RecruitingNot ApplicableNCT05958316

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

A Randomized Controlled Trial Using a Heuristic Tool To Improve Symptom Self-Management in Adolescents and Young Adults With Cancer


Sponsor

Virginia Commonwealth University

Enrollment

126 participants

Start Date

Jan 4, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

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


Eligibility

Min Age: 15 YearsMax Age: 29 Years

Inclusion Criteria4

  • 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

Exclusion Criteria1

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

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

BEHAVIORALComputerized Symptom Capture Tool (C-SCAT) Intervention

The C-SCAT includes the 32 symptoms from the Memorial Symptom Assessment Scale (MSAS). Users select symptoms they have experienced over the past week, rate each symptom's severity and distress, and name a perceived cause. They then identify temporal and causal relationships between symptoms using lines and arrows, designate groups, i.e., "clusters" of symptoms, and give a name to each cluster. They are asked the reason for a symptom's designation as a priority symptom and what they do to alleviate that symptom. Next, they are asked to designate a priority cluster and finally, to confirm whether the image accurately reflects their symptom experience. Then, at the clinic visit, the AYA shares the visual image with the HCP, and more importantly, their priority symptoms, which can facilitate the symptom discussion. The C-SCAT intervention group will complete the C-SCAT prior to each of three encounters with their health care providers (HCPs).

BEHAVIORALUsual Care Control

Usual care is defined as the usual approach to assessing symptoms during the HCP encounter. To provide attentional control to the usual care control group and prevent disproportionate attrition from that group, study staff will contact participants three times during the intervention period (approximately 3 months) when they are in for a scheduled clinic visit and communicate the following: 1) express appreciation for ongoing study participation; 2) ask how everything is going with their treatment; 3) ask if anything has changed with their treatment plan since the last study visit; and 4) confirm continued participation in the study.


Locations(5)

Children's Mercy Hospital

Kansas City, Missouri, United States

University of Utah Huntsman Cancer Institute (HCI)

Salt Lake City, Utah, United States

University of Utah Primary Children's Hospital

Salt Lake City, Utah, United States

Virginia Commonwealth University

Richmond, Virginia, United States

Seattle Children's Hospital @ University of Washington

Seattle, Washington, United States

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT05958316


Related Trials