.
- Other trials for Scoliosis Idiopathic Adolescent TreatmentStudies of the same condition, open and under way.
- More trials run by Baylor College of MedicineThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Device feasibility
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Enrolment
- 5 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Baylor College of Medicine
- Sponsor type
- University, hospital or other
- Collaborators
- Scoliosis Research Society
- Responsible party
- Principal investigator, Megan Elizabeth Castille, Baylor College of Medicine
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06785207
- Sponsor's protocol ID
- H-55196
- Acronym
- 3DSCOLIBRACE
- Status last verified
- May 2026
- First submitted
- 16 Jan 2025
- Last updated
- 2 Jun 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Undecided
Publications
Nathan P, Chou SM, Liu G. A review on different methods of scoliosis brace fabrication. Prosthet Orthot Int. 2023 Aug 1;47(4):424-433. doi: 10.1097/PXR.0000000000000195. Epub 2023 Jan 31.
PubMed 36723398Ronca A, Abbate V, Redaelli DF, Storm FA, Cesaro G, De Capitani C, Sorrentino A, Colombo G, Fraschini P, Ambrosio L. A Comparative Study for Material Selection in 3D Printing of Scoliosis Back Brace. Materials (Basel). 2022 Aug 19;15(16):5724. doi: 10.3390/ma15165724.
PubMed 36013868
Study at a glance
From the registry record, last updated by the sponsor on 2 Jun 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Rethinking Rigidity: Development of a 3D-Printed Scoliosis Brace With Varying Flexibility
- ClinicalTrials.gov ID
- NCT06785207
- Acronym / sponsor ID
- 3DSCOLIBRACE / H-55196
- Keywords
- 3D-printed scoliosis brace, scoliosis brace, scoliosis bracing, 3D-printing
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 5 participants (estimated)
- Lead sponsor
- Baylor College of MedicineUniversity, hospital or other
- Collaborators
- Scoliosis Research Society
- Study start
- 1 Apr 2025 (actual)
- Primary completion
- 31 Oct 2026 (estimated)
- Study completion
- 31 Oct 2026 (estimated)
- First posted
- 21 Jan 2025 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Scoliosis bracing is an effective treatment method for idiopathic scoliosis, but only if worn consistently for many hours a day. Unsurprisingly, brace discomfort is a significant deterrent against treatment adherence. For decades, custom braces for idiopathic scoliosis have been fabricated using one of three materials - copolymer, polypropylene, or polyethylene. The application of the biomechanical principles behind bracing have improved over the years, but the materials have not. The investigators' goal is to expand fabrication options by testing a 3D-printed scoliosis brace with variable flexibility. The aim is to improve patients' perceived brace comfort.
After optimizing the brace design, the investigators will collect patient feedback about the design from currently braced participants. These participants understand what a standard brace feels like and will provide impactful feedback.
Detailed description
After optimizing the brace design, the investigators will collect patient feedback about the design from currently braced participants. Once a participant enrolls in the study, the 3D printed brace will be made using the exact same shape as their current brace. The standard fabrication process includes the following:
- Certified orthotist completes a full evaluation
- Taking a scan of the patient's body
- Modifying, or editing, the patient's body shape using Computer-Aided-Design and applying corrective pressures against the apex of the scoliotic curve
- Carving a positive foam model of the modified shape and thermoforming the polypropylene plastic over the positive foam model
These steps were already completed to make the participant's current brace, which has been deemed acceptable by their medical team, including the PI and Dr. Timothy Borden. To reduce the number of variables present, the 3D printed brace will be made using the exact same shape as their current brace. The only difference is the fabrication technique (step 4). Instead of carving a foam mode and thermoforming, the exact brace shape will be directly 3D printed. Therefore, no additional x-rays, scans, or measurements are required from the participants. The standard fabrication process and research activities are outlined in attachment titled "Fabrication Process Outline."
Once the 3D printed brace has been fabricated, the participant will come in to be fit with the brace. A standard fitting involves trimming the brace, adding straps, heating and flaring to improve comfort, and potentially adding padding. The PI is a scoliosis bracing specialist and will be the lead orthotist during the fitting process to ensure that best practices are followed.
Following the fitting, the participant will provide test out the 3D printed brace for comfort by performing a series of tasks. The activities will include the following: sitting in a chair, picking an item up from the floor while standing, picking an item up from the floor while sitting, stepping onto a stool, jogging in place for 10s, performing the hula hoop Wii-fit game, lying down on an exam table, and donning shoes. All data collection will take place via the survey platform Qualtrics.
If the participants feel comfortable in the brace and pass a skin check, the participants will then take the brace home and wear it for 1 week. They will return for the 1-week follow-up appointment and complete the study at this time. They will provide feedback about the 3D printed brace through a semi-structured interview (recorded using BCM Zoom Platform) and complete a survey (Qualtrics). They will return the brace, marking the end of the study.
