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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT03363711
Other study ID # UPCC 26916
Secondary ID
Status Active, not recruiting
Phase
First received
Last updated
Start date March 1, 2017
Est. completion date December 1, 2024

Study information

Verified date January 2024
Source Abramson Cancer Center at Penn Medicine
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The proposed project will leverage two programs of research at UPenn and CHOP that are delivering technology-based interventions to adolescent and young adult (AYA) cancer survivors. In the proposed study, all AYA survivors will receive a care plan via a tool (Smart-ALACC). They will then be randomized to receive (or not) a mobile health application (AYA STEPS) that will provide tailored messages to enhance uptake of their care plan.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 25
Est. completion date December 1, 2024
Est. primary completion date December 1, 2019
Accepts healthy volunteers No
Gender All
Age group 15 Years to 29 Years
Eligibility Inclusion Criteria: - AYA is 15-29 year old with a history of a malignant cancer diagnosis; - Completed cancer treatment and are currently in remission or receiving cancer survivorship care; - Seen for follow-up oncology care at CHOP or Penn; - For AYA less than 18 years old, must have a caregiver to provide informed consent. Exclusion Criteria: - Cognitive impairments that would limit AYA ability to independently care for health as determined by the medical team. - Absence of the inclusion criteria

Study Design


Related Conditions & MeSH terms

  • Adolescent and Young Adult (AYA) Cancer Survivors

Intervention

Other:
AYA STEPS
a mobile health application

Locations

Country Name City State
United States Abramson Cancer Center of the University of Pennsylvania Philadelphia Pennsylvania

Sponsors (1)

Lead Sponsor Collaborator
Abramson Cancer Center at Penn Medicine

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of Completed mobile data and questionnaires 10 years
See also
  Status Clinical Trial Phase
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