NCT01859442

Brief Summary

The present study is a randomised control trial investigating the effects of a short six week exercise training program in rectal cancer patients following neoadjuvant chemoradiotherapy prior to elective rectal cancer surgery. Twelve patients will be randomised (1:1) to an intervention and a control group. The patients randomized to the intervention group will attend a total of 18 tailored exercise sessions (Three 40 minute sessions for six weeks) after their 6 weeks of chemoradiotherapy treatment. Where possible the exercise training sessions will be arranged to fit in with other appointments at the hospital. Patients randomized to the control group will be unsupervised. They will only attend an extra 3 sessions were a cardiopulmonary exercise test and VO2 Kinetics test will be performed. Patients will also be invited to attend 3 health related quality of life interviews at week 0, 3 and 6 during their exercise programme. These appointments will be directly before or after their exercise sessions to minimise hospital attendence. Following surgery only routine clinically relevant observational data will be collected. These data will relate to hospital length of stay, the level of care required following surgery, post-operative morbidity survey (POMS) and the recovery process. Most of this information can be accessed from patient notes and on the electronic patient records system. This is a subgroup RCT of patients in a larger interventional trial (6 control and 6 exercise intervention patients) will be asked to consent separately for the the 31-Phosphorus Magnetic Resonance Spectroscopy (31P MRS) scans and the blood samples. HYPOTHESIS

  1. 1.Interval exercise training will maintain or improve fitness (measured by anaerobic threshold) in patients undergoing neoadjuvant chemoradiotherapy.
  2. 2.Interval exercise training is safe and feasible in patients undergoing neoadjuvant chemoradiotherapy awaiting rectal cancer resection.
  3. 3.Interval exercise training will improve other measures of physical fitness measured in the CPET and the oxygen uptake kinetics test.
  4. 4.Interval exercise training will improve quality of life in patients undergoing neoadjuvant chemoradiotherapy.
  5. 5.Improvements in physical fitness will reduce postoperative complications following major rectal cancer surgery.
  6. 6.Does physical activity, measured by Sensewear Pro 3 activity monitors, decrease during neoadjuvant chemoradiotherapy and can this decrease be attenuated by an exercise training program?
  7. 7.Can we find an optimal time for surgery when fitness and cancer downstaging are at their best?
  8. 8.To explore the exponential rate constant of post-exercise phosphocreatine recovery.
  9. 9.To explore the alteration in cellular and mitochondrial energetics eg. Change in mitochondrial numbers, change in mitochondrial activity and respiration.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
12

participants targeted

Target at P25-P50 for early_phase_1

Timeline
Completed

Started Jan 2012

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 1, 2012

Completed
1.4 years until next milestone

First Submitted

Initial submission to the registry

May 13, 2013

Completed
9 days until next milestone

First Posted

Study publicly available on registry

May 22, 2013

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 1, 2013

Completed
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

October 1, 2013

Completed
Last Updated

May 6, 2014

Status Verified

September 1, 2013

Enrollment Period

1.5 years

First QC Date

May 13, 2013

Last Update Submit

May 5, 2014

Conditions

Outcome Measures

Primary Outcomes (1)

  • Exponential rate constant of post-chemoradiotherapy and post-exercise phosphocreatine recovery.

    Between baseline and week 0 and between week 0 at week 6 post-NACRT

Secondary Outcomes (1)

  • Alterations in mitochondrial energetics post-chemoradiotherapy and exercise

    Between baseline and week 0 and between week 0 and week 6 post-NACRT

Study Arms (2)

Exercise group

ACTIVE COMPARATOR

6 week structured responsive interval exercise training programme

Procedure: Structured responsive interval exercise training programme

Control group

SHAM COMPARATOR

Negative, unsupervised, out of hospital control group

Other: Sham group

Interventions

NO intervention in this group, only standard care (no exercise programme)

Control group

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • diagnosis of T3N+ rectal cancer
  • above age of 18
  • able to conduct a cardiopulmonary exercise test on a cycle ergometer

You may not qualify if:

  • unable to conduct a cardiopulmonary exercise test on a cycle ergometer
  • metastatic disease

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Aintree University Teaching Hospitals NHS FT

Liverpool, Merseyside, L97Al, United Kingdom

Location

Related Publications (1)

  • West MA, Loughney L, Lythgoe D, Barben CP, Adams VL, Bimson WE, Grocott MP, Jack S, Kemp GJ. The effect of neoadjuvant chemoradiotherapy on whole-body physical fitness and skeletal muscle mitochondrial oxidative phosphorylation in vivo in locally advanced rectal cancer patients--an observational pilot study. PLoS One. 2014 Dec 5;9(12):e111526. doi: 10.1371/journal.pone.0111526. eCollection 2014.

Study Design

Study Type
interventional
Phase
early phase 1
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
INVESTIGATOR, OUTCOMES ASSESSOR
Purpose
BASIC SCIENCE
Intervention Model
PARALLEL
Sponsor Type
OTHER GOV
Responsible Party
SPONSOR INVESTIGATOR
PI Title
Research an Developement Deputy Director

Study Record Dates

First Submitted

May 13, 2013

First Posted

May 22, 2013

Study Start

January 1, 2012

Primary Completion

July 1, 2013

Study Completion

October 1, 2013

Last Updated

May 6, 2014

Record last verified: 2013-09

Locations