Study Stopped
Due to inability to recruit participants.
Exercise in Pediatric Autologous Stem Cell Transplant Patients
SCORE
2 other identifiers
interventional
24
1 country
2
Brief Summary
Hematopoietic stem cell transplantation is an intensive therapy used to improve survivorship and cure various oncologic diseases. However, this therapy is associated with high mortality rates and numerous negative side-effects. The recovery of the immune system is a special concern and plays a key role in the success of this treatment. In healthy populations it is known that exercise plays an important role in immune system regulation, but little is known about the role of exercise in the hematological and immunological recovery of children undergoing hematopoietic stem cell transplant. The Primary objective of this Randomized Controlled Trial is: study the effect of an exercise program on immune cell recovery in patients undergoing autologous stem cell transplantation. The Secondary objective is to determine if an exercise intervention might diminish the deterioration of quality of life, physical fitness, and the acquisition of a sedentary lifestyle. Methods Twenty-four participants treated for a malignancy with autologous stem cell transplant (5 to 18 years) in the Alberta Children's Hospital will be randomly assigned to an exercise or control group. The exercise group will participate in a two-phase exercise intervention (in and outpatient) from hospitalization until 10 weeks after discharge. The exercise program includes strength, flexibility and aerobic exercise. During the inpatient phase this program will be performed 5 times/week and will be supervised. The outpatient phase will combine a supervised session with two home-based exercise sessions with the use of the Wii device. The control group will follow the standard protocol without any specific exercise program. A range of outcomes, including quantitative and functional recovery of immune system, cytokine levels in serum, NK cells and their subset recovery and function, and gene expression of activating and inhibitory NK cell receptors, body composition, nutrition, quality of life, fatigue, health-related fitness assessment and physical activity levels will be examined, providing the most comprehensive assessment to date. Discussion We expect to find an improvement in the immunological recovery, quality of life, decreased acquisition of sedentary behavior and less fitness deconditioning.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable cancer
Started Jun 2012
Typical duration for not_applicable cancer
2 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
June 1, 2012
CompletedFirst Submitted
Initial submission to the registry
August 10, 2012
CompletedFirst Posted
Study publicly available on registry
August 16, 2012
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 1, 2014
CompletedStudy Completion
Last participant's last visit for all outcomes
October 1, 2014
CompletedOctober 26, 2016
October 1, 2016
2.2 years
August 10, 2012
October 24, 2016
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Hematological and Immunological Recovery
Assessment of the impact of the Exercise (EX) intervention on the immune recovery of pediatric autologous SCT patients will be based on four parameters (a) Recovery of different leukocyte cell subset (e.g., T cells, Natural killer cells, B cells, monocytes, neutrophils etc) in peripheral blood by flow cytometry, (b) Expression of activating and inhibitory Killer IRs by Gene expression analysis of 14 KIR genes will be done by RNA based real-time PCR analysis(c) Function of NK cells and their subsets by measuring in-vitro cytokine secretion and degranulation by different NK cell subsets (cytolytic and regulatory NK cells) on incubation with K-562 cell lines and (d) Levels of different pro-inflammatory and regulatory cytokines in serum using a bead-based array on Luminex.
This assessments will be performed at baseline, 7, 14, 28, 56, 84 and 180 days after stem cell transplantation (SCT)
Secondary Outcomes (1)
Quality of life (QOL)
Assessment will be completed at baseline, 30, 90 and 180 days after SCT
Other Outcomes (4)
Health-related fitness assessment
Assessment will be completed at baseline, 30 and 90 days after SCT
Physical activity levels
Assessment will be completed at baseline, 30, 90 and 180 days after SCT
Demographic and health assessment
This assessment will be perfomed at baseline, 15, 30, 60, 90 days after SCT
- +1 more other outcomes
Study Arms (2)
Exercise (EX)
EXPERIMENTALThis group will perform two phases of an EX program.
Standard Care
ACTIVE COMPARATORThis group will follow the standard care without any EX prescription.
Interventions
This study will examine the effect of two phases of an EX program on several health related outcomes in pediatric patient undergoing autologous SCT. The first phase of the EX program will be an inpatient intervention and will begin when the child is hospitalized undergoing conditioning therapy and will continue until discharge. The second phase will be a 10-week outpatient intervention, beginning once the child is discharged. We will utilize a mixed EX program, including supervised (at the University of Calgary) and home-based training incorporating the use of the Nintendo ® Wii device™ (Wii Fit, Wii Dance and Sports™ games).
This group will be under standard care without any EX intervention.
Eligibility Criteria
You may qualify if:
- autologous SCT at Alberta Children's Hospital (ACH) for malignancy
- age 5 to 18 years of age
- will be receiving myeloablative conditioning regimen
- no evidence of cardiac or pulmonary failure associated with treatment (SF≥28%, EF ≥ 50%)
- no functional nor cognitive limitation that would prohibit performance of the home-based training
- approval by treating oncologist for participants
- a parent or legal guardian must sign the consent form and
- children should express verbal assent to participate.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- University of Calgarylead
- Alberta Children's Hospitalcollaborator
Study Sites (2)
University of Calgary
Calgary, Alberta, T2N 1N4, Canada
Alberta Children's Hospital
Calgary, Alberta, T3B 6A8, Canada
Related Publications (1)
Chamorro-Vina C, Guilcher GM, Khan FM, Mazil K, Schulte F, Wurz A, Williamson T, Reimer RA, Culos-Reed SN. EXERCISE in pediatric autologous stem cell transplant patients: a randomized controlled trial protocol. BMC Cancer. 2012 Sep 10;12:401. doi: 10.1186/1471-2407-12-401.
PMID: 22963378DERIVED
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Nicole S Culos-Reed, Ph.D
University of Calgary Faculty of Kinesiology, Faculty of Medicine and Department of Psychosocial Resources, Tom Baker Cancer Centre
- PRINCIPAL INVESTIGATOR
Carolina Chamorro-Viña, Ph.D
Faculty of Kinesiology, University of Calgary.
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Ph.D, Associate Professor
Study Record Dates
First Submitted
August 10, 2012
First Posted
August 16, 2012
Study Start
June 1, 2012
Primary Completion
August 1, 2014
Study Completion
October 1, 2014
Last Updated
October 26, 2016
Record last verified: 2016-10