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Not yet recruiting NCT07122492

A Targeted Electronic Health Approach to Reduce Fear of Recurrence in Breast Cancer Survivors (FoRtitude)

No phase Interventional Breast Cancer Survivor Fear of Cancer Recurrence

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: FoRtitude 2.0, Attention Control.
Who it may be relevant to
Registry conditions: Breast Cancer Survivor, Fear of Cancer Recurrence. Basic parameters: from 18 years · Female.
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 →

Unsure about the terms? Read our patient guide →

Official title

Randomized Controlled Trial of FoRtitude: Targeted eHealth Intervention to Reduce Fear of Recurrence Among Breast Cancer Survivors in Community Oncology Settings

Overview

The goal of this study is to determine if the intervention or if general information about being a breast cancer survivor can help Breast Cancer Survivors reduce their fear of recurrence. The main question it aims to answer are: Can the FoRtitude intervention lower the fear of recurrence for Breast Cancer Survivors? Participants will: Answer questions about their fear of recurrence. Be randomized to 1 of the 3 following options: (1) a weblink to access an eHealth intervention which includes a website and an optional interactive text-messaging feature, (2) a weblink to a non-interactive website that will include links to external websites with general information that may be helpful for Breast Cancer Survivors, or (3) you will need to talk with your oncology team about your concerns about recurrence or seek psychosocial care in the community. Be asked to fill out questionnaires 5 times for up to 18 months.

Interventions

  • Behavioral FoRtitude 2.0
    A website and an interactive text-messaging feature
  • Behavioral Attention Control
    Access to the non-interactive study intervention website that lists links to help you access websites that provide information to read and resources for breast cancer survivors.

Primary outcome measures

  • Fear of Cancer Recurrence Inventory (FCRI) [Time frame: From 1 month post-intervention to 3 months post-intervention]
Secondary outcome measures (2)
  • Difference in fear of recurrence based on race across all arms [Time frame: From enrollment to 3 months]
  • Change in quality of life measures [Time frame: At all time points, including long term outcomes at 6, 12 and 18 months.]

Eligibility criteria

Inclusion criteria

  • Participant must be ≥ 18 years of age.
  • Participant must have had histologically confirmed Stage 0-III breast cancer at time of diagnosis.
  • Participant must have completed primary treatment 1-10 years prior to Step 0 registration.

NOTE: Current hormonal therapy is allowed. NOTE: Primary treatment can include chemotherapy and/or surgery and/or radiation therapy.

\- Participant must be receiving their care (cancer treatment or survivorship care) from an oncology provider affiliated with the NCORP site and are expected to continue care at the site for the next 18 months.

NOTE: This eligibility criteria is intended to ensure access to healthcare utilization data. Oncology provider can include an Advance Practice Provider, Advance Nurse Practitioner, oncologist, primary care provider, or nurse or physician responsible for survivorship care.

  • Participant must have no evidence of active cancer of any type at the time of Step 0 registration (per the assessment of the physician), excluding local basal cell or squamous cell carcinoma.
  • Participant must be fluent in written and spoken English.
  • Participant must have an ECOG Performance Status of 0-2.
  • Participant must have the ability to understand and the willingness to sign a written informed consent document. Participants with impaired decision-making capacity (IDMC) are not eligible.
  • Participant must complete the FCRI 9-item severity scale and report a score of 13 or higher.
  • Participant must have access to the internet (via smartphone, tablet, or computer).

NOTE: The restriction to those with internet access is based on the primary intention of the study which involves internet-based delivery intervention content delivered via the internet.

  • Participant must have completed the Baseline Assessment within 60 days of Step 0 registration.
  • Randomization to Step 1 must occur within 60 days of Step 0 registration.

Exclusion criteria

  • Participant must not have any psychiatric or cognitive conditions that may affect the participant's ability to accurately provide self-report data, per clinical discretion.

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

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Other

Study locations

United States · 1 center
  • UNC Chapel Hill School of Medicine Public Health — Chapel Hill

Identifiers

NCT: NCT07122492 · EAQ181

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