Easing Scan Anxiety in Pediatric Oncology Caregivers Through Meditation-based Programs

NCT07420101 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 160

Last updated 2026-03-19

No results posted yet for this study

Summary

"Scanxiety" is a term coined to describe anxiety related to imaging during cancer treatment and has not been robustly studied in pediatric oncology caregivers. Mindfulness-based Stress Reduction (MBSR) is a meditation-based program that offers a non-pharmacologic approach to managing stress. The main purposes of this study are two-fold: 1). to determine if scanxiety exists in the caregivers of pediatric oncology patients and 2.) if scanxiety is found, does the implementation of a mindfulness program help to improve caregiver anxiety related to imaging.

Conditions

  • Caregiver Anxiety
  • Caregiver Anxiety Related to Cancer Imaging
  • Pediatric Oncology

Interventions

OTHER

Mindful Module Caregiver Packet

If Scanxiety was identified, patient's caregiver will receive the Mindful Module Caregiver Packet. The intervention group will receive the daily module on Days 1-7; Day 7 being the day before scan. At the end of the module (Day 7), they will be directed to two surveys (STAI and Feasibility of the Program).

Sponsors & Collaborators

  • Connecticut Children's Medical Center

    collaborator OTHER
  • UConn Health

    collaborator OTHER
  • Kimberley Roche

    lead OTHER

Principal Investigators

  • Kimberley Roche, MSN, PPCNP-BC, APRN · Connecticut Children's Medical Center

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2026-02-01
Primary Completion
2027-02-01
Completion
2027-02-01

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07420101 on ClinicalTrials.gov