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

Stanford University
NCT IDNCT07220343ClinicalTrials.gov data as of Apr 2026
Target enrollment

25

Study length

about 1.9 years

Ages

10–25

Locations

1 site in CA

What this study is about

Researchers are testing a device, called MyPHD, to help identify teens and young adults with cancer who need mental health support. The trial will use an app on smartphones to track how people are feeling throughout the day.

Simplified from trial records by PatientMatch.

What you may be asked to do

  • 1.Participate in Ecological Momentary Assessment (EMA) via My Personal Health Dashboard (MyPHD) Smartphone App
  • 2.Use Device

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
Standard

How treatment is administered

Treatment Assignment
All receive treatment

Everyone gets the investigational treatment.

Extracted study details

Pulled from the trial record to show what is being tested and what the study is measuring.

Endpoints

Primary: Change in Depressive Symptoms (Beck Depression Inventory - BDI)

Secondary: Change in Anxiety Symptoms (Beck Anxiety Inventory - BAI), Change in PTSD Symptoms (CROPS), Change in PTSD Symptoms (PCL-5), Change in Sleep Quality (Pittsburgh Sleep Quality Index - PSQI)

Body systems

Oncology