The Effect of Novel High-intensity Interval Training on Physical Fitness in Older Adults

October 17, 2016 updated by: Christopher Hurst, Teesside University
High-intensity interval training (HIT) has been demonstrated to be an effective strategy to improve markers of health and fitness across a wide range of healthy and clinical populations. Currently however, there is only limited evidence which has examined the effectiveness of HIT in older adults (>50 years). HIT is an appealing strategy in this group as it has the potential to impact both cardiorespiratory and muscular fitness, which both play an important role in maintaining functional fitness and quality of life in a time-efficient manner. Developing an understanding of novel strategies for delivering this type of exercise training may ultimately provide a viable alternative to traditional modes of exercise training for a broader range of participants. As such, the purpose of this study is to evaluate the effects of a novel, high-intensity interval training exercise protocol to improve physical fitness in adults aged over 50 years. This research also aims to evaluate if this type of training intervention is feasible in this population, through analysis of adherence and intervention fidelity.

Study Overview

Status

Completed

Study Type

Interventional

Enrollment (Actual)

36

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Tees Valley
      • Middlesbrough, Tees Valley, United Kingdom, TS1 3BA
        • Teesside University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

50 years to 85 years (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  1. Must be aged 50-85 years
  2. Must be able to provide informed consent to participate
  3. Must be free from all exclusion criteria

Exclusion Criteria:

  1. Symptoms of or known presence of heart disease of major atherosclerotic cardiovascular disease
  2. Early family history of sudden cardiac death
  3. Condition or injury or co-morbidity affecting the ability to undertake exercise
  4. Diabetes mellitus
  5. Pregnancy or likelihood of pregnancy

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Intervention
Participants will undertake a high-intensity interval training intervention, completing two exercise sessions per week for 12 weeks. The exercise sessions will consist of 4 sets of 4-6 repetitions of 60s (45s high-intensity exercise, followed by 15s rest), interspersed with 3 minutes rest. During each exercise repetition participants will be encouraged to reach >90% of their maximal heart rate.
No Intervention: Control
Participants will not undertake any formal intervention and will be asked to maintain their usual physical activity habits and diet.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in lower body muscular power
Time Frame: Baseline and following exercise training (12 weeks)
Assessed via Nottingham Leg Extensor Power Rig
Baseline and following exercise training (12 weeks)
Change in Aerobic fitness
Time Frame: Baseline and following exercise training (12 weeks)
Assessed via Chester step test
Baseline and following exercise training (12 weeks)
Change in upper extremity muscular strength
Time Frame: Baseline and following exercise training (12 weeks)
Hand grip strength assessed using handheld dynamometer
Baseline and following exercise training (12 weeks)
Change in quality of life
Time Frame: Baseline and following exercise training (12 weeks)
Assessed via Short form quality of life questionnaire (SF36)
Baseline and following exercise training (12 weeks)

Other Outcome Measures

Outcome Measure
Time Frame
Heart rate during high-intensity interval training exercise sessions
Time Frame: Up to 12 weeks
Up to 12 weeks
Rating of perceived exertion (RPE) during high-intensity interval training exercise sessions
Time Frame: Up to 12 weeks
Up to 12 weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

April 1, 2016

Primary Completion (Actual)

August 1, 2016

Study Registration Dates

First Submitted

March 8, 2016

First Submitted That Met QC Criteria

March 15, 2016

First Posted (Estimate)

March 21, 2016

Study Record Updates

Last Update Posted (Estimate)

October 18, 2016

Last Update Submitted That Met QC Criteria

October 17, 2016

Last Verified

October 1, 2016

More Information

Terms related to this study

Other Study ID Numbers

  • TEES-CH170216-SSSBL

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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