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Empowering Cancer Survivors Through Information Technology

Not Applicable
Completed
Conditions
Cancer Survivor
Interventions
Behavioral: UMFollowUp
Other: Standard of Care
Registration Number
NCT01593618
Lead Sponsor
Masonic Cancer Center, University of Minnesota
Brief Summary

This is a randomized controlled trial of a web-based informational intervention (UMFollowUp) for adolescent and young adult survivors of childhood cancer to improve cancer knowledge and psychosocial functioning.

Detailed Description

Individuals randomly assigned to the control group will receive standard of care for the duration of their participation. This means they will continue to receive information regarding their diagnosis, treatments and ongoing health needs from their provider (no access to website).

Individuals randomly assigned to the treatment group will receive access to UMFollowUp, a secure, HIPAA-compliant website.

All participants will be asked to complete paper-and-pencil surveys at baseline and 9 months later to determine the impact of the web-based intervention.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
53
Inclusion Criteria
  • History of diagnosis of hematologic malignancy or malignant neoplasm, and in disease free remission at time of recruitment.
  • Must be English-speaking and have access to a computer with internet access, and must have completed treatment at University of Minnesota Medical Center-Fairview for cancer.
Exclusion Criteria
  • Individual with significant visual impairments and neurologic/cognitive difficulties which limit their ability to see and under our outcome questionnaires or website content will be excluded from participation.

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Web-Based InterventionUMFollowUpUMFollowUp - web-based internet resource for information about their diagnostic histories, recommendations for follow-up care, and tips to enhance their treatment, psychosocial and physical well-being.
Standard of CareStandard of CarePatients will receive information regarding their diagnosis, treatments, and ongoing health needs from their provider, but will not be provided access to the website.
Primary Outcome Measures
NameTimeMethod
Cancer Knowledge SurveyTime of Enrollment and 9 Months Later

Measure of patient reported knowledge of their cancer diagnosis, history and treatments.

Secondary Outcome Measures
NameTimeMethod
State Trait Anxiety InventoryTime of Enrollment and 9 Months Later

A measure of self-reported anxiety.

Cancer Rehabilitation Evaluation SystemTime of Enrollment and 9 Months Later

Short Form (SF) Medical Interaction Subscale

Herth Hope IndexTime of Enrollment and 9 Months Later

A measure of self-reported hope.

SF-36 QuestionnaireTime of Enrollment and 9 Months Later

A measure of quality of life.

Multidimensional Scale of Perceived Social SupportTime of Enrollment and 9 Months Later

A measure of self-reported social support.

Health Locus of Control ScaleTime of Enrollment and 9 Months Later

A measure of self-reported locus of control.

Trial Locations

Locations (1)

Masonic Cancer Center, University of Minnesota

🇺🇸

Minneapolis, Minnesota, United States

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