ClinicalTrials.Veeva

Menu

Building Empowerment and Coping Outcomes for CaNcer Patients, Survivors and Their Caregivers (BEACON)

C

Color Health

Status

Completed

Conditions

Caregiver Burnout
Survivorship
Cancer
Caregiving Stress

Treatments

Behavioral: Cancer Connect Program

Study type

Interventional

Funder types

Industry

Identifiers

NCT06353178
20240314

Details and patient eligibility

About

Cancer has a psychological, emotional and social impact beyond a patient's physical health. This study examines three new online peer mental-wellness support program for cancer patients, survivors or their caregivers. Each program teaches evidence-based skills, in the context of that groups lived experience, to manage the emotional impact of cancer. This study examines the impact of that program.

Full description

Cancer has a psychological, emotional and social impact beyond a patient's physical health. These problems often ripple beyond the individual with the diagnosis, to their broader community, and also beyond a cancer treatment course into survivorship. As a result, there are a wide range of socioemotional needs in those who have been impacted by cancer. Further, these emotional impacts have a direct impact on morbidity and mortality of cancer. A new peer mental-wellness support program, called Color Cancer Connect (CCC) supports cancer patients, survivors and their caregivers by teaching them evidence-based skills to manage the emotional impact of cancer. This study will examine all three programs (i.e., patient, survivor, caregiver) to gather data to measure the impact of the program on emotional well-being, quality of life and health behaviors.

Enrollment

133 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Lived experience as either a current cancer patient, cancer survivor or caregiver of someone with cancer
  • Adult - 18+
  • Has health insurance provided by employer or union (can be dependent of person on insurance)
  • Read/speak English
  • Have access to internet and personal email account

Exclusion criteria

  • Severe mental illness that is disruptive to other group members

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

133 participants in 2 patient groups, including a placebo group

Cancer Connect Program
Experimental group
Description:
Participants assigned to this arm will be able to attend the online peer program upon entering the study.
Treatment:
Behavioral: Cancer Connect Program
Waitlist
Placebo Comparator group
Description:
Participants assigned to this arm will be on a waitlist and will be invited to join the online peer program in 3 months.
Treatment:
Behavioral: Cancer Connect Program

Trial contacts and locations

1

Loading...

Central trial contact

Cecilia M Votta, PhD; Cynthia Neben, PhD

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems