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Exercise to Improve Outcomes in Pancreatic Cancer (ExO-PanC)

2026年7月13日 更新者:University of Surrey

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

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.

研究概览

详细说明

Pancreatic ductal adenocarcinoma (PDAC) is associated with poor survival, reduced physical function, and a high burden of treatment-related morbidity. Patients undergoing pancreaticoduodenectomy (Whipple's procedure) often experience substantial declines in cardiorespiratory fitness and muscle function before and after surgery, which may contribute to postoperative complications, delayed recovery, and reduced likelihood of receiving adjuvant chemotherapy. While prehabilitation programmes are increasingly incorporated into routine care, current approaches are not typically individualised using objective measures of physical fitness and generally do not extend across the entire perioperative pathway.

The Exercise to Improve Outcomes in Pancreatic Cancer (ExO-PanC) study has been developed to evaluate the feasibility of a personalised exercise programme delivered before surgery, during hospital admission, and throughout postoperative recovery until the commencement of adjuvant chemotherapy. Exercise prescriptions will be individualised using cardiopulmonary exercise testing (CPET), muscle strength assessments, and functional performance measures, allowing exercise intensity and progression to be tailored to each participant's physiological capacity.

Participants will undergo repeated assessments of cardiorespiratory fitness, physical function, muscle strength, nutritional status, quality of life, and biological sampling throughout the study. Blood, stool, and surgically resected tumour tissue will be collected to explore biomarkers associated with clinical outcomes and responses to exercise.

The primary objective of this feasibility study is to determine whether the ExO-PanC intervention can be successfully delivered across the perioperative pathway by evaluating participant recruitment, adherence, compliance with prescribed exercise, and study retention. Exploratory analyses will investigate surgical complications, initiation of adjuvant chemotherapy, changes in physical fitness and quality of life, and relationships between biological markers and clinical outcomes.

Results from this study will establish the feasibility of implementing a personalised perioperative exercise programme for patients undergoing pancreatic cancer surgery and will provide essential data to inform the design of a future adequately powered multicentre randomised controlled trial evaluating the effectiveness of the ExO-PanC intervention.

研究类型

介入性

注册 (估计的)

60

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

  • 姓名:Tarak AM Chouari, BSc (Hons) MBChB
  • 电话号码:01483688691
  • 邮箱:t.chouari@nhs.net

学习地点

    • Surrey
      • Guildford、Surrey、英国、GU27XH
        • 招聘中
        • University of Surrey
        • 接触:
          • Tarak AM Chouari, BSc(Hons) MBChB
          • 电话号码:01483688691
          • 邮箱:t.chouari@nhs.net
        • 副研究员:
          • Tarak AM Chouari, BSc(Hons) MBChB
        • 首席研究员:
          • Adam E Frampton, PhD

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 成人
  • 年长者

接受健康志愿者

不

描述

Inclusion Criteria:

  • 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.

Exclusion Criteria:

  • <18 years age
  • 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
  • Not scheduled for surgery
  • A new diagnosis of Type 1 or Type 3c diabetes requiring management with insulin prescription will be excluded from the study.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:支持治疗
  • 分配:不适用
  • 介入模型:单组作业
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
实验性的:Intervention group
Participants will receive the ExO-PanC personalised exercise programme in addition to standard perioperative care. The intervention comprises four phases spanning the surgical pathway: prehabilitation before surgery, supervised inpatient exercise following surgery, structured home-based recovery after hospital discharge, and rehabilitation before commencement of adjuvant chemotherapy. Exercise is individually prescribed using cardiopulmonary exercise testing (CPET), muscle strength, and functional assessments, and includes aerobic and resistance with progression tailored to each participant's physical capacity. Participants also undergo repeated assessments of physical fitness, quality of life, nutritional status, and collection of blood, stool, and tumour tissue samples throughout the study.
Participants will receive the ExO-PanC personalised exercise programme alongside standard perioperative care. The intervention comprises four phases delivered across the surgical pathway: (1) prehabilitation before surgery, (2) supervised exercise during postoperative hospital admission, (3) structured home-based recovery following hospital discharge, and (4) rehabilitation before the commencement of adjuvant chemotherapy. Exercise prescriptions are individualised using cardiopulmonary exercise testing (CPET), muscle strength, and functional assessments. The programme includes aerobic, resistance, flexibility, and home-based exercise, with intensity and progression tailored to each participant's fitness level. Exercise may be delivered in supervised or semi-supervised formats, with heart rate monitoring used to support exercise prescription and progression. Participants continue to receive all standard NHS perioperative care throughout the study.

