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HIT in the Healthy Elderly Population

Determining the Effectiveness of a High Intensity Interval Training Exercise Programme in the Healthy, Elderly Population

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02167191
Acronym
HIT
Enrollment
24
Registered
2014-06-18
Start date
2014-02-28
Completion date
2014-08-31
Last updated
2015-10-01

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

Conditions

Interval Training, Pre Operative Exercise, Prehabilitation, Elderly

Brief summary

It is widely known that exercise improves general fitness and that fitter patients recover more easily from illness and surgery. Conversely, unfit patients have a significantly higher morbidity and mortality after surgery and a longer inpatient stay. This will become increasingly important in an aging population as baseline fitness generally declines with age. One method of improving cardiovascular fitness is by using low intensity endurance training programmes, a disadvantage of these it that they can take several months to show improvement. High intensity interval training (HIT) programmes that use short episodes of high intensity exercise have also been shown to improve fitness. These HIT programmes have also shown improvement in functional capacity and quality of life in patients with chronic disease. An advantage of HIT is that improvements in fitness may occur in a shorter time than traditional endurance training. It is also known that HIT can give superior gains over endurance training. The primary aim of this study is to determine whether an improvement in aerobic fitness, as judged by a 2ml/kg/min increase in VO2peak, can be achieved within 31 days via a HIT programme, in a group of healthy elderly volunteers. As a secondary aim we will assess whether this programme would be acceptable to the group studied, through determination of subject compliance and adherence to the training programme.

Interventions

BEHAVIORALHIT

12 sessions of HIT exercise in 31 days on a stationary cycle ergometer

Sponsors

University of Nottingham
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
60 Years to 75 Years
Healthy volunteers
Yes

Inclusion criteria

* Good health * Male and female * 60 -75 years old

Exclusion criteria

* Uncontrolled hypertension (BP \> 140/100) * Angina * Heart failure (NYHA class III/IV) * Cardiac arrthymias * Right to left cardiac shunt * Recent cardiac event * Previous stroke/TIA * Aneurysm (large vessel or intracranial) * Severe respiratory disease including pulmonary hypertension * COPD/asthma with an FEV1 less than 1.5 l * Inclusion into any other research study in the last three months which involved: taking a drug; being paid a disturbance allowance; having an invasive procedure or exposure to ionising radiation

Design outcomes

Primary

MeasureTime frame
VO2 peak31 days

Countries

United Kingdom

Outcome results

None listed

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