Purpose

This is a prospective, observational cohort study of pediatric patients ages 2-12 undergoing radiation therapy at MD Anderson Cancer Center.

Conditions

Eligibility

Eligible Ages
Between 2 Years and 12 Years
Eligible Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

To be eligible to participate in this study, an individual must meet all of the following criteria: - Provision of signed and dated informed consent from a parent or legal guardian. - For children age 7 and older, provision of informed assent in addition to parental consent, consistent with institutional guidelines. - Stated willingness of parent/guardian and child (as appropriate) to comply with study procedures (i.e., observation during scheduled radiation therapy appointments). - Male or female, ages 2-12 years. - Scheduled to undergo radiation therapy at MD Anderson Cancer Center.

Exclusion Criteria

An individual who meets any of the following criteria will be excluded from participation in this study: - Has already completed the simulation session for radiation therapy prior to enrollment. - Declines parental consent or, when applicable, child assent.

Study Design

Phase
Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Recruiting Locations

More Details

Status
Recruiting
Sponsor
M.D. Anderson Cancer Center

Study Contact

Susan L McGovern, MD, PHD
(713) 563-2336
slmcgove@mdanderson.org

Detailed Description

Primary Objective: The primary objective of this study is to characterize procedural anxiety trajectories in pediatric patients ages 2-12 undergoing radiation therapy. Anxiety will be measured using the Modified Yale Preoperative Anxiety Scale Short Form (mYPAS-SF) at standardized clinical milestones (simulation, first week of treatment, mid-treatment, and final treatment week). Secondary Objectives: Secondary objectives are to explore associations between observed anxiety levels and treatment-related contextual factors, including: - Treatment fraction number - Anesthesia use - Child-life support - Parent or caregiver presence - Waiting times of 30 minutes or longer - Time of day

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.