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NCT07710495Recruiting

Exercise to Improve Outcomes in Pancreatic Cancer

Exercise-Based Pre-, Peri- and Post-Surgery Intervention to Improve Clinical and Translational Outcomes in Patients Undergoing Whipple's Procedure: A Feasibility Study.

Source: ClinicalTrials.gov · Last updated 17 Jul 2026

Brief summary (registry, in English)

Pancreatic cancer surgery (Whipple's procedure) is a major operation that can lead to reduced physical fitness, delayed recovery, and difficulty starting chemotherapy after surgery. Exercise before and after surgery may help improve recovery, but it is not known whether a personalised exercise programme delivered throughout the surgical pathway is practical or acceptable for patients. The Exercise to Improve Outcomes in Pancreatic Cancer (ExO-PanC) study is a single-arm feasibility study that will recruit adults with suspected pancreatic ductal adenocarcinoma who are scheduled to undergo Whipple's procedure. Participants will receive an individualised exercise programme before surgery, during their hospital stay, and after discharge until the start of adjuvant chemotherapy. The programme will include aerobic exercise and resistance training prescribed according to each participant's fitness level. The primary objective is to determine whether this exercise programme is feasible by assessing recruitment, participant adherence, compliance with the prescribed exercise programme, and retention. Secondary exploratory objectives include evaluating surgical complications, initiation of adjuvant chemotherapy, physical fitness, quality of life, nutritional status, and blood, stool, and tumour biomarkers associated with clinical outcomes. Findings from this feasibility study will inform the design of a future multicentre randomised controlled trial evaluating the effectiveness of the ExO-PanC programme.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
60 (estimated)
First submitted
6 Jul 2026
Start date
6 Jul 2026
Primary completion date
1 Jun 2029
Lead sponsor
University of Surrey
NCT number
NCT07710495

What you commit to

  • Study type: Interventional
  • Planned participants: 60
  • From 6 Jul 2026 to the primary completion date, 1 Jun 2029
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Not scheduled for surgery

Other illness

  • A new diagnosis of Type 1 or Type 3c diabetes requiring management with insulin prescription will be excluded from the study.

Age

  • \<18 years age

Other

  • Cardiopulmonary exercise test (CPET) contraindications
  • Physical inability to perform CPET or undertake the program.
  • Lacking the capacity to consent
  • Unable to understand instructions in English

Who the study is looking for

  • Adults aged 18 years or older.
  • Planned to undergo upfront pancreatoduodenectomy (Whipple's procedure) for a suspected malignant periampullary mass.
  • Able and willing to provide written informed consent.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University of Surrey
Coordinator of this site? Confirm its status
GuildfordUnited KingdomRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.