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Digital Phenotyping for Psychosocial Screening in Adolescents and Young Adults With Cancer

Stanford University logo

Stanford University

Status

Enrolling

Conditions

Adolescents
Cancer

Treatments

Behavioral: Ecological Momentary Assessment (EMA) via My Personal Health Dashboard (MyPHD) Smartphone App
Device: Device

Study type

Interventional

Funder types

Other

Identifiers

NCT07220343
IRB-73748

Details and patient eligibility

About

The overall goal of the proposed study is to use digital phenotyping to identify and triage at-risk patients and accelerate access to critical mental health services.

Enrollment

25 estimated patients

Sex

All

Ages

10 to 25 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 10-25 years old
  • Recent cancer diagnosis (>2 and <18 months since diagnosis)
  • Willing to carry smartphone on their person for duration of study participation
  • Willing to wear smartwatch for duration of study participation

Exclusion criteria

  • Significant physical or mental disability that prevents completion of study activities
  • Lack of proficiency in English or Spanish

Trial design

Primary purpose

Supportive Care

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

25 participants in 1 patient group

Digital Phenotyping Arm
Experimental group
Description:
All participants (adolescents and young adults with cancer) will receive the digital phenotyping intervention, which includes wearing a smartwatch and using a smartphone-based EMA app over a 10-day period, with psychosocial assessments at baseline, day 10, and 2 months
Treatment:
Device: Device
Behavioral: Ecological Momentary Assessment (EMA) via My Personal Health Dashboard (MyPHD) Smartphone App

Trial contacts and locations

1

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Central trial contact

Olivia Borge

Data sourced from clinicaltrials.gov

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