ClinicalTrials.Veeva

Menu

BRAVE: Building Resilience and Values Through E-health

Stanford University logo

Stanford University

Status

Completed

Conditions

Survivorship

Treatments

Other: Online survey questionnaire

Study type

Interventional

Funder types

Other

Identifiers

NCT05227599
IRB-55183

Details and patient eligibility

About

The purpose of this study is to determine the feasibility and acceptability of tracking survivors' and their caregivers, stressors, affect, and symptoms using an electronic diary method, in the time period surrounding their routine check- up with their oncologist.

Enrollment

56 patients

Sex

All

Ages

11 to 25 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. 11-25 years old
  2. previously received a pediatric cancer diagnosis and treatment for such
  3. completed cancer treatment <5 years ago, in remission
  4. Own a smart phone or tablet
  5. are English proficient

Exclusion criteria

  • no cognitive, motor, or sensory deficits that could preclude completion of study measures.

Trial design

Primary purpose

Supportive Care

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

56 participants in 1 patient group

Daily Diary Method Cohort
Other group
Description:
Participants will be asked to complete a self-report questionnaire that has been validated to assess daily affect. There are 5 items assessing positive affect (joyful, cheerful, happy, lively, proud) and 5 items assessing negative affect (miserable, mad, afraid, scared sad). The respondent is asked to rate these 10 different feelings on a 5-point Likert scale from 1, "not much or not at all" to 5, "a lot."
Treatment:
Other: Online survey questionnaire

Trial contacts and locations

1

Loading...

Central trial contact

Sarah Webster

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems