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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05227599
Other study ID # IRB-55183
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 1, 2021
Est. completion date March 24, 2022

Study information

Verified date September 2023
Source Stanford University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine the feasibility and acceptability of tracking survivors' and their caregivers, stressors, affect, and symptoms using an electronic diary method, in the time period surrounding their routine check- up with their oncologist.


Recruitment information / eligibility

Status Completed
Enrollment 56
Est. completion date March 24, 2022
Est. primary completion date March 24, 2022
Accepts healthy volunteers No
Gender All
Age group 11 Years to 25 Years
Eligibility Inclusion Criteria: 1. 11-25 years old 2. previously received a pediatric cancer diagnosis and treatment for such 3. completed cancer treatment <5 years ago, in remission 4. Own a smart phone or tablet 5. are English proficient Exclusion Criteria: - no cognitive, motor, or sensory deficits that could preclude completion of study measures.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Online survey questionnaire
Participants will complete a brief online survey every morning and evening within 1 hour of waking and 1 hour of going to sleep. The surveys will be a combination of measures used to assess affect, stress, and symptoms

Locations

Country Name City State
United States Stanford University San Francisco California

Sponsors (1)

Lead Sponsor Collaborator
Stanford University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Online survey questionnaire participants will complete a brief online survey every morning and evening within 1 hour of waking and 1 hour of going to sleep 21 days
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