Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT07478185

Prehab for Pancreatic Cancer Surgery

Led by University of Massachusetts, Worcester · Updated on 2026-04-03

20

Participants Needed

1

Research Sites

139 weeks

Total Duration

On this page

Sponsors

U

University of Massachusetts, Worcester

Lead Sponsor

P

Pancreatic Cancer Alliance

Collaborating Sponsor

AI-Summary

What this Trial Is About

The goal of this clinical study is to test whether a structured prehabilitation program can be successfully used by adults with pancreatic cancer who are receiving chemotherapy before planned surgery. Prehabilitation is a program designed to improve a person's physical fitness, nutrition, and symptom control before surgery. The study's main hypothesis is that patients with pancreatic cancer can take part in and adhere to a multimodal prehabilitation program during chemotherapy, and that doing so may improve physical function, patient experience, and early recovery after surgery.

CONDITIONS

Official Title

Prehab for Pancreatic Cancer Surgery

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 6 18 years
  • Diagnosis of pancreatic ductal adenocarcinoma (PDAC)
  • Planned neoadjuvant chemotherapy prior to planned surgical resection
  • Medically stable and cleared to participate in physical activity/exercise programming
  • Able to provide informed consent
  • Ability to read, write and understand English
Not Eligible

You will not qualify if you...

  • Age <18 years
  • Pregnant
  • Prisoner
  • Severe cognitive impairment that precludes informed consent or participation
  • Contraindications to physical activity, including unstable cardiac disease, severe pulmonary disease, or recent myocardial infarction

AI-Screening

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Trial Site Locations

Total: 1 location

1

UMass Memorial Medical Center

Worester, Massachusetts, United States, 01655

Actively Recruiting

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Research Team

K

Kayla R Widdowson, MD

CONTACT

J

James M Lindberg, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

1

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