Actively Recruiting

Phase Not Applicable
Age: 15Years - 29Years
All Genders
NCT05958316

Heuristic Tool To Improve Symptom Self-Management in Adolescents and Young Adults With Cancer

Led by Virginia Commonwealth University · Updated on 2026-04-13

126

Participants Needed

5

Research Sites

190 weeks

Total Duration

On this page

Sponsors

V

Virginia Commonwealth University

Lead Sponsor

N

National Cancer Institute (NCI)

Collaborating Sponsor

AI-Summary

What this Trial Is About

Determine the effects of the Computerized Symptom Assessment Tool (C-SCAT) versus usual care on the primary outcomes of self-efficacy for symptom management and symptom self-management behaviors

CONDITIONS

Official Title

Heuristic Tool To Improve Symptom Self-Management in Adolescents and Young Adults With Cancer

Who Can Participate

Age: 15Years - 29Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Has received at least 1 cycle of cancer treatment and is within 3 months of initial cancer diagnosis
  • Receiving regularly scheduled cancer treatment and will be receiving at least three more cycles
  • Reports at least 1 symptom related to cancer and/or its treatment
  • Able to speak, read, and write English as required for completion of the C-SCAT and study measures
Not Eligible

You will not qualify if you...

  • Cognitive and/or physical inability to complete study measures.

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Trial Site Locations

Total: 5 locations

1

Children's Mercy Hospital

Kansas City, Missouri, United States, 64108

Actively Recruiting

2

University of Utah Huntsman Cancer Institute (HCI)

Salt Lake City, Utah, United States, 84112

Actively Recruiting

3

University of Utah Primary Children's Hospital

Salt Lake City, Utah, United States, 84113

Actively Recruiting

4

Virginia Commonwealth University

Richmond, Virginia, United States, 23298

Actively Recruiting

5

Seattle Children's Hospital @ University of Washington

Seattle, Washington, United States, 98105

Active, Not Recruiting

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Research Team

G

Grace Hodges

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

2

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