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

N/ARecruitingNCT07220343

Stanford University25 enrolled

Overview

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.

Study Type

INTERVENTIONAL

Allocation

Purpose

SUPPORTIVE_CARE

Masking

NONE

Enrollment

Conditions

Cancer Adolescents

Interventions

DeviceDEVICE

Participants will wear a wrist-based wearable device for 10 days to passively track physiological data (heart rate, steps, sleep, etc.).

Ecological Momentary Assessment (EMA) via My Personal Health Dashboard (MyPHD) Smartphone AppBEHAVIORAL

Participants will respond to ecological momentary assessments (EMA) via smartphone to actively report on sleep, mood, stress, and eating habits across a 10-day period.

Eligibility

Sex: ALLMin age: 10 YearsMax age: 25 Years

Medical Language ↔ Plain English

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

Locations (1)

Stanford University

Palo Alto, California, United States

RECRUITING

Outcomes

Primary Outcomes

Change in Depressive Symptoms (Beck Depression Inventory - BDI)

The Beck Depression Inventory-II (BDI-II; range 0-63) will be used to measure changes in depressive symptoms among adolescents and young adults over time. Higher scores indicate greater depressive symptom severity.

Time frame: Baseline, Day 10, 2 months

Secondary Outcomes

Participant Retention Rate (MyPHD App and Wearable Device)

Percentage of participants who remain active in the study through the 2-month follow-up period using the MyPHD app and wearable device.

Time frame: Baseline to 2 months

Adherence to EMA Prompts

Mean percentage of EMA prompts completed by participants using the MyPHD mobile app during the 2-month study period. Completion will be assessed via EMA system analytics.

Time frame: Baseline to 2 months

Wearable Device Return and Use Rate

Percentage of participants who return and use the wearable device as instructed during the study period. Device use will be tracked through backend device usage logs.

Time frame: Baseline to 2 months

Change in Anxiety Symptoms (Beck Anxiety Inventory - BAI)

Measures changes in self-reported anxiety symptoms across the study period.

Time frame: Baseline, Day 10, 2 months

Change in PTSD Symptoms (CROPS)

PTSD symptoms are measured using the Child Report of Post-traumatic Symptoms (CROPS) for child participants.

Time frame: Baseline

Change in PTSD Symptoms (PCL-5)

Central Contacts

Olivia Borge

CONTACT

(650) 723-9392 oborge@stanford.edu

Data from ClinicalTrials.gov

This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.