80 Participants Needed

Visual Aid for Cancer Fatigue

(VAP Trial)

Recruiting at 2 trial locations
AP
ML
Overseen ByMegan Lattanze
Age: 18+
Sex: Any
Trial Phase: Academic
Sponsor: Wake Forest University Health Sciences
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial aims to understand the impact of cancer-related fatigue on survivors and to enhance discussions about it with healthcare providers. The goal is to develop a visual aid to facilitate conversations between patients and doctors about fatigue and to discover better management strategies. Cancer survivors who completed treatment over six months ago, have visited for long-term care, and experience significant fatigue may be suitable candidates for this trial.

As an unphased trial, this study offers participants the chance to contribute to meaningful improvements in patient-doctor communication and fatigue management strategies.

Will I have to stop taking my current medications?

The trial does not specify whether you need to stop taking your current medications. However, if you are on maintenance therapy or other cancer-related treatments, you would not be eligible to participate.

What prior data suggests that this visual aid is safe for use with cancer survivors and clinicians?

Research has shown that the CRF Visual Aid helps patients and healthcare providers communicate more effectively about cancer-related fatigue. As an educational resource, it poses no safety risks. It involves no medication or physical procedures, ensuring safety for participants. Patients can use this visual aid as part of their care without concern for side effects or negative reactions.12345

Why are researchers excited about this trial?

Researchers are excited about this trial because it aims to better understand cancer-related fatigue from the perspective of both survivors and clinicians. Unlike standard treatments that typically focus on medical interventions to manage fatigue, this study uses a mixed methods approach to gather detailed insights and personal experiences. By exploring how survivors and healthcare providers perceive and describe fatigue, the trial hopes to uncover new dimensions of the condition that are often overlooked, potentially leading to more personalized and effective management strategies. This approach could revolutionize how we address cancer-related fatigue, moving beyond one-size-fits-all solutions to more tailored care.

What evidence suggests that the CRF Visual Aid is effective for managing cancer-related fatigue?

Research shows that feeling very tired is a common and disruptive problem for people who have had cancer. Studies indicate that non-drug methods, such as talking therapy (CBT) and exercise, can help reduce this tiredness. Evidence suggests that healthcare providers manage this tiredness better when they properly check and assess it. This trial tests the CRF Visual Aid as a new tool to improve communication between patients and healthcare providers, potentially enhancing the use of these known methods. Early signs suggest that tools like visual aids could help people understand and manage their tiredness more effectively.678910

Who Is on the Research Team?

DB

Dori Beeler, PhD

Principal Investigator

Atrium Health Wake Forest Baptist Comprehensive Cancer Center

Are You a Good Fit for This Trial?

Inclusion Criteria

I can follow the study's requirements for its duration.
I can read, write, and speak English without needing an interpreter.
I identify as White, Black, African American, Hispanic, or Latino/a.
See 4 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Data Collection

Participants complete a six-minute walk test, surveys, and virtual video interviews

7 months
2-3 virtual interviews

Follow-up

Participants are monitored for qualitative themes and domain reflections

4 months

What Are the Treatments Tested in This Trial?

Interventions

  • CRF Visual Aid

How Is the Trial Designed?

2

Treatment groups

Experimental Treatment

Group I: SurvivorsExperimental Treatment1 Intervention
Group II: CliniciansExperimental Treatment1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Wake Forest University Health Sciences

Lead Sponsor

Trials
1,432
Recruited
2,506,000+

Atrium Health Levine Cancer Institute

Collaborator

Trials
30
Recruited
4,700+

Citations

Systematic Review and Meta-Analysis - PMC - PubMed Central

Existing evidence showed promising effects of 3 natural products in reducing CRF among cancer survivors.

Screening and Assessment of Cancer-Related Fatigue

Oncology care providers must be able to properly screen and/or assess CRF to provide effective intervention strategies throughout the cancer ...

Nonpharmacological interventions for cancer-related fatigue

CBT is effective in reducing CRF scores and improving the overall effectiveness of CRF treatment in cancer patients, as shown in three meta-analyses covering 31 ...

Cancer-Related Fatigue in Post-Treatment Cancer Survivors

Abstract. Background: Cancer-related fatigue (CrF) is the most common and disruptive symptom experienced by cancer survivors.

Cardio-Oncology Rehabilitation to Manage Cardiovascular ...

There is reasonable evidence to support the conclusion that exercise improves CRF after the completion of cancer therapy. For example, in a meta ...

IOWA DOT SAFETY ANALYSIS GUIDE

The visual presentation of crash data analysis can be generated in ICAT or in other programs including geographic information systems (GIS).

Everything You Need to Know About CRFs in Clinical Trials

A case report form (CRF) is a document designed to record all patient information that needs to be collected during a clinical trial.

CRASH REDUCTION FACTOR MANUAL

As new safety research data becomes available, the list will be evaluated to update, add, or remove some safety improvement countermeasures. ODOT is ...

Basics of case report form designing in clinical research - PMC

Designing a CRF is crucial in a clinical trial as it will aid in assessing the safety and efficacy of the medicinal product accurately. CRF should be designed ...

Hills | CRF Completion Guidelines

This chapter covers development, maintenance, and implementation of instructions for CRF completion, also called CRF Completion Guidelines (CCGs).