Clinical Trials Directory

Trials / Active Not Recruiting

Active Not RecruitingNCT06824441

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

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

Status
Active Not Recruiting
Phase
N/A
Study type
Interventional
Enrollment
83 (actual)
Sponsor
Stanford University · Academic / Other
Sex
All
Age
7 Years – 21 Years
Healthy volunteers
Not accepted

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.

Conditions

Interventions

TypeNameDescription
BEHAVIORALAge- and Role-Specific Questionnaire AdministrationParticipants 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).

Timeline

Start date
2024-08-18
Primary completion
2026-10-01
Completion
2026-10-01
First posted
2025-02-13
Last updated
2026-03-12

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT06824441. Inclusion in this directory is not an endorsement.