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Childhood Cancer clinical trials

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NCT ID: NCT02959086 Recruiting - Childhood Cancer Clinical Trials

Shanghai Epidemiology Study for Adolescents and Children With Cancer

Start date: January 2002
Phase:
Study type: Observational [Patient Registry]

The purpose of this study is to describe the morbidity, mortality, disability and survival rate in Shanghai adolescents and children with cancer diagnosed since January 2002.

NCT ID: NCT01772862 Recruiting - Childhood Cancer Clinical Trials

Rehabilitation Including Social and Physical Activity in Children and Teenagers With Cancer

RESPECT
Start date: January 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether early rehabilitation intervention including individualized physical training and social activities with a class mate at two weeks intervals at the ped.onc. center will increase children with cancer's level of physical performance

NCT ID: NCT01772849 Recruiting - Childhood Cancer Clinical Trials

Rehabilitation Including Social Activity and Education in Children and Teenagers With Cancer

RESPECT-EDU
Start date: January 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether early rehabilitation intervention including educational and social activities with a class mate at two weeks intervals at the ped.onc. center will increase children with cancer's level of education performance.

NCT ID: NCT01742325 Recruiting - Childhood Cancer Clinical Trials

The Effect of Walking Intervention on Sleep Related Symptom Distress in Pediatric Oncology Patients

Start date: January 2010
Phase: N/A
Study type: Interventional

Specific aims: Control group(2010/1~2011/6): Aim 1: Describe the patterns of "fatigue, sleep disturbance, and pain" in children with cancer from perspectives of children and their parents over the course of one cycle (five days) of inpatient chemotherapy (CXT). Aim 2: Determine, at various time points (during they are hospitalization various four times), the associations between fatigue, sleep disturbance, and pain over the course of four cycles (there are five days in each cycle) of CTX in children with cancer. Aim 3: Examine the associations between a symptom cluster of fatigue, sleep disturbance, pain, child reported Quality of Life for Children with Cancer (QOLCC), parent reported uncertainty and QOL, and biomarkers over the course of four cycles of CXT in children with cancer. Intervention group(2011/7~2012/12): Aim 4: To test an intervention program (two 20-minute sessions of walking around the nurse's station daily, five days a cycle) to reduce the symptoms of fatigue and pain and increase quality of sleep.

NCT ID: NCT01491230 Recruiting - Childhood Cancer Clinical Trials

Neutrophil Extracellular Traps Formation Post-hematopoietic Stem Cell Transplantation

NETs post HSCT
Start date: December 2011
Phase: N/A
Study type: Observational

Identifying the post-transplantation phase wherein neutrophils recover their ability to release NETs could shed new light on the mechanism responsible for the increased susceptibility to infection among these patients and aid in improving their prophylactic antimicrobial treatment. Therefore, we aim to examine neutrophil extracellular traps (NETs) formation, in relation to other neutrophil functions like chemotaxis, superoxide production, hydrogen peroxide production, and the presence of myeloperoxidase, in pediatric patients undergoing autologous and allogeneic hematopoietic stem cell transplantation (HSCT).

NCT ID: NCT00684580 Recruiting - Childhood Cancer Clinical Trials

Protocol For Collecting Data On Patients With Childhood Cancer

Start date: June 8, 2000
Phase:
Study type: Observational

Progress in the development of curative therapy for pediatric malignancies has resulted in increasing numbers of long-term childhood cancer survivors. This protocol is a means to provide continuing review of outcome and late toxicity for all patients actively being treated and previously treated for childhood cancer at St. Jude Children's Research Hospital.