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Clinical Trials/NCT01171599
NCT01171599
Completed
Not Applicable

PACE-CALL: A Weight Control Intervention for Survivors of Childhood Leukemia

University of California, San Diego1 site in 1 country12 target enrollmentAugust 2008

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Obesity
Sponsor
University of California, San Diego
Enrollment
12
Locations
1
Primary Endpoint
Acceptability and Usability of a Web & Text Message Based Intervention through Qualitative Feedback from Focus Groups
Status
Completed
Last Updated
13 years ago

Overview

Brief Summary

The purpose of this National Cancer Institute (NCI) funded study is to develop and test the acceptability and usability of a web & text message based weight loss intervention for childhood acute lymphoblastic leukemia (ALL) survivors. Childhood cancer survivors ages 7 - 18 will provide feedback during focus groups on a web and text message based program that was developed.

Detailed Description

This is a two year study to develop a predominantly web-based behavioral assessment and intervention program (PACE-CALL) that will provide individual assessment and tailoring of a behavioral intervention for adolescent children Acute Lymphoblastic Leukemia (ALL) survivors and their families. In addition, we are conducting formative research to adapt the abovementioned program to children and adolescents aged 7 - 18 who survived any cancer. Focus Groups: Web-Based \& Text Message Intervention Feedback Two focus groups will be conducted with adolescent cancer survivors and their families, to assess the usability and acceptability of the web-based intervention, focus groups will be conducted. The two focus groups will last 2 hours with 6-8 people in each group: one focus group with youth \& adolescents (age 7 - 18 who are representative of the target population to determine the appropriateness of the web-based intervention one focus group with the parents of the children in the focus group mentioned above (it will occur at the same time). All focus groups will begin with an overview of the study and description of the web-based intervention components. Focus group participants will see sample web pages and may be asked to provide feedback on some or all of the following: Youth, Adolescent or Parent: * How does the web-based and text message based intervention address issues faced by children who have survived cancer? * What do you like about the web-based intervention? What do you not like about the web-based intervention? What would you change about the web-based intervention? * What do you like about the text messages? What do you not like about the text messages? * Would you want to join a program like this? Why or why not? * If you were to be in this program, how often would you log on to the web-based intervention? How often would you want to receive text messages? * What are some of the barriers to joining a program like this?

Registry
clinicaltrials.gov
Start Date
August 2008
End Date
August 2011
Last Updated
13 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Are 7 - 18 years
  • Provide assent and have a legal guardian that will participate and provide parental permission/consent
  • Are a cancer survivor (off treatment for two years)
  • Are overweight or obese (85th percentile BMI (Body Mass Index) for age and gender)

Exclusion Criteria

  • Have any of the following comorbidities of obesity that require immediate sub-specialist referral including pseudotumor cerebri, sleep apnea, and obesity hypoventilation syndrome

Outcomes

Primary Outcomes

Acceptability and Usability of a Web & Text Message Based Intervention through Qualitative Feedback from Focus Groups

Time Frame: 2-hour focus group

The primary outcome is to develop a web and text message based weight loss intervention that will provide individual assessment and tailoring of a behavioral intervention for ALL survivors. In order to test the acceptaibility and usability of the website and text message program, focus groups will be conducted with cancer survivors to provide feedback on the program.

Study Sites (1)

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