St. Jude Children's Research Hospital
Memphis, Tennessee, 38105, United States
NCT Number: NCT01047020
The primary goal of this study is to provide comprehensive and objective information on impairments of musculoskeletal health, sensory function, and fitness among a large group of childhood ALL survivors, and to define high risk groups by assessing treatment factors that contribute to impaired function. This study includes a direct, objective evaluation of musculoskeletal function, sensory capacity, fitness, and physical activity patterns among adults who were treated for childhood ALL at St. Jude Children's Research Hospital (SJCRH) between 1980 and 1999. Among 899 ALL survivors, all of whom are eligible for an institutionally funded clinical study of medical late effects, the study will recruit 364 to participate in our evaluations. The study will also recruit 364 individuals for a comparison group, frequency matching on race/ethnicity, age and gender.
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Notify Me18 year and older
All sexes
Observational
Memphis, Tennessee, 38105, United States
The study will focus on the following primary objectives:
The study will focus on the secondary objectives:
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
(ALL survivors):
Exclusion criteria
(ALL survivors):
Inclusion criteria
(Comparison Group)
Exclusion criteria
(Comparison Group)
Time frame: Day 1-2
Time frame: Day 1-7
Time frame: Day 1-7
Time frame: Day 1-7
St. Jude Children's Research Hospital
Other
Motor Proficiency And Physical Activity in Adult Survivors of Childhood ALL
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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