Total duration of study participation ranges from 2 weeks - 6 weeks. The time commitment required from the participant is no more than 8 hours. The timelines are outlined below:
- Participant enrollment during appointment at Align Clinic (complete consent forms, demographic survey, baseline testing). Study-related activities will take approximately 30-60 minutes
- 3D printed brace fabrication. Nothing required of participants. Fabrication will take roughly 1-4 weeks
- Brace fitting. Participant will come to the office to be fit with the 3D-printed brace. Fitting will take roughly 1-4 hours
- Activity series in 3D printed brace. Will occur on the same day as the fitting. Testing will take approximately 30 minutes
- Follow-up appointment one week after the fitting. 3D printed brace is returned, marking the end of the study. Study activities (semi-structured interview, survey) will take 30-60 minutes.
Standard of care will be maintained throughout the study. The only activities outside of the standard of care are the semi-structured interview, study surveys, and performance of tasks. While the goal of the study is to elevate the 3D printed materials, the investigators will still be following the standard of care for 3D printing.
Study design
- Primary purpose
- Device feasibility
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| 3D-printed brace | Experimental | Device: 3D-printed scoliosis braceEnrolled participants will be fit with a 3D printed brace. The brace will be made using the exact same shape as their current brace. The fitting procedures will also remain the same. |
Who may qualify
- Ages
- 8 to 18 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child, Adult
Key inclusion criteria (9 listed)
- Have a diagnosis of juvenile idiopathic scoliosis or adolescent idiopathic scoliosis
- Have a Cobb angle between 20-40 degrees
- Are between ages 8-18
- Present as Risser 2+ on x-ray
- Currently wear a traditionally fabricated scoliosis brace
Key exclusion criteria (7 listed)
- Have a diagnosis other than juvenile idiopathic scoliosis or adolescent idiopathic scoliosis
- Have a Cobb angle outside the range of 20-40 degrees
- Present as Risser 0 or 1
- Do not currently wear a traditionally fabricated scoliosis brace
- Have poor adherence in their current brace
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| 3D-printed scoliosis braceScoliosis brace will be 3D printed using a Filament Innovations Icarus printer and the material CPX. There will be corrugations where extra strength is needed. The brace will be made using the same shape as the participant's current brace to minimize variables at play. According to Sec. 890.3490 of the Code of Federal Regulations Title 21, scoliosis braces are Class I devices, requiring only general controls. This device is exempt from the premarket notification procedures in subpart E of part 807 of this chapter, subject to the limitations in § 890.9. The device is also exempt from the current good manufacturing practice requirements of the quality system regulation in part 820 of this chapter, with the exception of § 820.180, regarding general requirements concerning records and § 820.198, regarding complaint files. | Device | 3D-printed brace |
Primary outcome
Perceived brace comfort
Time frame: Comparing baseline comfort measures at enrollment (current brace) to comfort measures in 3D-printed brace at fitting (roughly 4 weeks after enrollment)
Participants will complete a series of tasks (sitting down, putting shoes on, stepping onto stool, etc.) in their current brace and in the 3D-printed scoliosis brace. Each task will be completed three times and researchers will be blinded to participant responses. A Wilcoxon signed-rank test will compare 3D printed brace comfort to baseline measures.
1 secondary outcome
Semi-structured interview
Time frame: Conducted at one-week follow-up appointment
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 2 Jun 2026.
- Results publication: PubMed 36723398Nathan P, Chou SM, Liu G. A review on different methods of scoliosis brace fabrication. Prosthet Orthot Int. 2023 Aug 1;47(4):424-433. doi: 10.1097/PXR.0000000000000195. Epub 2023 Jan 31.
- Results publication: PubMed 36013868Ronca A, Abbate V, Redaelli DF, Storm FA, Cesaro G, De Capitani C, Sorrentino A, Colombo G, Fraschini P, Ambrosio L. A Comparative Study for Material Selection in 3D Printing of Scoliosis Back Brace. Materials (Basel). 2022 Aug 19;15(16):5724. doi: 10.3390/ma15165724.
- Individual participant dataSharing planned: Undecided
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
2 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing 3D-printed scoliosis brace in people with Scoliosis Idiopathic Adolescent Treatment, run by Baylor College of Medicine at 2 sites in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 9 inclusion and 7 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: looking for participants now, as of the sponsor's last update on 2 Jun 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 2 sites in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Megan EG Castille, MS (713-798-3098, megan.glahn@bcm.edu), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Perceived brace comfort (time frame: Comparing baseline comfort measures at enrollment (current brace) to comfort measures in 3D-printed brace at fitting (roughly 4 weeks after enrollment)). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT06785207, which also lists 2 linked publications.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 2 Jun 2026.