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Recruiting NCT05641961

Mobile App to Help Survivors of Childhood Cancer Navigate Long-Term Follow-Up Care

No phase Interventional Childhood Cancer Hematopoietic and Lymphoid Cell Neoplasm Malignant Solid Neoplasm

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Survivorship mobile application, Questionnaires.
Who it may be relevant to
Registry conditions: Childhood Cancer, Hematopoietic and Lymphoid Cell Neoplasm, Malignant Solid Neoplasm. Basic parameters: No limits · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Utilizing a Mobile App to Help Survivors of Childhood Cancer Navigate Long-Term Follow-Up Care

Overview

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.

Detailed description

PRIMARY OBJECTIVE:

I. To determine the difference in survivor/caregiver knowledge and understanding of diagnosis, treatment information, and follow-up needs using the survivorship app.

SECONDARY OBJECTIVE:

I. To validate the usability and effectiveness of the survivorship mobile application.

OUTLINE:

Participants are seen in the survivorship clinic and receive education about potential late effects and the survivorship application on study. Participants then use the survivorship app for 4 months on study.

Interventions

  • Behavioral Survivorship mobile application
    Mobile phone application
  • Other Questionnaires
    Questionnaires assessing cancer knowledge and system usability will be delivered to participants via Survivorship App

Primary outcome measures

  • Change in knowledge questionnaire score [Time frame: Up to 4 months]
Secondary outcome measures (1)
  • System usability scale (SUS) score > 68 [Time frame: Up to 2 months]

Eligibility criteria

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.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
N/A
Model
Single group
Masking
Open label
Primary purpose
Health services research

Study locations

United States · 1 center
  • University of California, San Francisco — San Francisco

Identifiers

NCT: NCT05641961 · 220813 · NCI-2022-09452

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