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Feasibility of the ExO-PanC exercise programme
大体时间:From enrolment until completion of the intervention (approximately 16-24 weeks)
Feasibility will be assessed using participant recruitment, adherence to the prescribed exercise programme (target >85% of prescribed sessions completed), compliance with prescribed exercise intensity, duration and type (target >80%), and participant retention (target <20% withdrawal for non-clinical reasons). Feasibility will be evaluated separately across the preoperative, perioperative and postoperative phases of the intervention.
From enrolment until completion of the intervention (approximately 16-24 weeks)

次要结果测量

结果测量
措施说明
大体时间
Postoperative surgical complications
大体时间:Up to approximately 6 weeks following surgery.
Occurrence and severity of postoperative complications, including pancreatic fistula and other clinically relevant surgical complications
Up to approximately 6 weeks following surgery.
Commencement and completion of adjuvant chemotherapy
大体时间:From surgery until planned commencement and completion of adjuvant chemotherapy.
Proportion of participants who commence planned adjuvant chemotherapy following pancreaticoduodenectomy and proportion who complete it
From surgery until planned commencement and completion of adjuvant chemotherapy.
Cardiorespiratory fitness (CRF) measured by cardiopulmonary excercise testing (CPET)
大体时间:Baseline through completion of the intervention (approximately 16-24 weeks)
Difference in anaerobic threshold (mL/kg/min) and peak oxygen uptake (VO₂peak, mL/kg/min) measured during CPET.
Baseline through completion of the intervention (approximately 16-24 weeks)
Muscle strength
大体时间:Baseline through completion of the intervention (approximately 16-24 weeks).
Changes in upper and lower body muscle strength measured using standardised strength assessments.
Baseline through completion of the intervention (approximately 16-24 weeks).
Change in health-related quality of life measured using the EORTC QLQ-C30
大体时间:Serial measurements from baseline through completion of the intervention (approximately 16-24 weeks).
Health-related quality of life assessed using the European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire Core 30 (EORTC QLQ-C30). Change in EORTC QLQ-C30 global health status, functional scales and symptom scales. Scores range from 0-100.
Serial measurements from baseline through completion of the intervention (approximately 16-24 weeks).
Nutritional status
大体时间:Baseline through completion of the intervention (approximately 16-24 weeks).
Nutritional status assessed using the Patient-Generated Subjective Global Assessment Short Form (PG-SGA SF).
Baseline through completion of the intervention (approximately 16-24 weeks).
Change in pancreatic cancer-specific quality of life measured using the EORTC QLQ-PAN26
大体时间:This will be measured at five timepoints from recruitment through to commencement of adjuvant chemotherapy
Serial changes in EORTC QLQ-PAN26 symptom scores. Scores range from 0-100.
This will be measured at five timepoints from recruitment through to commencement of adjuvant chemotherapy

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 首席研究员:Adam E Frampton, PhD、University of Surrey

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (估计的)

2026年7月6日

初级完成 (估计的)

2029年6月1日

研究完成 (估计的)

2030年6月1日

研究注册日期

首次提交

2026年7月6日

首先提交符合 QC 标准的

2026年7月13日

首次发布 (实际的)

2026年7月17日

研究记录更新

最后更新发布 (实际的)

2026年7月17日

上次提交的符合 QC 标准的更新

2026年7月13日

最后验证

2026年7月1日

更多信息

与本研究相关的术语

关键字

其他相关的 MeSH 术语

其他研究编号

  • 350182

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

是的

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

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