Recruiting

Survivorship App

Sponsor:

UCLA

Code:

NCT05641961

Conditions

Childhood Cancer

Hematopoietic and Lymphoid Cell Neoplasm

Malignant Solid Neoplasm

Eligibility Criteria

Sex: All

Age: 0+

Healthy Volunteers: Accepted

Interventions

Survivorship mobile application

Questionnaires

Study Details

Brief summary:

This clinical trial studies the effectiveness of a newly developed survivorship mobile application (app) designed for survivors, or their caregivers, of childhood cancer to help them better navigate long-term follow-up care. The survivorship app provides survivors access to their treatment history and follow-up recommendations, improves knowledge of their diagnosis, treatment, risks, and recommended follow-up care by using a message notification. The ability to quickly connect and establish care planning may enhance adherence to recommended follow-up.

Conditions

Childhood Cancer

Hematopoietic and Lymphoid Cell Neoplasm

Malignant Solid Neoplasm

Study ID

NCT05641961

Start date

Nov 29, 2022

Status verified date

Jul, 2025

Completion date

Apr 30, 2026

Anticipated

Primary completion date

Apr 30, 2026

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 0+

Healthy Volunteers: Accepted

Inclusion Criteria:

  • Survivors of childhood cancer attending Survivorship Clinic at University of California, San Francisco (UCSF) OR caregivers of a childhood cancer survivor attending Survivorship Clinic at UCSF.
  • Must have a mobile device (smartphone or smart-tablet) with service plan.
  • Must have ability to read, write, and understand English language.

Exclusion Criteria:

  • An individual who does not meet any of the criteria mentioned above will be excluded from participation in this study.

Study Design

Enrollment

30 participants

Anticipated

Intervention Model

Single group

Primary purpose

Health Services Research

Interventions and Outcome Measures

Arms

experimental: Survivorship Mobile Application

Participants are seen in the survivorship clinic and receive education about potential late effects and the survivorship application on study. Participants enrolled in this study will be asked to complete two self-administered questionnaires at 4 time points. Questionnaires will be designed and made available electronically, to be completed on the participant's personal mobile device (e.g., mobile phone).

Interventions

Survivorship mobile application

Mobile phone application

Questionnaires

Questionnaires assessing cancer knowledge and system usability will be delivered to participants via Survivorship App

Primary outcome measure

  • Change in knowledge questionnaire score [ Time Frame: Up to 4 months ]

Central Contacts and Locations

Central contacts

Patricia Murphy, RN

(415) 476-2700Patricia.Murphy@ucsf.edu

Locations

University of California, San Francisco

Recruiting

San Francisco, California, United States, 94143

Contacts

Patricia Murphy, RN

415-476-2700Patricia.Murphy@ucsf.edu

Principal Investigator:

Robert Goldsby, MD

More Information

Sponsor

University of California, San Francisco

Last update posted

Jul 23, 2025

Last verified

Jul, 2025

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-08. This information was provided to ClinicalTrials.gov by University of California, San Francisco on 2025-07-23.