Targeting Caregivers to Enhance Health Behaviors in Pediatric Cancer Survivors
NCT ID: NCT02815982
Last Updated: 2018-09-20
Study Results
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View full resultsBasic Information
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COMPLETED
NA
106 participants
INTERVENTIONAL
2013-12-31
2016-12-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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NOURISH-T
The intervention aims to increase caregivers' self-efficacy for behavioral change, and facilitate an authoritarian approach to parenting. Behavioral strategies such as self-monitoring, contingency management, and stimulus control are integrated in these sessions. Further, because participatory experiences enhance overall intervention efficacy, these activities are incorporated throughout, including self-assessments, discussions and experiential activities. Homework is assigned between sessions so skills can be practiced. We also focus on the caregivers' relationship with everyone in the family, not just the "identified patient" or overweight child.
NOURISH-T
Overweight/obesity family intervention
Enhanced Usual Care
Caregivers randomized to the EUC will attend assessment sessions and an initial session moderated by an independent interventionist. The session addresses the role of diet and exercise in pediatric overweight. In addition, EUC caregivers receive nationally available print or web-based brochures on pediatric overweight on 2 occasions during the study so that similar (but not as intensive) information is provided in the intervention and EUC arms of the study. Participants also receive a booster phone call 2 months after the end of the intervention period.
Enhanced Usual Care
Publicly available overweight/obesity materials
Interventions
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NOURISH-T
Overweight/obesity family intervention
Enhanced Usual Care
Publicly available overweight/obesity materials
Eligibility Criteria
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Inclusion Criteria
* Mothers and fathers (biologic/adoptive/step parents/legal guardians) of pediatric cancer survivors
* 18 years or older
* Fluent in English
Pediatric Cancer Survivors
* Diagnosis of cancer
* between 5-13 years of age at study entry
* off active cancer treatment for 6 months to 4 years,
* reside with a participating caregiver
* able to engage in PA tailored to current medical status
* NOT taking medications that affect body weight, e.g., steroids within 6 months of enrollment
* at or above the 85th BMI %ile.
Exclusion Criteria
* are non-ambulatory
* do not reside with the PCS at least 50% of the time.
Pediatric cancer survivor
* relapse during the intervention
* taken a medication known to affect body weight such as oral steroids or antipsychotic medications within 6 months of enrollment
5 Years
13 Years
ALL
No
Sponsors
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University of Pittsburgh
OTHER
Johns Hopkins All Children's Hospital
OTHER
University of South Florida
OTHER
Responsible Party
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Principal Investigators
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Marilyn Stern, PhD
Role: PRINCIPAL_INVESTIGATOR
University of South Florida
Locations
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Johns Hopkins All Children's Hospital
St. Petersburg, Florida, United States
Children's Hospital of Pittsburgh
Pittsburgh, Pennsylvania, United States
Countries
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References
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Stern M, Ewing L, Davila E, Thompson AL, Hale G, Mazzeo S. Design and rationale for NOURISH-T: a randomized control trial targeting parents of overweight children off cancer treatment. Contemp Clin Trials. 2015 Mar;41:227-37. doi: 10.1016/j.cct.2014.12.018. Epub 2015 Jan 2.
Stern M, Bleck J, Ewing LJ, Davila E, Lynn C, Hale G, Mazzeo S. NOURISH-T: Targeting caregivers to improve health behaviors in pediatric cancer survivors with obesity. Pediatr Blood Cancer. 2018 May;65(5):e26941. doi: 10.1002/pbc.26941. Epub 2018 Jan 19.
Other Identifiers
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