Actively Recruiting
Patient Descriptors Of Cancer-Related Fatigue: A Mixed Methods Pilot Study Of Cancer Survivors
Led by Wake Forest University Health Sciences · Updated on 2026-02-02
80
Participants Needed
3
Research Sites
168 weeks
Total Duration
On this page
Sponsors
W
Wake Forest University Health Sciences
Lead Sponsor
A
Atrium Health Levine Cancer Institute
Collaborating Sponsor
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Patient Descriptors Of Cancer-Related Fatigue: A Mixed Methods Pilot Study Of Cancer Survivors
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Ability to comply with study procedures for the duration of the study
- Written informed consent and HIPAA authorization for release of personal information
- Ability to read, write, understand, and converse in English without an interpreter
- Men and women aged 18 years or older at the time of consent
- White or Caucasian, Black or African American, or Hispanic or Latino/a
- History of at least one visit for long-term care monitoring post curative treatment at LCH and/or Charlotte or Winston-Salem campuses of AHWFBCCC
- Completed curative cancer treatment more than 6 months ago with no detectable cancer
- Self-reported fatigue score of 4 or higher on the Numerical Rating Scale
- Clinicians currently seeing oncology patients for survivorship care at LCH and/or Charlotte or Winston-Salem campuses of AHWFBCCC
You will not qualify if you...
- Continuing maintenance therapy or other cancer-related treatments such as immunotherapy or hormonal therapy
- History of or current severe or untreated depression
- Hemoglobin less than 11 g/dL at last CBC SOC lab test
- History or diagnosis of dementia
- Conditions that may interfere with study participation or assessment results, including medical comorbidities or brain tumors/metastases
- No access to internet or Wi-Fi
- No exclusion criteria listed for clinicians
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 3 locations
1
Levine Childrens Hospital Pediatric Cancer and Blood Disorders
Charlotte, North Carolina, United States, 28203
Actively Recruiting
2
Levine Cancer Institute
Charlotte, North Carolina, United States, 28204
Actively Recruiting
3
Wake Forest Baptist Comprehensive Cancer Center
Winston-Salem, North Carolina, United States, 27157
Actively Recruiting
Research Team
M
Megan Lattanze
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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