Targeting Caregivers to Enhance Health Behaviors in Pediatric Cancer Survivors

Not Applicable

Completed

Conditions: Cancer
Obesity

Interventions: Behavioral: Enhanced Usual Care
Behavioral: NOURISH-T

Registration Number: NCT02815982

Lead Sponsor: University of South Florida

Brief Summary: This purpose of this pilot study is to investigate the feasibility of and optimal time post cancer treatment to offer caregivers a new health behavior change intervention (NOURISH-T), as well as assess its preliminary efficacy on specific child health behaviors. The study will also explore whether caregivers NOURISH-T exhibit more improvements than caregivers in EUC (standard care).

Detailed Description: Approximately 40% of off-treatment pediatric cancer survivors (PCS) are overweight or obese, which increases their risk for negative long-term physical health complications. Consistent with the Institute of Medicine's (IOM) emphasis on patients transitioning from treatment to cancer survivorship and increasing long-term healthy behaviors in these survivors, we conducted a pilot RCT to address the increasing overweight/obesity rates among PCS by targeting their caregivers as agents for PCS behavior change. We focused on parents' behaviors, attitudes and roles in promoting healthier eating and physical activity (PA) in PCS and adapted an evidence-informed, manualized parent intervention - NOURISH - found to be effective for parents of overweight and obese children and adolescents in reducing child and adolescent BMI. We adapted NOURISH for caregivers of 5 - 13 year old PCS (6 months -4 years off active cancer treatment). Our pilot feasibility RCT - NOURISH-T (Nourishing Our Understanding of Role modeling to Improve Support for Healthy Transitions) evaluates: 1) the preliminary feasibility efficacy of NOURISH-T for PCS, compared with an Enhanced Usual Care (EUC) control condition, and 2) factors to consider to improve future adaptations of the intervention. The project enrolled caregivers of PCS at two pediatric oncology clinics into the 6-week intervention (or EUC) with assessments of both caregivers and PCS occurring pre- and post-6 weeks of intervention, and at a 4-month follow-up. In comparison to EUC, we hypothesized that caregivers and PCS assigned to the NOURISH-T condition would show greater improvements in dietary intake, physical activity, and in anthropometric health indicators over time.

Recruitment & Eligibility

Status: COMPLETED

Sex: All

Target Recruitment: 106

Inclusion Criteria

Caregivers

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

Caregivers

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

Study & Design

Study Type: INTERVENTIONAL

Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Enhanced Usual Care	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.
NOURISH-T	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.

Primary Outcome Measures

Name	Time	Method
Satisfaction and Exit Survey Composite Scale Score -- ONLY CAREGIVERS COMPLETED THIS MEASURE	6 weeks	At the end of the final session (6-sessions), caregivers completed a likert-type survey assessing what they liked/disliked about the intervention, as well as what was/was not useful or helpful in reaching health goals. Eleven items were summed to obtain a total continuous composite satisfaction/liking score. Each item was measured on a likert scale ranging from strongly disagree (=1) to strongly agree (=5). The scale sum score ranged from 11 to 55 with higher scores indicating greater satisfaction with the intervention. More specifically, the higher the score, the more useful the caregiver thought the intervention and the more they liked participating in the intervention. Lower scores indicate that the caregiver thought the program was not useful and they did not like participating.

Secondary Outcome Measures

Name	Time	Method
Automated Self-administered 24-Hour Dietary Recall (ASA 24) -- CAREGIVERS ONLY MEASURE	Pre-Intervention, Post-Intervention (6-weeks), Follow-up (4 Months)	A 24-hour recall was completed by caregivers using the Automated Self-administered 24-Hour Dietary Recall-2011 (adult version) at pre-intervention, post-intervention (6-weeks) and at 4 months follow-up. The outcome was measured as the number of calories consumed over 1-day. Caregivers reported detailed information on the foods consumed and quantity including the method used for preparation, portion sizes, and where the food was purchased using visual cues in the previous day through the ASA24 website (https://asa24.nci.nih.gov/). The website reported the total number of calories consumed based on the data input.
Child Sugar Sweet Beverage and Fast Food Intake Scale Sum Score -- ONLY Pediatric Cancer Survivors (PCS) Assessed on This Measure	Pre-Intervention, Post-Intervention (6-weeks), Follow-up (4 Months)	This 8-item questionnaire was completed by the pediatric cancer survivor and assessed child intake of sugar sweetened beverages, breakfast and dinner habits, as well as frequency of fast food intake. The sum score represents the total number of sugary beverages consumed and the number of times consuming fast food in the prior week. Higher scores indicate greater consumption of sugary beverages and fast food in the prior week. The sum score could range from 0 and has no upper limit.
Child Feeding Questionnaire Sum Score -- ONLY CAREGIVERS COMPLETED THIS MEASURE	Pre-Intervention, Post-Intervention (6-weeks), Follow-up (4 Months)	This 31-item questionnaire assesses parental approaches to and attitudes about feeding their children. Sub-scales include concerns about child weight, monitoring, restriction, and pressure to eat. The sum score of the Likert items ranged from 31 to 155 with higher scores indicating greater perceived concern, monitoring, restriction and pressure to eat.
Parent BMI Score -- CAREGIVER MEASURE	Pre-Intervention, Post-Intervention (6-weeks), Follow-up (4 Months)	Measured at the clinic via standardized equipment.
Number of Daily Steps Averaged Over a Week for Caregivers -- CAREGIVER MEASURE	Pre-Intervention, Post-Intervention (6-weeks), Follow-up (4 Months)	PCS and caregivers were trained to wear a piezoelectric, computer downloadable pedometer consecutively for 7 days prior to the pre- and post- intervention and 4 months post-intervention assessments to assess frequency of daily steps. The scale was measured as the continuous number of daily steps averaged over a week.
Number of Daily Steps Averaged Over a Week -- ONLY Pediatric Cancer Survivors (PCS) Assessed	Pre-Intervention, Post-Intervention (6-weeks), Follow-up (4 Months)	PCS and caregivers were trained to wear a piezoelectric, computer downloadable pedometer consecutively for 7 days prior to the pre- and post- intervention and 4 months post-intervention assessments to assess frequency of daily steps. The scale was measured as the continuous number of daily steps averaged over a week.
Parent Waist to Hip Ratio -- CAREGIVER MEASURE	Pre-Intervention, Post-Intervention (6-weeks), Follow-up (4 Months)	Measured at the clinic via standardized equipment
Child Waist to Hip Ratio -- ONLY Pediatric Cancer Survivors (PCS) ASSESSED	Pre-Intervention, Post-Intervention (6-weeks), Follow-up (4 Months)	Measured at the clinic via standardized equipment.
Child BMI Percentile -- ONLY Pediatric Cancer Survivors (PCS)	Pre-Intervention, Post-Intervention (6-weeks), Follow-up (4 Months)	Continuous child BMI percentile as a function of gender and age. This measure was obtained via the PCS medical chart.

Trial Locations

Locations (2): Children's Hospital of Pittsburgh
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Pittsburgh, Pennsylvania, United States
Johns Hopkins All Children's Hospital
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Saint Petersburg, Florida, United States