ExPO: Exercise Prior to Oesophagectomy

Sponsor
University of East Anglia (Other)
Overall Status
Unknown status
CT.gov ID
NCT02962219
Collaborator
(none)
32
1
2
19
1.7

Study Details

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.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Pre-operative Exercise Programme (my-PEP)
  • Behavioral: Home Exercise Programme (HEP)
N/A

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.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
32 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Prevention
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 Start Date :
Sep 1, 2016
Anticipated Primary Completion Date :
Sep 1, 2017
Anticipated Study Completion Date :
Apr 1, 2018

Arms and Interventions

Arm Intervention/Treatment
Experimental: Intervention

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

Behavioral: Pre-operative Exercise Programme (my-PEP)
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) .

Other: Control

Standard care

Behavioral: Home Exercise Programme (HEP)
Written advice on exercise at home

Outcome Measures

Primary Outcome Measures

  1. Recruitment rate [0 months]

    The number of participants recruited from all eligible patients

  2. Drop-out rate [12 months]

    Number of patients that drop-out from trial

  3. Decline rate [0 months]

    Number of patients that decline to participate in the trial

  4. Change in physical activity levels [0 and 4 months]

    Measured with International Physical Activity Questionnaire (IPAQ)

  5. Change in attitudes to exercise [0 and 4 months]

    Measured with Determinates of Physical Activity Questionnaire (DPAQ)

  6. Trial Adherence [12 months]

    Physical activity diary used to assess adherence

  7. Adverse Events [12 months]

    The number of adverse events during the trial assessed using CTCAE

  8. Change in physiological fitness [0 and 4 months]

    Assessed with maximal cardiopulmonary exercise test on a bicycle ergometer

  9. Change in respiratory muscle strength [0 and 4 months]

    Assessed with mean inspiratory pressure testing in cmH20

  10. Post-operative cardiopulmonary complications [90-days post surgery]

    Cardiopulmonary complication rates as per ECCG definition.

  11. Post-operative non-cardiopulmonary complications [90-days post surgery]

    Inpatient, 30-day and 90-day non-cardiopulmonary complication rates as per ECCG definition.

  12. Post-operative length of stay [90-days post surgery]

    Duration of post-operative stay in days

  13. Post-operative mortality [90-days post surgery]

    Number of post-operative deaths

  14. Change in Quality of Life [0, 4, 7 months]

    Assessed using QLQ C30 and OG25

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
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.

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of East Anglia Norwich Norfolk United Kingdom NR4 7TJ

Sponsors and Collaborators

  • University of East Anglia

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University of East Anglia
ClinicalTrials.gov Identifier:
NCT02962219
Other Study ID Numbers:
  • 206608
First Posted:
Nov 11, 2016
Last Update Posted:
Nov 11, 2016
Last Verified:
Nov 1, 2016
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Keywords provided by University of East Anglia
Additional relevant MeSH terms:

Study Results

No Results Posted as of Nov 11, 2016