Actively Recruiting
Testing the Feasibility of Psychosocial Oncology Support During Neoadjuvant Therapy for Patients With Localized Pancreatic Cancer
Led by Ohio State University Comprehensive Cancer Center · Updated on 2026-02-19
60
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are evaluating a psychosocial oncology intervention designed to support patients with localized pancreatic cancer undergoing neoadjuvant therapy before surgery. Neoadjuvant therapy, which may include chemotherapy and/or radiation, aims to shrink the tumor and reduce cancer spread, improving surgery success and survival rates. Despite these benefits, this treatment can cause significant physical and emotional side effects, so adding psychosocial support may help improve patients' quality of life during this phase. The study involves patients receiving weekly telehealth sessions with a psychologist for 40 minutes over four weeks, alongside their usual physical therapy and nutritional therapy referrals. This psychosocial care is provided during the neoadjuvant therapy period, with the goal to ease emotional distress and enhance overall well-being. The intervention is tested for feasibility and acceptability, with patients continuing their standard medical treatments throughout. Participants will be monitored for up to one year to assess how well the psychosocial intervention is accepted and its effects on quality of life, mood, worry, and feelings of uncertainty. Researchers will collect data through questionnaires and interviews to evaluate these outcomes. Safety and overall health will also be followed, ensuring comprehensive support while patients prepare for surgery and recovery.
CONDITIONS
Brief Title
A Brief Psychological Intervention to Improve Emotional Well-Being During Neoadjuvant Therapy for Pancreatic Cancer
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adults 18 years of age or older
- Newly diagnosed with localized pancreatic ductal adenocarcinoma
- Planning to start neoadjuvant therapy before surgical removal of the tumor
- Neoadjuvant therapy and/or surgery may occur at different medical facilities
You will not qualify if you...
- Prisoners
- Unable to provide consent
- Unlikely to have surgery after neoadjuvant therapy due to anatomy or health status
- Confirmed or suspected metastatic (spread) disease
- Already received two or more cycles of chemotherapy
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - 4 weeks
Participants meet with a psychologist via telehealth for weekly 40-minute psychosocial oncology sessions and attend standard physical therapy and nutritional therapy appointments during neoadjuvant therapy.
Weekly visits via telehealth and additional physical and nutritional therapy appointments
Trial Site Locations
Total: 1 location
1
Ohio State University Comprehensive Cancer Center
Columbus, Ohio, United States, 43210
Actively Recruiting
Research Team
T
The Ohio State University Comprehensive Cancer Center
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
HEALTH_SERVICES_RESEARCH
Number of Arms
1
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