Clinical Trials Directory

Trials / Completed

CompletedNCT05293743

Novel Dynamic Foot Abduction Bar for Treatment of Clubfoot

Development and Evaluation of Novel Dynamic Bar for Foot Abduction Brace for Clubfoot Treatment

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
17 (actual)
Sponsor
The Hospital for Sick Children · Academic / Other
Sex
All
Age
1 Year – 3 Years
Healthy volunteers
Accepted

Summary

The goal of this clinical trial is to evaluate a new Dynamic Bar for foot abduction bracing for clubfoot treatment. The main questions that this study aims to answer are: * How easy is it to recruit and retain participants for a randomized-controlled effectiveness trial of a novel foot abduction bar? * How does parental perception of child comfort in the Dynamic Bar compare to parental perception of child comfort in standard bars? * How does patient tolerance of the Dynamic Bar compare patient tolerance of standard bars? * How effective is the Dynamic Bar at preventing clubfoot recurrence during the bracing phase when the brace is worn as prescribed for a 30-day trial period? Each participant will be randomized into one of two arms: the experimental arm or the control arm. For the first 30 days, the experimental arm will wear the new Dynamic Bar with standard boots and the control arm will continue wearing their standard bar. After this 30-day period, the experimental arm will return to wearing their standard bar.

Detailed description

This is an assessor-blinded randomized feasibility trial assessing the feasibility of conducting a large-scale clinical trial to evaluate the effectiveness of a new dynamic bar for foot abduction bracing for clubfoot treatment. Feasibility will be determined by the ability to recruit patients within the goal study period and to retain participants. Eligible patients must have a well-corrected idiopathic clubfoot (Pirani Score ≤ 0.5) and be in the minimum 12 hours per day bracing stage of the Ponseti clubfoot treatment protocol. The overall study period will be 90 days in length. For the first 30 days, the experimental cohort will wear the new Dynamic Bar (DB) with standard ankle-foot orthoses (boots) and the control cohort will continue wearing their Standard Bar (SB). After this 30-day period, the experimental cohort will return to wearing their SB. All patients will be evaluated on Day 0, Day 7, Day 30, and Day 90 of the study period to monitor for recurrence of the clubfoot deformity, complications of brace wearing, to submit brace wear logs, and to complete parent-reported questionnaires regarding their perceptions of the Foot Abduction Brace (FAB) and their child's comfort. A minimum of 10 patients per arm will be recruited. A temperature sensor will be added in each participant's boots during the 90-day study period to objectively measure time of brace wear. It is hypothesized that when patients are wearing the DB, they will experience higher brace tolerance defined as increased wear time of the brace as measured by the temperature sensors, and higher comfort levels as reported by parents, without an increase in clubfoot deformity recurrence compared to the SB. Most patient information that will be reviewed in this study is data being collected and stored per the REB-approved Clubfoot Research Registry protocol (REB #1000053919). All patients enrolled in study this will also be enrolled in Clubfoot Research Registry, if not already enrolled. The novel DB is designed by the research team and allows independent movement of the knees and hips while maintaining a corrective position of the foot.

Conditions

Interventions

TypeNameDescription
DEVICEFoot abduction bracing for clubfoot with novel Dynamic BarAfter Ponseti treatment of serial casting and tenotomy for clubfoot, patients are braced full time x 3 months then night time until age 5. This study compares standard bars in a foot abduction brace to our novel Dynamic Bar. This group uses the Dynamic Bar.
DEVICEFoot abduction bracing for clubfoot with Standard BarAfter Ponseti treatment of serial casting and tenotomy for clubfoot, patients are braced full time x 3 months then night time until age 5. This study compares standard bars in a foot abduction brace to our novel Dynamic Bar. This group uses the Standard Bar.

Timeline

Start date
2022-08-17
Primary completion
2023-05-24
Completion
2023-05-24
First posted
2022-03-24
Last updated
2025-05-22
Results posted
2024-11-25

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT05293743. Inclusion in this directory is not an endorsement.