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Clinical Trial NCI 12Q06

Title
Targeted eHealth Intervention to Reduce Fear of Recurrence (FoR) Among Cancer Survivors: FoRtitude
Principal Investigator
Lynne Wagner
Details
  • Status: Accepting New Patients
  • Study Type: Supportive Care, QOL
  • Protocol No:.NCI 12Q06
Purpose
The purpose of this study is to create a web-based application titled FoRtitude that teaches breast cancer survivors how to reduce their fear of cancer recurrence.
Overview
If you agree to participate, you will be asked to complete questionnaires online about your moods and emotions when you enroll in the study. You will complete the same questionnaires again one and two months later.
Eligibility
Some of the eligibility criteria include:
  • Be a female aged 19 or older
  • Have had breast cancer (stage I-III)
  • Have completed treatment for breast cancer (current hormonal treatment allowed)
  • Own a mobile phone and use it to send and receive text messages
  • Have an e-mail account and have access to the internet
Note: This is only a partial list of eligibility criteria. Please contact the Lurie Cancer Center for complete screening information if you are interested in this clinical trial.
Description of Treatment
FoRtitude is a web-based application designed to teach breast cancer survivors ways of managing fear of cancer recurrence. Participants will be asked to use FoRtitude daily and asked to log-in no less than 4 times per week for a period of 4 weeks, twice to review educational material and two additional times to use online tools which help apply the educational material. The educational material will be primarily text, video and audio. Each lesson will take 10-15 minutes to complete. Interactive tools will support learning and development of skills to improve the ability to cope. Interactive tools will take 5-10 minutes and participants will be encouraged to use tools daily. Participants may be contacted weekly by a telephone coach for calls lasting about 15 minutes to ask about FoRtitude. The FoRtitude site will continue to be available to participants for a total of 8 weeks. Participants’ name and identity will be kept confidential. For the first phase of the study, the research team will use comments and input from participants to make sure FoRtitude is helpful and easy for cancer survivors to use. For the second phase, the research team will use questionnaire responses to evaluate whether FoRtitude was effective at reducing fears about recurrence.
Contact
Sara Duffey
Clinical Research and Education Specialist
Robert H. Lurie Comprehensive Cancer Center
312.695.1102
cancertrials@northwestern.edu

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last updated: 27-Nov-14 08:14 AM

 

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