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Preoperative HIIT in Elderly Cancer Patients

A Randomised Control Trial to Assess Efficacy of Preoperative High Intensity Interval Training in Elderly Patients Scheduled for Oncological Abdominal Surgery

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02671617
Acronym
eHIITCa
Enrollment
40
Registered
2016-02-02
Start date
2016-08-31
Completion date
2018-08-31
Last updated
2018-09-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cancer

Keywords

Abdominal Cavity, Aged

Brief summary

This randomized control trial will determine the effect of short term high intensity interval training (HIIT) on physical fitness, in an elderly patient group with active cancer, prior to surgical resection. Half of the recruited patients will act as a control group and the other half will undergo a HIIT protocol.

Detailed description

High intensity interval training (HIIT) has been shown to achieve similar and in some studies better improvements in aerobic fitness versus more traditional endurance based exercise over the same time period. HIIT has also been shown to produce these improvements over a shorter timescale than other methods, in the region of 2-6 weeks. One widely reported barrier to exercise is time availability, HIIT training may be a favorable option to increase fitness as the total time spent exercising is significantly less than other methods. HIIT induces improvements in cardiovascular parameters in healthy elderly subjects, investigators aim to investigate whether these improvements can be matched in patients with cancer and further elucidate the mechanisms behind improvements seen with this type of training.

Interventions

OTHERHigh intensity interval training (HIIT)

Preoperative HIIT protocol.

Sponsors

University of Nottingham
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
65 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Aged over 65 years (no upper age limit). * Histologically proven, radiologically or direct visualisation leading to high clinical suspicion of cancer. * Sufficient mobility to be able to exercise on a static exercise bike. * Ability to give informed consent. * Ability to travel to RDH to complete the HIIT sessions (may also rely upon dependents/relatives to provide transport).

Exclusion criteria

* Adjuvant systemic chemotherapy / radiotherapy treatment for this cancer. Participants with a significant past medical history of: * Myocardial infarction (within last 6 months) * Unstable Angina * Heart failure (NYHA class III/IV) * Uncontrolled Hypertension (BP\>160/100) * Previous stroke/TIA * Severe respiratory disease inc. known pulmonary hypertension(\>25 mmHg), Forced Expiratory Volume in 1 second \<1.5l. * Brittle asthma / exercise induced asthma * Known cerebral aneurysm. * Inclusion in a recent (within 3 months) study which included any form of exercise, taking a drug or ionising radiation.

Design outcomes

Primary

MeasureTime frameDescription
VO2AT (VO2 at anaerobic threshold)Baseline and 4 weeksChange in anaerobic threshold seen during maximal exercise test (pre and post intervention).

Secondary

MeasureTime frameDescription
VO2peakBaseline and 4 weeksChange in peak volume of oxygen consumption during maximal exercise test (pre and post intervention).
Subjective acceptability of HIIT preoperatively (via questionnaire)After 4 weeks of HIIT.Assessment of whether our HIIT protocol is acceptable to patients in this age group.
Muscle protein synthesis rate changes with HIIT.Baseline and 4 weeks.Assessment of the effect HIIT has on rate of muscle protein synthesis in this group.

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026