search
Back to results

Exercise Prior to Oesophagectomy (ExPO)

Primary Purpose

Postoperative Complications (Cardiopulmonary), Oesophageal Adenocarcinoma

Status
Unknown status
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Pre-operative Exercise Programme (my-PEP)
Home Exercise Programme (HEP)
Sponsored by
University of East Anglia
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Postoperative Complications (Cardiopulmonary) focused on measuring oesophagectomy

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients with oesophageal adenocarcinoma (OAC) who are scheduled for neoadjuvant chemotherapy and subsequent oesophagectomy.
  • Must have histological evidence of OAC
  • Must be capable of giving informed consent and complying with trial procedures.

Exclusion Criteria:

  • Patients with oesophageal squamous cell carcinoma.
  • Patients with concomitant illness or disability that makes them unsuitable for an exercise programme, as determined by a clinician (e.g. severe musculoskeletal or neurological disease, unstable angina, severe aortic stenosis, uncontrolled dysrhythmias and uncompensated heart failure).
  • WHO performance status 3 (capable of only limited self-care, confined to a bed or chair more that 50% of waking hours) or greater.
  • Grade 5 (too breathless to leave the house, or breathless when undressing) on MRC dyspnoea scale.

Sites / Locations

  • University of East AngliaRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Other

Arm Label

Intervention

Control

Arm Description

A pre-operative personalised exercise programme (my-PEP).

Standard care

Outcomes

Primary Outcome Measures

Recruitment rate
The number of participants recruited from all eligible patients
Drop-out rate
Number of patients that drop-out from trial
Decline rate
Number of patients that decline to participate in the trial
Change in physical activity levels
Measured with International Physical Activity Questionnaire (IPAQ)
Change in attitudes to exercise
Measured with Determinates of Physical Activity Questionnaire (DPAQ)
Trial Adherence
Physical activity diary used to assess adherence
Adverse Events
The number of adverse events during the trial assessed using CTCAE
Change in physiological fitness
Assessed with maximal cardiopulmonary exercise test on a bicycle ergometer
Change in respiratory muscle strength
Assessed with mean inspiratory pressure testing in cmH20
Post-operative cardiopulmonary complications
Cardiopulmonary complication rates as per ECCG definition.
Post-operative non-cardiopulmonary complications
Inpatient, 30-day and 90-day non-cardiopulmonary complication rates as per ECCG definition.
Post-operative length of stay
Duration of post-operative stay in days
Post-operative mortality
Number of post-operative deaths
Change in Quality of Life
Assessed using QLQ C30 and OG25

Secondary Outcome Measures

Full Information

First Posted
October 28, 2016
Last Updated
November 8, 2016
Sponsor
University of East Anglia
search

1. Study Identification

Unique Protocol Identification Number
NCT02962219
Brief Title
Exercise Prior to Oesophagectomy
Acronym
ExPO
Official Title
A Pre-operative Personalised Exercise Programme to Improve Physical Fitness and Reduce Post-operative Cardiopulmonary Complications After Oesophagectomy in Patients With Oesophageal Adenocarcinoma: A Feasibility Randomised Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
November 2016
Overall Recruitment Status
Unknown status
Study Start Date
September 2016 (undefined)
Primary Completion Date
September 2017 (Anticipated)
Study Completion Date
April 2018 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of East Anglia

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this feasibility study is to determine whether a structured exercise programme prior to oesophagectomy has: acceptable adherence, is safe, and improves physiological measures of physical fitness above standard care.
Detailed Description
The number of patients with oesophageal cancer is rising dramatically in the UK. Curative cancer surgery (oesophagectomy) is offered to around 40% of affected patients. However, oesophagectomy is a major operation with a high risk of complications. Around 1 in 3 patients will suffer such a complication after surgery, mostly due to heart or lung problems. Most complications are not due to the surgery itself, but related to the patient's physical fitness before their operation. Studies in other surgeries, but not oesophagectomy, have shown that complications may be reduced by improving a patient's physical fitness before their operation. The ExPO team has developed a pre-operative Personalised Exercise Programme (my-PEP), specifically for patients undergoing oesophagectomy. my-PEP has 4 main components: three are exercise modalities (aerobic exercise, breathing exercises and muscle strengthening); the fourth is where a participant's potential barriers to exercise are assessed and behavioural change techniques (BCTs) are suggested to improve exercise engagement in the trial. In total, 32 patients who are due to undergo oesophagectomy at the Norfolk and Norwich Hospital will be recruited and then randomly divided into 2 arms of 16 each. One arm will receive my-PEP in the standard 3-4 months prior to surgery, the other will receive standard care advice to exercise at home. The research objectives are to obtain feasibility data on whether my-PEP is acceptable, adhered to and safe, and whether it improves patient fitness above standard care. Follow up will be 90 days after surgery to obtain a preliminary imprecise estimate of whether my-PEP reduces complications. If the ExPO trial shows promise in these areas, this will inform and justify a future large multi-centre trial to definitively answer whether my-PEP can reduce complications after oesophagectomy. If so, my-PEP could potentially change and improve the pre-operative management of oesophageal cancer patients across the NHS.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Postoperative Complications (Cardiopulmonary), Oesophageal Adenocarcinoma
Keywords
oesophagectomy

