A Web-Based Dyadic Intervention to Manage Psychoneurological Symptoms for Patients With Colorectal Cancer and Their Caregivers

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

This clinical trial studies how well a web-based dyadic intervention works to manage psychoneurological symptoms for patients with colorectal cancer and their caregivers. Patients with colorectal cancer receiving chemotherapy experience severe and distressing psychoneurological symptoms that include fatigue, depression, sleep disturbance, pain, and cognitive dysfunction. When these co-occurring symptoms are undertreated, they negatively affect functional status, survival rates, and quality of life of patients as well as decrease health outcomes of their family caregiver. A critical need exists to develop an effective and novel intervention that focuses on patients with colorectal cancer receiving chemotherapy and their caregivers. A web-based dyadic intervention holds great promise to reduce psychoneurological symptoms burden and improve quality of life for patients with colorectal cancer receiving chemotherapy and advance intervention development and implementation in cancer supportive care and health equity.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: t
View:

⁃ Patients:

• Age \>= 18 years

• Diagnosed with colorectal cancer

• Life expectancy \> 12 months

• Receiving active chemotherapy

• Self-reported at least two psychoneurological symptoms (based on the symptom measures' cutoff scores)

• Identified primary caregiver (i.e., family members or significant others identified by the patients as their primary source of emotional and physical support)

• Access to the Internet

• Fluent in English

⁃ Caregivers:

• Age \>= 18 years

• Primary caregiver

• Access to the Internet

• Fluent in English

Locations
United States
Georgia
Emory University/Winship Cancer Institute
RECRUITING
Atlanta
Contact Information
Primary
Yufen Lin, PhD, RN
yufen.lin@emory.edu
404-712-9823
Backup
Canhua Xiao, PhD, RN
canhua.xiao@emory.edu
404-712-9823
Time Frame
Start Date: 2023-05-01
Estimated Completion Date: 2026-10-01
Participants
Target number of participants: 56
Treatments
Experimental: Supportive care (CRCWeb intervention)
Patients and caregivers attend a CRCweb intervention over 8 weeks. Patients and caregivers complete interviews and surveys throughout the trial.
Sponsors
Collaborators: Oncology Nursing Society
Leads: Emory University

This content was sourced from clinicaltrials.gov