Clinical trial Recruiting at 1 site Interventional Ages 18 and up

Brief telehealth psychological support during pre-surgery (neoadjuvant) treatment for localized pancreatic cancer

Official title: Testing the Feasibility of Incorporating Psychosocial Oncology During Neoadjuvant Therapy for Patients With Pancreatic Cancer

Run by Ohio State University Comprehensive Cancer Center · NCT07124611 · Data updated 2026-11-12

We will try weekly 40-minute telehealth sessions with a psychologist to reduce stress and improve quality of life for people with localized pancreatic cancer receiving neoadjuvant chemotherapy or radiation.

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment60 (estimated)
SponsorOhio State University Comprehensive Cancer Center
Academic / other
Drugs / interventionschemotherapy, radiation
Locations1 site (Columbus, Ohio)
StatusRecruiting
StartedDecember 22, 2025
Main results expectedDecember 31, 2026
Study endsDecember 31, 2026
Registry record updatedFebruary 19, 2026
Trial IDNCT07124611 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults (≥18) newly diagnosed with localized pancreatic ductal adenocarcinoma who plan to start neoadjuvant chemotherapy and/or radiation and present to the Ohio State University Comprehensive Cancer Center.

Probably not a fit

Patients with confirmed or presumed metastatic disease, those unlikely to undergo surgical resection after neoadjuvant therapy, people who have already received two or more chemotherapy cycles, prisoners, or those unable to consent are not eligible and unlikely to benefit from this intervention.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This single-center intervention enrolls adults with newly diagnosed localized pancreatic ductal adenocarcinoma who plan to start neoadjuvant therapy. Participants receive one 40-minute telehealth session per week with a psychologist for four weeks, alongside standard referrals for nutritional and physical therapy. The study will measure feasibility and acceptability and collect preliminary data on quality of life and stress/anxiety outcomes. Patients with metastatic disease, those unlikely to undergo surgery, or who have already received two or more chemotherapy cycles are excluded.

Why it matters

Potential benefit: If successful, the intervention could reduce anxiety and improve quality of life during pre-surgery treatment, helping patients better tolerate therapy and prepare for surgery.

How similar studies have gone: Related psychosocial and prehabilitation programs in other cancer populations have shown reductions in distress and improvements in quality of life, but few studies have tested brief telehealth psychological interventions specifically during neoadjuvant therapy for pancreatic cancer.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Adults ≥ 18 years of age
* Patient:

  * Newly diagnosed patients with localized pancreatic ductal adenocarcinoma (PDAC) presenting to Ohio State University Wexner Medical Center-Comprehensive Cancer Center (OSUMC-CCC)
  * Plans to initiate neoadjuvant therapy prior to surgical resection
  * Neoadjuvant therapy (NT) and/or surgery may occur at another facility

Exclusion Criteria:

* Prisoners
* Persons unable to provide consent
* Patients unlikely to undergo surgical resection following NT based on anatomical or performance status considerations
* Confirmed or presumed metastatic disease
* Already received ≥ 2 cycles of chemotherapy

Where it's running

  • Ohio State University Comprehensive Cancer Center
    Columbus, Ohio, United States
    Recruiting

Study contacts

  • Principal investigator: Jordan M Cloyd, MD — Ohio State University Comprehensive Cancer Center
  • Study coordinator: The Ohio State University Comprehensive Cancer Center
  • Email: OSUCCCClinicaltrials@osumc.edu
  • Phone: 800-293-5066

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.