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
32 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Intervention
Arm Type
Experimental
Arm Description
A pre-operative personalised exercise programme (my-PEP).
Arm Title
Control
Arm Type
Other
Arm Description
Standard care
Intervention Type
Behavioral
Intervention Name(s)
Pre-operative Exercise Programme (my-PEP)
Intervention Description
A pre-operative personalised exercise programme (my-PEP) consisting of: 1) actions to promote exercise, using behavioural change techniques (BCTs), 2) home inspiratory muscle training (IMT), 3) a home exercise programme (HEP) - which is also current standard care, 4) a 4 week hospital-supervised aerobic and muscle strengthening programme (Hos-PEP) .
Intervention Type
Behavioral
Intervention Name(s)
Home Exercise Programme (HEP)
Intervention Description
Written advice on exercise at home
Primary Outcome Measure Information:
Title
Recruitment rate
Description
The number of participants recruited from all eligible patients
Time Frame
0 months
Title
Drop-out rate
Description
Number of patients that drop-out from trial
Time Frame
12 months
Title
Decline rate
Description
Number of patients that decline to participate in the trial
Time Frame
0 months
Title
Change in physical activity levels
Description
Measured with International Physical Activity Questionnaire (IPAQ)
Time Frame
0 and 4 months
Title
Change in attitudes to exercise
Description
Measured with Determinates of Physical Activity Questionnaire (DPAQ)
Time Frame
0 and 4 months
Title
Trial Adherence
Description
Physical activity diary used to assess adherence
Time Frame
12 months
Title
Adverse Events
Description
The number of adverse events during the trial assessed using CTCAE
Time Frame
12 months
Title
Change in physiological fitness
Description
Assessed with maximal cardiopulmonary exercise test on a bicycle ergometer
Time Frame
0 and 4 months
Title
Change in respiratory muscle strength
Description
Assessed with mean inspiratory pressure testing in cmH20
Time Frame
0 and 4 months
Title
Post-operative cardiopulmonary complications
Description
Cardiopulmonary complication rates as per ECCG definition.
Time Frame
90-days post surgery
Title
Post-operative non-cardiopulmonary complications
Description
Inpatient, 30-day and 90-day non-cardiopulmonary complication rates as per ECCG definition.
Time Frame
90-days post surgery
Title
Post-operative length of stay
Description
Duration of post-operative stay in days
Time Frame
90-days post surgery
Title
Post-operative mortality
Description
Number of post-operative deaths
Time Frame
90-days post surgery
Title
Change in Quality of Life
Description
Assessed using QLQ C30 and OG25
Time Frame
0, 4, 7 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients with oesophageal adenocarcinoma (OAC) who are scheduled for neoadjuvant chemotherapy and subsequent oesophagectomy. Must have histological evidence of OAC Must be capable of giving informed consent and complying with trial procedures. Exclusion Criteria: Patients with oesophageal squamous cell carcinoma. Patients with concomitant illness or disability that makes them unsuitable for an exercise programme, as determined by a clinician (e.g. severe musculoskeletal or neurological disease, unstable angina, severe aortic stenosis, uncontrolled dysrhythmias and uncompensated heart failure). WHO performance status 3 (capable of only limited self-care, confined to a bed or chair more that 50% of waking hours) or greater. Grade 5 (too breathless to leave the house, or breathless when undressing) on MRC dyspnoea scale.
Facility Information:
Facility Name
University of East Anglia
City
Norwich
State/Province
Norfolk
ZIP/Postal Code
NR4 7TJ
Country
United Kingdom
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Professor Andrew Hart
Phone
01603 593611
Email
a.hart@uea.ac.uk
First Name & Middle Initial & Last Name & Degree
Dr Stephen Lam
Phone
01603 286286
Email
stephen.lam@uea.ac.uk

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Exercise Prior to Oesophagectomy

We'll reach out to this number within 24 hrs