What this study is
The purpose of this research study is to better understand how cancer-related fatigue affects patients and how it's discussed with providers. This information will be used to develop an educational resource (visual aid poster) that could help individuals and their providers talk about cancer-related fatigue and which may help individuals better manage this symptom.
What's being tested
- CRF Visual Aid
Intervention · BEHAVIORAL
After all qualitative interviews and associated quantitative data analysis are complete, the visual aid will be created to illustrate, through a type of Venn Diagram, how the data are related.
Study details
- Sponsor
- Wake Forest University Health Sciences
- Conditions
- Cancer · Fatigue
- Enrolling
- 80 people
- Starts
- 2025-03-12
- Est. completion
- 2028-06
- Record
- View on ClinicalTrials.gov ↗
Who can join
Age 18 Years and overSex ALLHealthy volunteers Not acceptedYou may qualify if
- Ability to comply with study procedures for the duration of the study Survivors:; Written informed consent and HIPAA authorization for release of personal information; Ability to read/write, understand and converse in English without the need for an interpreter; Men and women aged ≥ 18 years at the time of consent; White or Caucasian, Black or African American, or Hispanic or Latino/a; History of at least one visit for the purpose of monitoring long term care post curative treatment at LCH and/or the Charlotte or Winston-Salem campuses of AHWFBCCC; Completed curative treatment > 6 months ago for any cancer type, with no detectable evidence of cancer; Self-reported fatigue score of ≥ 4 on the Numerical Rating Scale Clinicians:; Currently see oncology patients (any cancer type) for survivorship care at LCH and/or the Charlotte or Winston-Salem campuses of AHWFBCCC
You can't join if
- Survivors:
- Continuing maintenance therapy or other cancer-related treatment (i.e. immunotherapy or hormonal therapy)
- History of or current severe or untreated depression
- Hemoglobin <11g/dL at last CBC SOC lab collection
- History/diagnosis of dementia
- Factors or conditions, for which participation may (1) not be in the best interest or (2) interfere with study assessment results (e.g. medical comorbidities, primary brain tumor/metastases)
- No access to internet/Wi-Fi Clinicians:; None
Sign in and we'll check these against your records.Full criteria on ClinicalTrials.gov ↗
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Study locations (3)
3 openContact for 2 of 3 open sites
- Megan Lattanze · Contact(980) 442-4239Megan.Lattanze@advocatehealth.org
- Dori Beeler, PhD · Principal investigator
Levine Childrens Hospital Pediatric Cancer and Blood Disorders
Charlotte, North Carolina, United States
RecruitingLevine Cancer Institute
Charlotte, North Carolina, United States
RecruitingWake Forest Baptist Comprehensive Cancer Center
Winston-Salem, North Carolina, United States
- Sarah Birken, PhD · Contact336-713-3558sbirken@wakehealth.edu
- Sarah Birken, PhD · Principal investigator
Recruiting
Study team
Sponsor
Wake Forest University Health Sciences
Study ID IRB00119101
Principal investigator
Dori Beeler, PhD
Atrium Health Wake Forest Baptist Comprehensive Cancer Center
Frequently asked questions
The sponsor hasn't published answers to common questions for this trial.