Trial · NCT07896135
Registered outcomes12
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
1 to 12 of 12
Download this page as JSON| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Postural Stability | Baseline (Pre-Intervention) | Postural stability and dynamic Limits of Stability (LOS) were assessed using the ProKin System. Across three maximum-effort trials with 60-second rest intervals, the software calculated: Mediolateral Excursion Limit (%), Anteroposterior Excursion Limit (%), Overall Excursion Area (mm2), Directional Control Index, and Trunk Displacement Angle (o), with the mean of three successful trials retained for statistical analysis. |
| Primary | Postural Stability | Week 8 (Post-Intervention) | Postural stability and dynamic Limits of Stability (LOS) were assessed using the ProKin System. Across three maximum-effort trials with 60-second rest intervals, the software calculated: Mediolateral Excursion Limit (%), Anteroposterior Excursion Limit (%), Overall Excursion Area (mm2), Directional Control Index, and Trunk Displacement Angle (o), with the mean of three successful trials retained for statistical analysis. |
| Primary | Lower Quarter Y-Balance Test (YBT-LQ) | Baseline (Pre-Intervention) | Dynamic balance was assessed using the Lower Quarter Y-Balance Test (YBT-LQ). Participants stood on one leg on the central platform and reached as far as possible with the contralateral leg in the anterior (AT), posteromedial (PM), and posterolateral (PL) directions while maintaining balance. The composite score for was calculated as: composite score (%) = \[AT + PM + PL maximal reach distances (cm)\] / \[3 × lower-limb length (cm)\] × 100. |
| Primary | Lower Quarter Y-Balance Test (YBT-LQ) | Week 8 (Post-Intervention) | Dynamic balance was assessed using the Lower Quarter Y-Balance Test (YBT-LQ). Participants stood on one leg on the central platform and reached as far as possible with the contralateral leg in the anterior (AT), posteromedial (PM), and posterolateral (PL) directions while maintaining balance. The composite score for was calculated as: composite score (%) = \[AT + PM + PL maximal reach distances (cm)\] / \[3 × lower-limb length (cm)\] × 100. |
| Secondary | Functional Gait Assessment Modified for Children | Baseline (Pre-Intervention) | Functional gait performance was assessed using the Functional Gait Assessment modified for Children (FGA-mC). The FGA-mC consists of 10-item assessment designed to evaluate higher-level gait performance under progressively challenging conditions. Higher scores indicate better functional gait performance. |
| Secondary | Functional Gait Assessment Modified for Children | Week 8 (Post-Intervention) | Functional gait performance was assessed using the Functional Gait Assessment modified for Children (FGA-mC). The FGA-mC consists of 10-item assessment designed to evaluate higher-level gait performance under progressively challenging conditions. Higher scores indicate better functional gait performance. |
| Secondary | Single Hop for Distance Test | Baseline (Pre-Intervention) | The Single Hop for Distance Test used to assess unilateral lower-limb functional performance, including forward propulsion and landing control. Hop distance was measured to the nearest 0.5 cm from the starting line to the posterior aspect of the heel at landing. To allow standardized comparisons, absolute hop distance (cm) was normalized to leg length and demonstrated as a percentage. |
| Secondary | Single Hop for Distance Test | Week 8 (Post-Intervention) | The Single Hop for Distance Test used to assess unilateral lower-limb functional performance, including forward propulsion and landing control. Hop distance was measured to the nearest 0.5 cm from the starting line to the posterior aspect of the heel at landing. To allow standardized comparisons, absolute hop distance (cm) was normalized to leg length and demonstrated as a percentage. |
| Secondary | Timed Up and Down Stairs Test | Baseline (Pre-Intervention) | Timed Up and Down Stairs Test was used to assess functional mobility. the subject was asked to stand 30 cm from the bottom of a 14-step flight of stairs (19.5-cm step height). The test score was the time in seconds from the "go" cue until the second foot returned to the bottom land |
| Secondary | Timed Up and Down Stairs Test | Week 8 (Post-Intervention) | Timed Up and Down Stairs Test was used to assess functional mobility. the subject was asked to stand 30 cm from the bottom of a 14-step flight of stairs (19.5-cm step height). The test score was the time in seconds from the "go" cue until the second foot returned to the bottom land |
| Secondary | Timed One-Legged Stance Test | Baseline (Pre-Intervention) | The Timed One-Legged Stance test was used to assess single-limb static balance and postural control. Timing began when the no stance foot left the floor and stopped if the participant removed the hands from the hips, looked down, touched the floor with the contralateral foot, or otherwise lost the test position. Performance was recorded in seconds, with longer times indicating better balance ability. |
| Secondary | Timed One-Legged Stance Test | Week 8 (Post-Intervention) | The Timed One-Legged Stance test was used to assess single-limb static balance and postural control. Timing began when the no stance foot left the floor and stopped if the participant removed the hands from the hips, looked down, touched the floor with the contralateral foot, or otherwise lost the test position. Performance was recorded in seconds, with longer times indicating better balance ability. |
Source ClinicalTrials.govtrials-2026-11-12-0.5.0
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
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