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The Effects of Ankle Foot Orthoses on Gait Efficiency in Children With Acute Lymphoblastic Leukemia and Foot Drop

Not Applicable
Terminated
Conditions
Foot Drop
Acute Lymphoblastic Leukemia
Interventions
Device: AFO Device
Registration Number
NCT01001390
Lead Sponsor
St. Jude Children's Research Hospital
Brief Summary

This study is designed to see if children with acute lymphoblastic leukemia who have developed foot drop during treatment for their leukemia consume less oxygen when walking with or without an ankle brace designed to support their foot during walking. In this study children with foot drop are asked to walk for six minutes with and without brace on their ankle. During each walk, the amount of oxygen used is measured. The child wears a face mask which is attached to a device that records how much oxygen they use. The amount of oxygen used during the walk with the brace on will be compared to the amount of oxygen used with the brace off.

Detailed Description

1. This study will determine the impact of Ankle Foot Orthoses (AFO) wear on gait efficiency in children with ALL and Chemotherapy-Induced Peripheral Neuropathy (CIPN).

2. The study hypothesizes that children with CIPN will have lower net oxygen consumption during the six minute walk test while wearing AFO as compared to their net oxygen consumption during a six minute walk test while not wearing AFO.

3. The study will assess whether gait efficiency while using an AFO persists after one month of use.

4. The study will hypothesize that the benefits of AFO use on gait efficiency persist after one month of wear.

Recruitment & Eligibility

Status
TERMINATED
Sex
All
Target Recruitment
2
Inclusion Criteria
  1. Research participant is diagnosed with childhood ALL and currently being treated on the TOTAL XVI protocol at St. Jude Children's Research Hospital (SJCRH)
  2. Research participant is from 6 to 18 years of age at the time of the scheduled evaluation
  3. Research participant has chemotherapy-induced peripheral neuropathy resulting in foot drop
  4. Research participant will be receiving AFO
  5. Research participant has a hemoglobin level greater than 8 g/dL and a platelet count above 50 x 109/L
Exclusion Criteria
  1. Participant has Down Syndrome or other known congenital developmental delays
  2. Participant has a platelet count lower than 50 x 109/L and a hemoglobin level less than 8 g/dL
  3. Participant has a lower extremity amputation, congenital deformity of the lower limb or an acute fracture of the lower limb
  4. Participant has symptomatic osteonecrosis in the lower extremities

Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Arm && Interventions
GroupInterventionDescription
Group OneAFO DeviceGroup one will take a six minute walk test with AFO device, and after a rest of fifteen minutes, they will take another six minute walk test without AFO, with similar speed to the previous test.
Group TwoAFO DeviceGroup two will take a six minute walk test without AFO device, and after a rest of fifteen minutes, they will take another six minute walk test with AFO, with similar speed to the previous test.
Primary Outcome Measures
NameTimeMethod
Net Oxygen Consumption During the Six Minute Walk Test Among Study Participants Under the Two Walking Conditions, With and Without AFO.Baseline

Net oxygen consumption is calculated by the formula: \[net oxygen consumption = walking oxygen consumption - sitting oxygen consumption\], then adjusted by total mass in kg, including body mass, the mass of the socks, appropriate shoes, helmet, mouth piece system, and for the with AFO trials, the mass of the brace.

Secondary Outcome Measures
NameTimeMethod
Number of Participants With Improvement in Gait Efficiency While Using an AFOOne month after baseline evaluation

The difference of net oxygen consumption between wearing AFO and without wearing AFO (difference = wearing AFO - without wearing AFO) will be compared between the baseline study and one month later by using repeated measures analysis in which the effect of time will be tested controlling for other confounding variables.

Trial Locations

Locations (1)

St. Jude Children's Research Hospital

🇺🇸

Memphis, Tennessee, United States

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