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ACTIVE NOT RECRUITING
NCT06824441
NA

Feasibility Usability & Acceptability Study: Symptom Reporting by Children Adolescents & Young Adults w/Cancer

Sponsor: Stanford University

View on ClinicalTrials.gov

Summary

The purpose of this project is to pilot test an electronically delivered symptom assessment tool Pediatric Patient-Reported Outcomes version of the Common Terminology Criteria for Adverse Events (Ped-PRO-CTCAE), completed by children/adolescents and young adults (AYAs) and caregivers and shared with their clinicians during an outpatient clinic visit, in preparation for a future test of intervention efficacy.

Official title: Symptom Reporting by Children, Adolescents and Young Adults With Cancer and Their Caregivers During a Clinic Visit: A Feasibility, Usability and Acceptability Study

Key Details

Gender

All

Age Range

7 Years - 21 Years

Study Type

INTERVENTIONAL

Enrollment

83

Start Date

2024-08-18

Completion Date

2026-10

Last Updated

2026-03-12

Healthy Volunteers

No

Interventions

BEHAVIORAL

Age- and Role-Specific Questionnaire Administration

Participants will be assigned a sequence number upon eligibility confirmation. The intervention consists of completing a series of questionnaires, as follows: Child/AYA/Caregiver Group: Pre-clinic Visit: 3 questionnaires (approximately 15-20 minutes total). Post-clinic Visit: 2 questionnaires (approximately 5-10 minutes total). Clinician Group: Post-clinic Visit: 2 questionnaires (approximately 5 minutes total).

Locations (1)

Stanford University

Palo Alto, California, United States